WO2008118808A1 - Liquid chromatography-mass spectrometry - Google Patents

Liquid chromatography-mass spectrometry Download PDF

Info

Publication number
WO2008118808A1
WO2008118808A1 PCT/US2008/057902 US2008057902W WO2008118808A1 WO 2008118808 A1 WO2008118808 A1 WO 2008118808A1 US 2008057902 W US2008057902 W US 2008057902W WO 2008118808 A1 WO2008118808 A1 WO 2008118808A1
Authority
WO
WIPO (PCT)
Prior art keywords
tube
column
mass spectrometer
analytes
analyte
Prior art date
Application number
PCT/US2008/057902
Other languages
French (fr)
Inventor
Gary A. Schultz
Reinaldo Rodrigo Queiros De Almeida
Mark Hayden Allen
Original Assignee
Advion Bioscience, Inc.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Advion Bioscience, Inc. filed Critical Advion Bioscience, Inc.
Publication of WO2008118808A1 publication Critical patent/WO2008118808A1/en

Links

Classifications

    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N30/00Investigating or analysing materials by separation into components using adsorption, absorption or similar phenomena or using ion-exchange, e.g. chromatography or field flow fractionation
    • G01N30/02Column chromatography
    • G01N30/80Fraction collectors
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N30/00Investigating or analysing materials by separation into components using adsorption, absorption or similar phenomena or using ion-exchange, e.g. chromatography or field flow fractionation
    • G01N30/02Column chromatography
    • G01N30/84Preparation of the fraction to be distributed
    • G01N2030/8447Nebulising, aerosol formation or ionisation
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N30/00Investigating or analysing materials by separation into components using adsorption, absorption or similar phenomena or using ion-exchange, e.g. chromatography or field flow fractionation
    • G01N30/02Column chromatography
    • G01N30/60Construction of the column
    • G01N30/6095Micromachined or nanomachined, e.g. micro- or nanosize
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N30/00Investigating or analysing materials by separation into components using adsorption, absorption or similar phenomena or using ion-exchange, e.g. chromatography or field flow fractionation
    • G01N30/02Column chromatography
    • G01N30/62Detectors specially adapted therefor
    • G01N30/72Mass spectrometers
    • G01N30/7233Mass spectrometers interfaced to liquid or supercritical fluid chromatograph
    • G01N30/724Nebulising, aerosol formation or ionisation
    • G01N30/7266Nebulising, aerosol formation or ionisation by electric field, e.g. electrospray

Definitions

  • This description relates to method and system for liquid chromatography-mass spectrometry (LC/MS) analyses of biological analytes such as proteins and/or peptides, and more particularly to data dependent nano-LC/MS acquisitions.
  • LC/MS liquid chromatography-mass spectrometry
  • Liquid chromatography is a well-established analytical technique for separating components of a fluidic mixture for subsequent analysis and/or identification, in which a column, micro fluidic chip-based channel, or tube is packed with a stationary phase material that typically is a finely divided solid or gel such as small particles with diameter of a few microns. ' Hie small particle size provides a large surface area that can be modified with various chemistries creating a stationary phase.
  • a liquid elucnt is pumped through the liquid chromatographic column ("LC column”) at a desired flow rate based on the column dimensions and particle size. This liquid elucnt is sometimes referred to as the mobile phase.
  • the sample to be analyzed is introduced (e.g., injected) in a small volume into the stream of the mobile phase prior to the LC column.
  • the analytes in the sample are retarded by specific chemical and/or physical interactions with the stationary phase as they traverse the length of the column.
  • the amount of retardation depends on the nature of the analytc, stationary phase and mobile phase composition.
  • the time at which a specific analyte elutes or comes out of the end of the column is called the retention time or elution time and can be a reasonably identifying characteristic of a given analytc especially when combined with other analyzing characteristics such as the accurate mass of a given analyte.
  • the analytes interact with the stationary phase based on the partition coefficients for each of the analytes.
  • the partition coefficient is defined as the ratio of the time an analyte spends interacting with the stationary phase to the time spent interacting with the mobile phase. The longer an analyte interacts with the stationary phase, the higher the partition coefficient and the longer the analytc is retained on the LC column.
  • An isocratic flow in LC describes a mobile phase of a constant composition. In contrast to this is the so called "gradient clution", which is a separation where the mobile phase composition changes during a separation process. For example, a 20-minutc gradient starts from 10% MeOH and ends up with 30% McOH within 20 minutes.
  • Detection of analytcs separated on an LC or nanoLC column can be accomplished by use of a variety of different detectors. Spectroscopic detectors rely on a change in refractive index, ultraviolet and/or visible light absorption, or fluorescence after excitation with a suitable wavelength to detect the separated components. Additionally, the separated components may be passed from the liquid chromatographic column into other types of analytical instruments for further analysis, e.g., liquid chromatography-mass spectrometry (LC/MS or LC-MS) separates compounds chromatographically before they arc introduced to the ion source of a mass spectrometer.
  • LC/MS liquid chromatography-mass spectrometry
  • the purpose of the LC column is to separate analytes such that a unique response (e.g., a UV absorption peak) for each analyte from a chosen detector can be acquired for a quantitative or qualitative measurement.
  • the ability of a LC column to generate a separation is determined by the dimensions of the column and the particle size supporting the stationary phase.
  • the retention time of an analyte can be adjusted by varying the mobile phase composition and the partition coefficient for an analyte. Increases in chromatographic separation can be achieved via a reduction in the LC column diameter, increasing LC column length and/or a reduction of stationary phase particle dimensions.
  • Mass spectrometry is an analytical technique used to measure the mass-to-charge ratio of gas phase ions. This is achieved by ionizing the sample and separating ions of differing masses and recording their relative abundance by measuring intensities of ion flux.
  • a typical mass spectrometer comprises three parts: an ion source, a mass analyzer, and a detector system.
  • the ion source is the part of the mass spectrometer that ionizes the substance under analysis (the analyte).
  • the ions arc then transported by magnetic or electric fields to the mass analyzer that separates the ions according to their mass-to-charge ratio (m/ ⁇ ).
  • Mass spectrometers use two or more mass analyzers for tandem mass spectrometry (MS/MS).
  • the detector records the charge induced or current produced when an ion passes by or hits a surface.
  • a mass spectrum is the result of measuring the signal produced in the detector when scanning m/z ions with a mass analyzer.
  • Mass spectrometry has rapidly developed as an important emerging method for the characterization of proteins.
  • the two primary methods for ionization of whole proteins arc elcctrospray ionization (ESl) and matrix-assisted laser desorption/ionization (MALDI).
  • ESl elcctrospray ionization
  • MALDI matrix-assisted laser desorption/ionization
  • proteins are ionized by either of the two techniques described above, and then introduced to a mass analyzer.
  • proteins arc cnzymatically digested into smaller peptides using an agent such as trypsin or pepsin.
  • the collection of peptide products are then introduced to the mass analyzer.
  • the latter is often referred to as the "bottom-up" approach of protein analysis.
  • Proteins and/or peptides ⁇ f interest to biological researchers are usually part of a very complex mixture of other proteins and molecules that co-exist in the biological medium.
  • the high complexity of biological mixtures often makes coupling a separation technique, such as high performance liquid chromatography (HPLC), highly desirable or even required after enzymatic digestion.
  • HPLC high performance liquid chromatography
  • HPLC on-line connected to ESI-MS offers the possibility for pre-conccntration of dilute samples, desalting and removal of detergents.
  • improving detection sensitivity can become especially important. Improvement of detection sensitivity using concentration sensitive detectors such as UV/Vis absorbance and ESI mass spectrometers can be achieved by employing HPLC columns with smaller internal diameters (i.d.). For example, increased sensitivity during peptide analysis can result from using nano-LC (e.g., column i.d. of 50-100 ⁇ m) and capillary LC (e.g., column i.d. of 320 ⁇ m).
  • Flow rate of the mobile phase through such columns is from several nanoliters per minute (nL/min), to several microliters per minute ( ⁇ L/min), and the mobile phase can be sprayed directly without post- column splitting.
  • nL/min nanoliters per minute
  • ⁇ L/min microliters per minute
  • Elcctrospray ionization or nanoESI is a commonly applied ionization technique when dealing with biomolccules such as peptides and proteins.
  • the electrospray process creates highly-charged droplets that, under evaporation, create ions representative of the species contained in the solution.
  • An ion-sampling orifice of a mass spectrometer may be used to sample these gas phase ions for mass analysis.
  • a conducting needle (often referred to as a sprayer or emitter) relative to an extracting electrode, such as one provided at the ion-sampling orifice of a mass spectrometer
  • the electric field generated on the needle causes the separation of positively and negatively charged ions in solution and pushes ions of one polarity (e.g., positively charged or negatively charged) to the solution surface.
  • a volume of the fluid is pulled into the shape of a cone, known as a Taylor cone, which extends from the tip of the needle.
  • a liquid jet extends from the tip of the Taylor cone and becomes unstable and generates charged-droplcts.
  • These small charged droplets are drawn toward the extracting electrode, e.g., the sampling electrode of a mass spectrometer.
  • the small droplets are highly- charged and solvent evaporation from the droplets results in the excess charge in the droplet residing on the analyte molecules in the electrosprayed fluid.
  • the charged molecules or ions are drawn through the ion-sampling orifice of the mass spectrometer for mass analysis.
  • V potential voltage required to initiate an elcctrospray is dependent on the size of the sprayer, the surface tension of the solution, and the electric field can be on the order of approximately I O 6 V/m.
  • the physical si/.e of the needle and the fluid surface tension determines the density of electric field lines necessary to initiate electrospray.
  • the sample is sprayed from a needle with a tip diameter less than about 5 ⁇ m, using a sample flow rate between 5 nL/min and 50 nL/min, for example.
  • Charged droplets with diameters less than 1 micron can be formed at flow rates less than 40 nL/min.
  • NanoESl-MS can thus be used for analyzing small amounts of sample with low sample concentrations (e.g., fcmtomolc/microlitcr).
  • sample concentrations e.g., fcmtomolc/microlitcr.
  • the ion response for analytes contained in a sample solution is proportional to its concentration instead of its total amount. What this means is that if a solution is being sprayed at 200 nL/min or 50 nL/min or 20 nL/min the signal intensity as measured using mass spectrometry would be the same.
  • mass spectrometry By reducing a flow rate by a factor of 5 roughly increases mass spectrometry scans to be acquired for the same amount of sample by a factor of 5.
  • signal averaging from the increased number of scans improves signal-to-noisc ratios and ion statistics which enable multiple MS/MS experiments on the analytes and high accuracy in identifying analytcs.
  • Tandem mass spectrometry is a popular experimental method for identifying biomolecules such as proteins. Tandem MS involves multiple steps of mass selection or analysis, usually separated by some form of fragmentation.
  • a tandem mass spectrometer is capable of multiple stages of mass spectrometry. For example, one mass analyzer can isolate one peptide from many others entering a mass spectrometer. A second mass analyzer then stabilizes the peptide ions while they collide with a gas, causing them to fragment by collision- induced dissociation (CID). A third mass analyzer then characterizes the fragments produced from the peptides. Tandem MS can also be done in a single mass analyzer over time as in a quadrup ⁇ le i ⁇ n trap.
  • CID collision-induced dissociation
  • ECD electron capture dissociation
  • ETD electron transfer dissociation
  • IRMPD infrared multiphoton dissociation
  • BIRD blackbody infrared radiative dissociation
  • HPLC/MS is also called shotgun proteomics. Shotgun analysis involves direct digestion of protein mixtures to complex peptide mixtures, followed by the automated identification of the peptides by liquid chromatography combined with tandem mass spectrometry (LC-MS/MS).
  • LC-MS/MS tandem mass spectrometry
  • Modern mass spectrometers with data dependent scanning software are capable of acquiring MS and MS/MS data from many hundreds of peptides per hour.
  • the principle of shotgun analysis is to first "spread out" peptides in complex mixtures by multidimensional chromatographic separation. Tandem MS instruments then acquire peptide MS/MS spectra, which encode the peptide sequences. This acquisition can be done in a data-dependent way, whereby the instrument relics on a preliminary scan, performed as the peptides enter the instrument, to select peptides for fragmentation and generation of MS/MS spectra.
  • a liquid chromatography system includes: a chromatographic column through which an effluent passes, wherein the effluent comprises a plurality of analytcs that correspond to a plurality of chromatographic peaks and an eluent; a post-column splitter having at least two output ports through which the effluent of the column is split to at least a first portion and a second portion; a mass spectrometer configured to receive the first portion from a first of the output ports for analysis; and a tube connected to a second of the output ports configured to prevent substantial evaporation of the eluent in the second portion until undergoing mass spectrometry.
  • the second portion has a plurality of separated analytes corresponding to at least two chromatographic peaks.
  • aspects can include one or more of the following features.
  • the system is configured to direct the second portion to the mass spectrometer after the first portion is analyzed by the mass spectrometer.
  • the system further comprises a pump connected to the tube to pump the second portion to the mass spectrometer after the first portion is analyzed by the mass spectrometer.
  • Hie system further comprises a second detector configured to receive the second portion irom the tube after the first portion is analysed by the mass spectrometer.
  • the second detector comprises a mass spectrometer.
  • the second detector comprises an infusion nanoESI/MS device.
  • the tube is configured to substantially reduce the diffusion of the analytes in the effluent stored in the tube.
  • the tube is configured to stay at a temperature lower than the room temperature.
  • the tube comprises an electrolysis electrode to elcctrolyze the eluent to produce a gas segment between any two eluent segments.
  • the electrolysis is triggered by an analytical device.
  • the device is an ultraviolet detector, fluorescence detector, an electrochemical detector, evaporative light scattering detector, nuclear magnetic resonant spectrometer, charged aerosol detector, refractive index detector, or a mass spectrometer.
  • the mass spectrometer comprises an clectrospray sprayer.
  • the mass spectrometer comprises an ESI/MS device.
  • the mass spectrometer comprises an infusion nanoESI/MS device.
  • the infusion nanoESI/MS device comprises a nanoESI sprayer.
  • the nanoESI sprayer comprises a pulled tip of a fused silica capillary.
  • the infusion nanoESI/MS device comprises a chip containing an array of nanoclcctrospray nozzles.
  • the tube comprises a fused silica capillary.
  • the tube has a diameter of 250 ⁇ m or less.
  • the tube has a diameter of 100 ⁇ m or less.
  • the tube has a diameter of 75 ⁇ m or less.
  • the tube has a diameter of 50 ⁇ m or less.
  • the tube has a length of about 1 meter or more.
  • the tube has a length of about 10 meters or less.
  • the tube has a length of about 6 meters.
  • the second portion is directed for mass spectrometry at a lower flow rate than the first portion is.
  • the splitter comprises a T-shape piece that creates a volume ratio of about 4: 1 to about
  • the splitter comprises a valve that has at least five ports, a first connector connecting two of said ports, and a second connector connecting three or more of the rest said ports to split the effluent.
  • the valve has at least six ports.
  • the valve has at least one port connected to a flow controller.
  • the valve has two ports that arc connected by the tube.
  • the valve is switchable between at least two configurations, including a first configuration in which the second connector connects a first set of three ports, and a second configuration in which the second connector connects a second set of ports different from the first set.
  • ITic analytes in the second portion exit the tube in the same order in which the analytcs exit the chromatographic column.
  • the analytes in the second portion exit the tube in a reversed order in which the analytes exit the chromatographic column.
  • the second portion is mixed with a stream of liquid before the portion undergoes mass spectrometry.
  • the second portion has a plurality of separated analytes corresponding to at least half of the plurality of chromatographic peaks corresponding to the analytes that pass through the chromatographic column.
  • the second portion has a plurality of separated analytes corresponding to at least 90% of the plurality of chromatographic peaks corresponding to the analytes that pass through the chromatographic column.
  • the system further comprises a second chromatographic column, wherein the inner diameter of the second column is smaller than that of the first column.
  • a method of characterizing an analyte in a sample includes: passing an effluent comprising a plurality of analytes and an eluent through a chromatographic column, the analytes corresponding to a plurality of chromatographic peaks; splitting at least a first portion and a second portion of the effluent from respective output ports of a post-column splitter, the first portion being directed from a first of the output ports to a mass spectrometer for analysis; and receiving the second portion having a plurality of separated analytes corresponding to at least two chromatographic peaks in a tube connected to a second of the output ports to prevent substantial evaporation of the eluent before undergoing mass spectrometry.
  • the method further comprises directing the second portion irom the tube to the mass spectrometer after the first portion is analyzed by the mass spectrometer.
  • the method further comprises directing the second portion from the tube to a second mass spectrometer after the first portion is analyzed by the mass spectrometer.
  • the method further comprises analyzing a first analyte from the stored second portion after a second analyte from the first portion has been analyzed by the mass spectrometer, wherein the first analyte passed out of the chromatographic column before the second analyte passed out of the chromatographic column.
  • the method further comprises analyzing a first analyte from the stored second portion after a second analyte from the second stored portion has been analyzed by the mass spectrometer, wherein the first analyte passed out of the chromatographic column before the second analyte passed out of the chromatographic column.
  • the method further comprises analyzing a first analyte from the stored second portion before a second analyte from the second stored portion has been analyzed by the mass spectrometer, wherein the first analyte passed out of the chromatographic column before the second analyte passed out of the chromatographic column.
  • the method further comprises cooling the second portion to substantially reduce diffusion of the analytcs in the elucnt captured in the tube.
  • the method further comprises segmenting the stored second portion into a least two segments in the tube by a gas bubble wherein the gas bubble creates a diffusion boundary to the analytcs in the portion.
  • the gas bubble is formed by electrolysis of the eluent of the second portion.
  • the method further comprises recording the segment positions in the tube by counting gas bubbles.
  • the method further comprises segmenting the stored second portion into at least two segments in the tube by a non-mixing liquid segment wherein the non-mixing liquid segment creates a diffusion boundary to the analytes in the portion.
  • the method further comprises directing the stored second portion in the rube to the mass spectrometer at a calibrated ilow rate controlled by a pump connected to the tube.
  • the calibrated flow rate is less than 5,000 nL/min.
  • the calibrated flow rate is less than 1 ,000 nL/min.
  • the calibrated flow rate is less than 200 nL/min.
  • the second portion has a plurality of separated analytcs corresponding to at least half of the plurality of chromatographic peaks corresponding to the analytes that pass through the chromatographic column.
  • the second portion has a plurality of separated analytcs corresponding to at least 90% of the plurality of chromatographic peaks corresponding to the analytes that pass through the chromatographic column.
  • the method further comprises directing the effluent into a second chromatographic column.
  • the directing is performed by controlling back pressures of the splitter by connecting a pump to a port of the splitter.
  • a post-column splitter can divide a liquid chromatographic effluent such that a first fraction of the effluent is subjected to immediate nanoclectrospray mass spectrometry analysis while a second fraction is captured and stored in a tube, e.g., a capillary tube with i.d. of about a few tens of microns.
  • the splitter can be a T-shapc piece, or chip-based channels, or a multi- port valve that can divide the effluent.
  • the splitter can also be configured to divide the effluent to more than two fractions thus allow more than one fractions to be captured and stored in individual tubes for later usage.
  • the dimension of the capture tube is selected to control diffusion of analytcs molecules so that the degree of remixing of the separated analytcs can be controlled or minimized.
  • Gas segments can be introduced to the captured fraction to further limit diffusion of LC-separated analytes to confined regions and thus greatly increase storing time of the faction.
  • using a tube to store a fraction of the LC effluent allows the analytc molecules maintained in a solution, e.g., to prevent decomposition of the analyte upon drying or to prevent loss of precious sample by drying and redissolving it in a solvent.
  • the second fraction collected in the tube can be redirected to a nanoESl sprayer to enable additional MS data to be acquired from the same sample injection based on the initial MS analysis of the first fraction, e.g., at a lower flow rate to the sprayer for targeted analytes or skipping analysis oiTcss interesting analytcs in the fraction to save time.
  • the captured fraction can also be modified or treated before MS analysis by, e.g., adding another solvent, or undergoing another LC analysis, e.g., ion exchange chromatography.
  • FIG I A is a simplified cross-sectional schematic of a LC/MS system.
  • FIG. I B is a cross-sectional schematic of an embodiment.
  • FIGS. 2 A and 2B are schematics of a LC/MS system.
  • FIGS. 3A-G arc schematics of another embodiment.
  • FIG. 4 is a cross-sectional view of an embodiment of a capture tube.
  • FIGS. 5 A and 5B are schematics of still another embodiment.
  • FIGS. 6A-C arc schematics of yet another embodiment.
  • FIGS. 7A-C arc schematics of embodiments with a capture capillary.
  • Liquid chromatography with columns of small internal diameters, e.g., capillary LC and nano-LC columns, can be coupled with nanoESI to combine the benefits of sample separation and/or concentration in columns of small diameters and improved ionization efficiencies with nanoESl.
  • peak widths should be narrow, but narrow peaks limit the acquisition time for mass spectral data.
  • an analytical system should enable separation of all compounds within an HPLC system (narrow peaks and high peak capacity), while enabling essentially unlimited time to acquire mass spectrometric data for each separated compound.
  • peak width at half height of compounds cluting from capillary- or nano-LC columns is generally in the range of 5 seconds to 30 seconds.
  • the peptide needs to be sequenccd, which may require multiple stages of MS detection. Sequencing of the peptides is performed by compa ⁇ ng measured and calculated fragment spectra. These scan cycles take approximately a few hundred milliseconds to a few seconds, which allows the experiment to perform only limited numbers of cycles during the clution of a chromatographic peak.
  • Some nano-LC/nanoESI-MS techniques spray the entire effluent exiting the nano-LC column with a nanoESI sprayer.
  • each analytc cluting from a column occurs as a transient with a time profile of seconds.
  • data-dependent scanning or other methods of MS/MS such as ECD or ETD may not be able to acquire spectra fast enough to identify all the analytes, e.g., peptides, as they enter the MS instrument, thus many analyte identifications can be missed.
  • the strengths of nano liquid chromatography/mass spectrometry (nanoLC/MS) and infusion nanoelectrospray mass spectrometry (nanoESI/MS) can be combined with a post-column splitter that divides die LC effluent such that a first portion or fraction of the effluent is subjected to nanoelectrospray mass spectrometry analysis immediately after chromatographic separation and a second portion or fraction is captured and stored in a tube, e.g., a capillary tube with i.d. of about 20 - 50 ⁇ m.
  • the second portion collected in the tube can be redirected to a nanoESl sprayer to enable additional MS data to be acquired from the same sample injection based on the initial MS analysis to allow more signal averaging and improve accuracy of sample identification or protcome coverage in a shotgun experiment, for instance.
  • an LC/MS system 10 includes a liquid chromatographic column 12, e.g., a nano-LC column, which provides on-line separation capabilities to mass spectral analysis of the effluent 20 containing a plurality of separated analytes (illustrated as squares, circles, crosses, and triangles).
  • a portion 24 of the effluent 20 is directed via some tubing 19 (e.g., a capillary tube) to mass spectrometer or MS device 18, e.g., a nanoESI/MS device.
  • Another portion 22 of the effluent 20 is simultaneously captured and stored in a tube 16 which is configured to control (e.g., to reduce) the diffusion of the analytes in the effluent inside the tube 16 and substantially preserve the chromatographic separation of analytes from the column 12.
  • ' ITic effluent 20 is split by a post-column splitter 14 to at least two portions 22 and 24.
  • the portion 22 of the effluent can, in some cases, keep entering tube 16 and keep moving along in tube 16. Or 1 in other cases in which it may be desirable to store the portion 22 for longer periods of time, the portion 22 can be kept substantially stationary in tube 16 for a period of time that is long enough for the MS device 18 to further analyze the portion 24.
  • the portion 22 can be redirected through the tube 16 and the splitter 14 to the MS device 18 (or redirected to a different MS device) for a second round of analysis, e.g., tandem MS.
  • tubing 19, splitter 14, and/or the tube 16 can be integrated into a microfluidic chip, e.g., a chip containing a splitter connected to a long channel (e.g., a microfluidic channel) functioning as tubing 19 and/or tube 16.
  • a microfluidic chip e.g., a chip containing a splitter connected to a long channel (e.g., a microfluidic channel) functioning as tubing 19 and/or tube 16.
  • column 12 can be an HPLC column with an internal diameter in the micrometer scale, e.g., a nano-LC column of 75 ⁇ m i.d., and the flow rate can be controlled by a nano-LC pump to range between about 10 nL/min to 1000 nL/min, e.g., about 200 nL/min to 300 nL/inin.
  • the post-column splitter 14 can be a T-shape piece ("Tee") as shown in FlG 1 B.
  • the T-shape piece includes an input port 1 1 which can be connected to an outlet of the nano-LC column, two output ports 13 and 15 which divides the LC effluent 20 entering the Tee into two portions (shown as portion 24 to MS device and portion 22 to capture tube), and an air tight fitting 17 which holds the three ports together and allows fluid communication between the ports.
  • Each of the two output ports can be an integral part of the tubing or tube that the two split portions enter respectively, e.g., port 13 can be the proximal end of tubing 19 (in FlG I A) and port 15 can be the proximal end of tube 16 (in FIG IA) with respect to the flow direction.
  • the split ratio usually the flow rate ratio of the two portions 24 and 22, e.g., portion to be analyzed vs. portion to be stored, can be adjustable from 1 : 100 to 10: 1 , e.g., from 1 : 10 to 5: 1 , from 1 :3 to 4: 1 , from 1 : 1 to 3: 1 , according to different experimental needs. For example, if flow rate of portion 24 is required to be 50-100 nL/min, when the flow rate of the LC effluent is 200 nL/min, the flow rate ratio would be selected to be 1 :3 to 1 : 1.
  • the flow rate ratio can be adjusted by controlling the back pressures of the output ports of the splitter.
  • back pressure can be adjusted by controlling the back pressures of the output ports of the splitter.
  • the inner diameters of the output ports and/or the tubes connected to them can be about 5 ⁇ m to 750 ⁇ m, e.g., 10 to 500 ⁇ m, 20 to 200 ⁇ m, or 50 to 100 ⁇ m.
  • port 13 can have 15 ⁇ m i.d. with 15 centimeters of total tubing length while port 15 has 50 ⁇ m i.d. with 600 cm of total tube length to achieve a flow rate ratio of 1 :3.
  • Back pressure can also be affected by applying external pressure to the split portions via, e.g., a spit adjustor, more detail of which follows.
  • an LC/MS system 10 can further include an autosamplcr 30 upstream of the LC column 12.
  • the mobile phase or the eluent for LC is driven by a pump 40 which can also adjust the flow rate of mobile phase on the order of nL/min.
  • the arrows in FIGS. 2A and 2B indicate flow directions of the mobile phase.
  • the system 10 can switch between a first "online LC/MS plus splitting” mode (FlG 2A) and a second "no- splitting infusion” mode (FlG 2B) via use of a multiple port valve, e.g., a micro switching valve 60 having six ports labeled 1 through 6 with every port conncctable to either one of the two neighboring ports through a connector such as a groove or channel (not shown but connection is illustrated by arrows or lines between each two ports) in the valve.
  • a multiple port valve e.g., a micro switching valve 60 having six ports labeled 1 through 6 with every port conncctable to either one of the two neighboring ports through a connector such as a groove or channel (not shown but connection is illustrated by arrows or lines between each two ports) in the valve.
  • a multiple port valve e.g., a micro switching valve 60 having six ports labeled 1 through 6 with every port conncctable to either one of the two neighboring ports through a connector such
  • ports 5 and 6 of valve 60 arc in fluid communication so that the pump 40 can drive the mobile phase to carry the sample from the autosampler through the LC column 12 then through post-column splitter 14.
  • a first portion of the effluent of column 12 is directly driven to the mass spectrometer 18 while a second portion is captured by a tube 16.
  • a device 50 is connected to port 3 of the valve 60.
  • the device 50 can be a waste or a split adjustor for, e.g., controlling the flow rate of the captured portion in tube 16.
  • the device 50 can be a second mass spectrometer, e.g., a nanoESI/MS device to analyze the captured portion based on the analysis results from the first portion.
  • ports 5 and 4 of valve 60 arc in fluid communication so that the pump 40 can drive the captured portion of LC effluent back to the splitter 14 then to MS device 18 where the order of analytcs in the captured portion entering the MS device is reversed due to this set up configuration, i.e., the first into the tube will be the last out for MS analysis.
  • the back pressure of column 12 can prevent the captured portion flowing back to the LC column.
  • a closing valve might be used between column 12 and splitter 14 to prevent the back flow to column 12. The selection between the two modes can either be manually or automatically controlled.
  • the timing of switching from one mode to another can be experiment specific. For example, one can switch system 10 from the first mode to the second only after all components of the sample has been LC separated and elutcd; or one can do so intermittently by pausing the LC separation when it is necessary.
  • the captured effluent portion may be directed to another analytical device or another mass spectrometer, e.g., another nanoESI/MS.
  • splitter 14 can be a multiple-port micro switching valve with at least one groove or channel that connects three or more ports simultaneously so that the valve can not only exhibit the same function as a T-shape splitter but also have additional functional features.
  • a 6-port valve is shown in FIGS. 3A through 3F. Arrows in these figures indicate flow directions of the analytes.
  • valve 14 is in the 'splitting and capture' mode, and unlike in a conventional switching valve, port 6 is connected to both of its two neighboring ports (ports 1 and 5) through a groove or channel of the valve as well as connected to an outlet of the LC column 12 simultaneously so that the effluent from column 12 can be split into two portions with one flowing to the MS device 18 while the other flowing into a capture tube 16 connecting ports 5 and 2.
  • Ports 2 and 3 are connected through another groove or channel of the valve in this mode.
  • Port 3 is also connected to a split adjuster 50 to adjust the nanoLC split ratio, e.g., the flow rate ratio of port 1 to port 5, while port 4 is isolated from the other ports.
  • the split adjuster can either be a pressurized vessel or a pump, which is used to adjust the back pressure of the tube 16 in order to control the split ratio, as discussed above.
  • valve 14 is switched to the 'infusion' mode.
  • the groove that connected port 6 to ports 1 and 5 in the 'splitting and capture' mode now rotates counterclockwise so that port 5 is connected to both of its neighboring ports (ports 4 and 6) simultaneously while the groove that connected ports 2 and 3 now connects ports 1 and 2.
  • the resulting configuration is then port 6 connected to the pump 40 through column 12 and port 2 connected to port 1 so that the captured portion of separated analytes in tube 16 between ports 5 and 2 can be driven by the mobile phase of column 12 into the MS device 18 through port 1.
  • the flow rate of the mobile phase is controlled by pump 40.
  • port 4 can connect to a split adjuster 50 to adjust the flow rate of the captured portion entering MS device 18 without having to decrease the flow rate of the mobile phase in LC column 12.
  • the flow rate in LC column can be kept at 200 nL/min while the flow rate in tube 16 can be adjusted to 50 nL/min by bifurcating the mobile phase exiting the LC column at port 5 with about three fourths of the mobile phase flowing to port 4 with the assistance of the split adjuster 50.
  • the captured effluent portion may be directed to another analytical device or another mass spectrometer, e.g., another nanoESI/MS.
  • the flow for infusion nanoESI/MS of the captured chromatogram can be driven by the column wash in the column regeneration steps thereby enabling simultaneous infusion experiment and column preparation for the next injection which leads to an improvement in speed and efficiency of the analytical process, for example.
  • the grooves in the valve connecting neighboring ports have a width of about 10-150 ⁇ m and a depth of about 5-75 ⁇ m.
  • the valve structure of splitter 14 enables the order of the analytes in the captured portion entering the MS device to be the same order of exiting the LC column, i.e., the first into the capture tube will be the first out for MS analysis.
  • valve configuration One potential benefit of using this valve configuration is that the analytes or components captured into the tube each go in one end and out the other, thereby traversing the same length and arc subjected to a similar degree of diffusion so that the chromatographic peaks have similar degree of broadening.
  • composition modification or treatment of the captured portion of the separated analytes in tube 16 may be desired, e.g., adding a different mobile phase to increase ionization of the analytes for mass spectrometry experiment.
  • the modification of the captured portion may achieve, e.g., changes in ionization, electrochemical modification of captured components, enzyme degradation of intact proteins or peptides, mass tagging, or enzymatic de-phosphorylation of peptides or proteins, thus providing additional assistance in sample characterization.
  • FIGS. 3C-3D and 3E-3F Two exemplary approaches of introducing a 'treating' flow of, e.g., a compound, a rcactant to a given analyte, a salt, and/or a mobile phase, to the captured portion in tube 16 are illustrated in FIGS. 3C-3D and 3E-3F, namely the 'prc-tubc' and 'post-tube 1 approaches.
  • the 6-port switch valve has an additional groove that connects ports 4 and 5 compared to the valve in its 'splitting and capture' mode as illustrated in FlG 3A.
  • Port 4 also connects to an ancillary control device 90 to add the 'treating' flow to the captured portion of the LC effluent at the entrance (i.e. port 5) of the tube 16.
  • Device 90 may be a stock solution connected to a pump which can control the flow rate of the solution adding to the captured portion.
  • the split adjuster 50 connected to port 3 can control the split ratio of the LC effluent.
  • valve is in its 'infusion' mode.
  • the additional groove that connected ports 4 and 5 in FIG 3C rotates counterclockwise and now connects ports 4 and 3.
  • port 3 can optionally connect to split adjuster 50 to control the flow rate of the captured portion entering a mass spectrometer.
  • the 6-port switch valve has an additional groove that connects ports 3 and 4 compared to the valve in its 'splitting and capture' mode as illustrated in FlG 3A.
  • port 4 also optionally connects to a split adjuster 50 to control the split ratio of the LC effluent.
  • the valve is in its 'infusion' mode.
  • the additional groove that connected ports 3 and 4 in FlG 3E rotates counterclockwise and now connects ports 2 and 3.
  • Port 3 also connects to an ancillary control device 90 to add the 'treating' flow to the captured portion of the LC effluent at the exit (i.e. port 2) of the tube 16.
  • Device 90 may be a stock solution connected to a pump which can control the flow rate of the solution adding to the captured portion.
  • port 4 can optionally connect to split adjuster 50 to control the flow rate of the captured portion entering a mass spectrometer.
  • the flow rate can be controlled by a feedback loop including a flow sensor and a split adjuster or a flow controller.
  • a flow rate sensor 80 which is connected to a control unitl OO monitors the flow rate in the tube 16 and sends the information to a split adjuster 50. The split adjuster then adjusts the flow rate accordingly to reach a predetermined value.
  • LC/MS system 10 can include more other features or devices to further improve the performance of the system.
  • another LC column e.g., a nano-LC column
  • mass spectrometer 18 e.g., as in FIG. 3G
  • An additional LC column can also be placed, e.g., at the distal end of tube 16 before the second portion (i.e., the captured portion) of the effluent undergoes MS analysis so that over broadening of chromatographic peaks corresponding to individual analytes due to molecular diffusion in the tube can be counteracted or corrected, for instance.
  • splitting an LC (e.g., HPLC) effluent prior to a nanoESI analytical device and mass spectrometer enables the acquisition of MS data on all of the components or analytes in the sample, searching the component MS data against a database, then redirecting the portion captured in the capillary tube to the nanoESI/MS device and conducting the MS experiments (e.g., MS/MS) based on the database search results.
  • this disclosure would be useful to analyze a mixture of peptides formed from cnzymatically digesting a protein(s) using nanoLC/MS while simultaneously capturing the separated peptides into a tube.
  • the MS data acquired can be analyzed against a database to propose the most probable proteins. Then an intelligent MS experiment targeting peptides that should be present in the second portion of the same sample (i.e., the captured chromatogram in the tube) can be produced to increase the probability of correctly identifying the protcin(s), especially if the peptides have very low signal intensities in the initial round of MS.
  • analysis of intact proteins which is traditionally difficult for MS to acquire enough data to identify the protein during a single LC/MS experiment, can be achieved with improved accuracy and sensitivity by combining the LC experiment with infusion nanoESI/MS analysis of captured proteins in a rube which substantially remain separated corresponding to the chromatog ⁇ am.
  • the proteins coming out of the tube may correspond to broader peaks due to diffusion forces, which enables a second, longer MS experiment to be performed on the same injection of a sample.
  • the extended time can allow more signal averaging or multiple MS or MS/MS acquisitions than those using conventional techniques.
  • the diffusion of separated components or analytcs in the capture tube can be controlled by various means, such as tube inner diameter, tube length, time in the tube (controlled by length of the nanoLC experiment, for example), or by lowering the tube temperature or introducing barriers between two components to prevent remixing. More discussion follows.
  • the tube 16 is configured to capture and store a portion of the effluent of the column for a later round of analysis, e.g., with extended analysis time compared to that available for the initial MS scanning of portion 24.
  • the tube 16 is a capillary tube and its dimension (e.g., inner diameter) is chosen to define a desired range of diffusion of analytcs for a desired outcome.
  • the capillary dimensions can be chosen based on the chromatographic peak volume exiting the LC column coupled to the capillary. When using 300 nL/min flow rate from a nano-LC column, peaks that are 12 seconds wide correspond to peak volumes of 60 nL.
  • the capture and storing tube 60 nL corresponds to a length of about 30 mm of the tube.
  • the length of tube can therefore be predetermined to capture and store one or more analytc peaks.
  • the tube can be a fused silica tube with an inner diameter of about 50 ⁇ m and a length of around 600 cm.
  • the diameter of the tube is selected to be on the micrometer scale so that diffusion of the captured LC- separated analytes can be controlled, e.g., reducing the likelihood of remixing the separated compounds and losing chromatographic separation.
  • the techniques described in the present disclosure can take into account characteristics of molecular diffusion in fluids (e.g., eluents) captured in a tube.
  • Molecules e.g., peptides or proteins
  • Molecular diffusion e.g., in a capillary tube, can be predicted based on capillary diai ⁇ cter. size of molecule, bulk solution properties and temperature.
  • the volume of solution where molecules of a given analytc spread per unit length of a capillary is proportional to the square radius of the capillary. In other words, the spreading length of molecules in a solution of fixed volume is inversely proportional to the square radius of the capillary.
  • the smaller the surface area e.g. the square radius of the capillary
  • reducing or minimizing the change in the volume of a solution of analyte molecules in a tube caused by molecular diffusion and/or reducing the surface area at the boundaries of two analyte zones can be accomplished by use of a capillary with reduced diameter. The effect is to stretch a fixed volume along the length of a capillary.
  • the length of a 50 nL volume which is dependent on the capillary diameter can vary from about I mm to about 2500 mm with capillary diameter changing from 250 ⁇ m to 5 ⁇ m.
  • molecular diffusion in the tube can be controlled for example, by inserting gas bubbles into the capillary to segment the solution, as illustrated in FIG 4. Molecules in solution can diffuse to the bubble/liquid interface but not beyond it. Referring to FlG 4, gas segments or bubbles 221 placed between two liquid segments 220 of effluent portion 22 in the capture tube 16.
  • An electrolysis electrode 70 can be placed at the entrance of the tube 16 and programmed to clcctrolyzc the mobile phase to create gas bubbles in a predetermined pattern, for example, gas segments can be created at a defined intervals, e.g., every 5OnL of liquid segment, or gas segments can be created between the elution of two analytcs, e.g., right after the elution of a first analyte and before the elution of a second analyte.
  • a reader that could detect the bubbles could be used at the exit of tube 16 so that specific liquid segments captured in the tube could be quickly positioned for analysis, e.g., a targeted analysis.
  • diffusion can be reduced by cooling the solution to a temperature below the room temperature, e.g., about 4°C.
  • controlled diffusion e.g., enhanced diffusion
  • Different embodiments might be combined to achieve the best control of diffusion based on specific requirement of the experiments.
  • a tube to store a portion of the LC effluent include keeping the analyte molecules in a solution, e.g., to prevent decomposition of the analyte upon drying or to prevent loss of precious sample by drying and rcdissolving it in a solvent.
  • temperature can be increased.
  • the system can capture intact protein separation, heat and digest proteins with the stored mobile phase.
  • Mass spectrometer or MS device 18 can be used for tandem MS, e.g., an infusion nanoESI/MS device.
  • the nanoESI sprayer or emitter can be a fused silica capillary with a pulled tip which has an i.d. of about 1 -15 ⁇ m, or an ESI Chip® available from Advion Biosciences, Inc., which is a microfluidics chip containing an array of nanoelectrospray nozzles, each one-fifth the diameter of a human hair, etched in a silicon wafer for nanoolceti ⁇ spruy.
  • One exemplary advantage is that storing a portion of a sample allows subsequent MS experiments to be adjusted to focus on analysis of components or analytcs of the sample missed by initial nanoLC/MS experiments.
  • previously identified components of the sample can be excluded from the data dependent acquisition during the subsequent infusion experiment (from the portion stored in the lube), therefore, infusion experiments are able to acquire MS/MS data on the lower-intensity components missed during the initial nanoLC/MS/MS experiment.
  • previously identified components of the sample can be included in data dependent acquisition (and others excluded) during the subsequent infusion experiment to further analyze those components in more detail.
  • the ancillary control device 90 in FIG 3C can be a pressurized vessel or a pump to introduec gas segments or non-mixing liquid segments into the eaptured portion to provide diffusion barriers and limit diffusion of analytcs.
  • the gas and non- mixing liquid arc immiscible with the mobile phase of the LC effluent.
  • the split ratio of the LC effluent can be fixed or varied during the division process, e.g., according to the different abundances of analytes, by adjusting the backpressure of the output ports. For example, if analytc A is 10 times as much as analyte B in the sample, when they are separated in the LC column, split ratio of effluent with analyte A may be set to 1 : 10 while split ratio of effluent with analyte B may be set to 1 : 1.
  • LC effluent directed to the capture capillary could be segmented and fraction collected into individual tubes (e.g., capillaries) with a tapered end on which a nanoESl sprayer could be formed.
  • each of N capillary tube can be connected to a port of a 1 :N splitter.
  • LC effluent can be divided to more than two portions and at least two portions are captured and stored in individual tubes (e.g., capillaries).
  • the splitter 14 can be a ten-port valve. Arrows in these figures indicate flow directions of the analytes.
  • the valve In its 'splitting and capture' mode, as illustrated in FlG 5A, the valve first splits the LC effluent from column 12 to two flows at port 10 with a first flow to port 1 then the mass spectrometer 18 and a second flow to port 9 which splits the flow again so that one portion of the second ilow is captured in tube 16A while the other portion of the second flow is directed to port 8 and captured in tube 16B.
  • the split adjuster 50 controls the split ratio of the first and second flow.
  • the captured portions in tubes 16A and 16B are driven to pass out of the tubes for analysis by the mobile phase of the column 12 connected to the pump 40.
  • the splitter 14 can be a valve assembly that includes a ten-port valve 14A and a six-port valve 14B connected by two capture tubes 16A and 16B, as illustrated in FIGS. 6A-6C. Arrows in these figures indicate flow directions of the analytes.
  • this valve assembly configuration enables individual controls over the flow rates of the individual captured portions thus enables control over both the split ratio of the initial LC effluent and the split ratio of the primary captured portion that is further split into at least two subsidiary captured portions.
  • the ten-port valve 14A first splits the LC effluent from column 12 to two flows at port 10 with a first flow to port 1 then the mass spectrometer 18 and a second flow to port 9 which splits the flow again so that one portion of the second flow is captured in tube 16A while the other portion of the second flow is directed to port 8 and captured in tube 16B.
  • Two split adjusters 50a and 50b that are in fluid communication with individual captured portions control the backpressures thus the flow rates in the capture tubes.
  • the flow rate ratio of captured portions in tube 16A and 16B can be selected by controlling split adjusters 50a and 50b with respect to each other while the split ratio of the LC effluent (split to first and second flows) can be adjusted by controlling cither or both of two split adjusters.
  • the captured portion in tube 16A or the portion in tube 16B may be redirected to a mass spectrometer for analysis while the other captured portion can be kept in the tube for later analysis.
  • one portion of the effluent of a nanoLC column is driven to the mass spectrometer while another portion is captured by a capillary tube.
  • the effluent passes from the autosamplcr 30 into the LC column 12 and into the splitter 14.
  • a first portion of the effluent passes into a second, smaller ID column 70 and then passes through a coupling device 80a that connects to a nanospray chip I I O with multiple channels.
  • a second portion of the effluent progresses from the splitter 14 through a capture capillary 80b.
  • the capture capillary 80b consists of a long capillary with a second chip coupling device at its end, which can be coupled to the chip 1 10 (but is not coupled in FIG 7A). After the nanoLC run has ended, the capture capillary 80b couples to the channel of the micro chip 110 through the coupling mechanism.
  • the effluent can be directed into column 70 or into capillary tube 80b by controlling the back pressures of the output ports of the splitter.
  • Factors that influence back pressure include the inner diameters and the lengths of the output ports as well as the tubes connected to them.
  • the inner diameters of the output ports and/or the tubes connected to them can be about 5 microns to 750 microns, e.g., 10 to 500 microns, 20 to 200 microns, or 50 to 100 microns.
  • the port leading to column 70 can have an i.d. of 15 microns and 15 centimeters of total tubing length while the capillary 80b can have an i.d.
  • Back pressure can also be affected by applying an external pressure to the split portions via, e.g., a spit adjustor.
  • the second portion passes from splitter 14 through capillary 80c and into the 6 port valve 60, where it flows through two connected channels (e.g., channels 1 and 6) into the capillary 80b.
  • the flow of the second portion can be controlled by using a pressure bomb 120 that is connected, e.g., to channel 5.
  • the pressure bomb 120 is a chamber that can be equipped with a small gas cylinder, a high pressure gauge, and a thick-walled metal chamber.
  • the pressure bomb can drive the captured portion of LC effluent to the MS device 18.
  • the flow rate can also depend on the tubing i.d. and length.
  • valve 60 switches to a second mode that connects the two ports with the pressure bomb 120 and the capture capillary.
  • the capture capillary 80b couples to the channel of the micro chip 110 through the coupling mechanism.

Abstract

A liquid chromatography/mass spectrometry system includes a chromatographic column (12) through which an effluent passes, wherein the effluent comprises a plurality of analytes that correspond to a plurality of chromatographic peaks and an eluent; a post-column splitter (14) having at least two output ports through which the effluent of the column is split to at least a first portion and a second portion; a mass spectrometer configured to receive the first portion from a first of the output ports for analysis; and a tube (10) connected to a second of the output ports configured to prevent substantial evaporation of the eluent in the second portion until undergoing mass spectrometry. The second portion has a plurality of separated analytes corresponding to at least two chromatographic peaks. A method of using the system is also disclosed.

Description

LIQUID CHROMATOGRAPHY-MASS SPECTROMETRY
TECHNICAL FIELD
This description relates to method and system for liquid chromatography-mass spectrometry (LC/MS) analyses of biological analytes such as proteins and/or peptides, and more particularly to data dependent nano-LC/MS acquisitions.
BACKGROUND
Liquid chromatography (LC) is a well-established analytical technique for separating components of a fluidic mixture for subsequent analysis and/or identification, in which a column, micro fluidic chip-based channel, or tube is packed with a stationary phase material that typically is a finely divided solid or gel such as small particles with diameter of a few microns. 'Hie small particle size provides a large surface area that can be modified with various chemistries creating a stationary phase. A liquid elucnt is pumped through the liquid chromatographic column ("LC column") at a desired flow rate based on the column dimensions and particle size. This liquid elucnt is sometimes referred to as the mobile phase. The sample to be analyzed is introduced (e.g., injected) in a small volume into the stream of the mobile phase prior to the LC column. The analytes in the sample are retarded by specific chemical and/or physical interactions with the stationary phase as they traverse the length of the column. The amount of retardation depends on the nature of the analytc, stationary phase and mobile phase composition. The time at which a specific analyte elutes or comes out of the end of the column is called the retention time or elution time and can be a reasonably identifying characteristic of a given analytc especially when combined with other analyzing characteristics such as the accurate mass of a given analyte. Or in other words, the analytes interact with the stationary phase based on the partition coefficients for each of the analytes. The partition coefficient is defined as the ratio of the time an analyte spends interacting with the stationary phase to the time spent interacting with the mobile phase. The longer an analyte interacts with the stationary phase, the higher the partition coefficient and the longer the analytc is retained on the LC column. An isocratic flow in LC describes a mobile phase of a constant composition. In contrast to this is the so called "gradient clution", which is a separation where the mobile phase composition changes during a separation process. For example, a 20-minutc gradient starts from 10% MeOH and ends up with 30% McOH within 20 minutes. Detection of analytcs separated on an LC or nanoLC column can be accomplished by use of a variety of different detectors. Spectroscopic detectors rely on a change in refractive index, ultraviolet and/or visible light absorption, or fluorescence after excitation with a suitable wavelength to detect the separated components. Additionally, the separated components may be passed from the liquid chromatographic column into other types of analytical instruments for further analysis, e.g., liquid chromatography-mass spectrometry (LC/MS or LC-MS) separates compounds chromatographically before they arc introduced to the ion source of a mass spectrometer.
The purpose of the LC column is to separate analytes such that a unique response (e.g., a UV absorption peak) for each analyte from a chosen detector can be acquired for a quantitative or qualitative measurement. The ability of a LC column to generate a separation is determined by the dimensions of the column and the particle size supporting the stationary phase. The retention time of an analyte can be adjusted by varying the mobile phase composition and the partition coefficient for an analyte. Increases in chromatographic separation can be achieved via a reduction in the LC column diameter, increasing LC column length and/or a reduction of stationary phase particle dimensions.
Mass spectrometry ("MS" or "mass-spec") is an analytical technique used to measure the mass-to-charge ratio of gas phase ions. This is achieved by ionizing the sample and separating ions of differing masses and recording their relative abundance by measuring intensities of ion flux. A typical mass spectrometer comprises three parts: an ion source, a mass analyzer, and a detector system. The ion source is the part of the mass spectrometer that ionizes the substance under analysis (the analyte). The ions arc then transported by magnetic or electric fields to the mass analyzer that separates the ions according to their mass-to-charge ratio (m/∑). Many mass spectrometers use two or more mass analyzers for tandem mass spectrometry (MS/MS). The detector records the charge induced or current produced when an ion passes by or hits a surface. A mass spectrum is the result of measuring the signal produced in the detector when scanning m/z ions with a mass analyzer. Mass spectrometry has rapidly developed as an important emerging method for the characterization of proteins. The two primary methods for ionization of whole proteins arc elcctrospray ionization (ESl) and matrix-assisted laser desorption/ionization (MALDI). In keeping with the performance and mass range of available mass spectrometers, two approaches are used for characterizing proteins. In the first, intact proteins are ionized by either of the two techniques described above, and then introduced to a mass analyzer. In the second, proteins arc cnzymatically digested into smaller peptides using an agent such as trypsin or pepsin. The collection of peptide products are then introduced to the mass analyzer. The latter is often referred to as the "bottom-up" approach of protein analysis. Proteins and/or peptides υf interest to biological researchers are usually part of a very complex mixture of other proteins and molecules that co-exist in the biological medium. The high complexity of biological mixtures often makes coupling a separation technique, such as high performance liquid chromatography (HPLC), highly desirable or even required after enzymatic digestion. In addition, HPLC on-line connected to ESI-MS offers the possibility for pre-conccntration of dilute samples, desalting and removal of detergents. In many applications, and especially where relatively small volumes of sample arc under analysis, improving detection sensitivity can become especially important. Improvement of detection sensitivity using concentration sensitive detectors such as UV/Vis absorbance and ESI mass spectrometers can be achieved by employing HPLC columns with smaller internal diameters (i.d.). For example, increased sensitivity during peptide analysis can result from using nano-LC (e.g., column i.d. of 50-100 μm) and capillary LC (e.g., column i.d. of 320 μm). Flow rate of the mobile phase through such columns is from several nanoliters per minute (nL/min), to several microliters per minute (μL/min), and the mobile phase can be sprayed directly without post- column splitting. The process of elcctrospray ionization at flow rates on the order of nanoliters ("nL") per minute has been referred to as "nanoclectrospray ionization" (nanoESI).
Elcctrospray ionization (ESI) or nanoESI is a commonly applied ionization technique when dealing with biomolccules such as peptides and proteins. The electrospray process creates highly-charged droplets that, under evaporation, create ions representative of the species contained in the solution. An ion-sampling orifice of a mass spectrometer may be used to sample these gas phase ions for mass analysis. When an electric potential or field is applied to the outlet of a conducting needle (often referred to as a sprayer or emitter) relative to an extracting electrode, such as one provided at the ion-sampling orifice of a mass spectrometer, the electric field generated on the needle causes the separation of positively and negatively charged ions in solution and pushes ions of one polarity (e.g., positively charged or negatively charged) to the solution surface. The higher the electric field is the greater the surface charge repulsion force that counteracts the fluid surface tension is. When the repulsion force of the solvated ions exceeds the surface tension of the fluid being electrosprayed, a volume of the fluid is pulled into the shape of a cone, known as a Taylor cone, which extends from the tip of the needle. A liquid jet extends from the tip of the Taylor cone and becomes unstable and generates charged-droplcts. These small charged droplets are drawn toward the extracting electrode, e.g., the sampling electrode of a mass spectrometer. The small droplets are highly- charged and solvent evaporation from the droplets results in the excess charge in the droplet residing on the analyte molecules in the electrosprayed fluid. The charged molecules or ions are drawn through the ion-sampling orifice of the mass spectrometer for mass analysis. The potential voltage ("V") required to initiate an elcctrospray is dependent on the size of the sprayer, the surface tension of the solution, and the electric field can be on the order of approximately I O6 V/m. The physical si/.e of the needle and the fluid surface tension determines the density of electric field lines necessary to initiate electrospray.
In so-called nanoelectrospray, the sample is sprayed from a needle with a tip diameter less than about 5 μm, using a sample flow rate between 5 nL/min and 50 nL/min, for example. Charged droplets with diameters less than 1 micron can be formed at flow rates less than 40 nL/min. These small, highly-charged droplets can provide more efficient ionization of analytes contained within the droplets due to higher surface-to-volumc ratios and smaller radii through which analytes need to diffuse to reach the charged surface of the droplets compared to conventional ESl. NanoESl-MS can thus be used for analyzing small amounts of sample with low sample concentrations (e.g., fcmtomolc/microlitcr). Moreover, with nanoESI, the ion response for analytes contained in a sample solution is proportional to its concentration instead of its total amount. What this means is that if a solution is being sprayed at 200 nL/min or 50 nL/min or 20 nL/min the signal intensity as measured using mass spectrometry would be the same. Thus reducing a flow rate by a factor of 5 roughly increases mass spectrometry scans to be acquired for the same amount of sample by a factor of 5. As a result, signal averaging from the increased number of scans improves signal-to-noisc ratios and ion statistics which enable multiple MS/MS experiments on the analytes and high accuracy in identifying analytcs.
Tandem mass spectrometry (MS/MS) is a popular experimental method for identifying biomolecules such as proteins. Tandem MS involves multiple steps of mass selection or analysis, usually separated by some form of fragmentation. A tandem mass spectrometer is capable of multiple stages of mass spectrometry. For example, one mass analyzer can isolate one peptide from many others entering a mass spectrometer. A second mass analyzer then stabilizes the peptide ions while they collide with a gas, causing them to fragment by collision- induced dissociation (CID). A third mass analyzer then characterizes the fragments produced from the peptides. Tandem MS can also be done in a single mass analyzer over time as in a quadrupυle iυn trap. There arc various methods for fragmenting molecules for tandem MS, including collision-induced dissociation (CID), electron capture dissociation (ECD), electron transfer dissociation (ETD), infrared multiphoton dissociation (IRMPD) and blackbody infrared radiative dissociation (BIRD). Characterization of total digests (peptides) of complex protein mixtures using
HPLC/MS is also called shotgun proteomics. Shotgun analysis involves direct digestion of protein mixtures to complex peptide mixtures, followed by the automated identification of the peptides by liquid chromatography combined with tandem mass spectrometry (LC-MS/MS). The development of shotgun proteomics today couples nano-LC for peptide analysis, automated MS to MS/MS data acquisition software and hardware on modern tandem mass spectrometers, along with data searching software of modern search engines. Modern mass spectrometers with data dependent scanning software are capable of acquiring MS and MS/MS data from many hundreds of peptides per hour.
The principle of shotgun analysis is to first "spread out" peptides in complex mixtures by multidimensional chromatographic separation. Tandem MS instruments then acquire peptide MS/MS spectra, which encode the peptide sequences. This acquisition can be done in a data-dependent way, whereby the instrument relics on a preliminary scan, performed as the peptides enter the instrument, to select peptides for fragmentation and generation of MS/MS spectra. SUMMARY
In one aspect, in general, a liquid chromatography system includes: a chromatographic column through which an effluent passes, wherein the effluent comprises a plurality of analytcs that correspond to a plurality of chromatographic peaks and an eluent; a post-column splitter having at least two output ports through which the effluent of the column is split to at least a first portion and a second portion; a mass spectrometer configured to receive the first portion from a first of the output ports for analysis; and a tube connected to a second of the output ports configured to prevent substantial evaporation of the eluent in the second portion until undergoing mass spectrometry. The second portion has a plurality of separated analytes corresponding to at least two chromatographic peaks.
Aspects can include one or more of the following features.
The system is configured to direct the second portion to the mass spectrometer after the first portion is analyzed by the mass spectrometer.
The system further comprises a pump connected to the tube to pump the second portion to the mass spectrometer after the first portion is analyzed by the mass spectrometer.
Hie system further comprises a second detector configured to receive the second portion irom the tube after the first portion is analysed by the mass spectrometer.
The second detector comprises a mass spectrometer.
The second detector comprises an infusion nanoESI/MS device. The tube is configured to substantially reduce the diffusion of the analytes in the effluent stored in the tube.
The tube is configured to stay at a temperature lower than the room temperature.
The tube comprises an electrolysis electrode to elcctrolyze the eluent to produce a gas segment between any two eluent segments. The electrolysis is triggered by an analytical device.
The device is an ultraviolet detector, fluorescence detector, an electrochemical detector, evaporative light scattering detector, nuclear magnetic resonant spectrometer, charged aerosol detector, refractive index detector, or a mass spectrometer.
The mass spectrometer comprises an clectrospray sprayer. The mass spectrometer comprises an ESI/MS device.
The mass spectrometer comprises an infusion nanoESI/MS device. The infusion nanoESI/MS device comprises a nanoESI sprayer.
The nanoESI sprayer comprises a pulled tip of a fused silica capillary.
The infusion nanoESI/MS device comprises a chip containing an array of nanoclcctrospray nozzles. The tube comprises a fused silica capillary.
The tube has a diameter of 250 μm or less.
The tube has a diameter of 100 μm or less.
The tube has a diameter of 75 μm or less.
The tube has a diameter of 50 μm or less. The tube has a length of about 1 meter or more.
The tube has a length of about 10 meters or less.
The tube has a length of about 6 meters.
The second portion is directed for mass spectrometry at a lower flow rate than the first portion is. The splitter comprises a T-shape piece that creates a volume ratio of about 4: 1 to about
1 : 1 of the second portion to the first potion.
The splitter comprises a valve that has at least five ports, a first connector connecting two of said ports, and a second connector connecting three or more of the rest said ports to split the effluent. The valve has at least six ports.
The valve has at least one port connected to a flow controller.
The valve has two ports that arc connected by the tube.
The valve is switchable between at least two configurations, including a first configuration in which the second connector connects a first set of three ports, and a second configuration in which the second connector connects a second set of ports different from the first set.
ITic analytes in the second portion exit the tube in the same order in which the analytcs exit the chromatographic column.
The analytes in the second portion exit the tube in a reversed order in which the analytes exit the chromatographic column. The second portion is mixed with a stream of liquid before the portion undergoes mass spectrometry.
The second portion has a plurality of separated analytes corresponding to at least half of the plurality of chromatographic peaks corresponding to the analytes that pass through the chromatographic column.
The second portion has a plurality of separated analytes corresponding to at least 90% of the plurality of chromatographic peaks corresponding to the analytes that pass through the chromatographic column.
The system further comprises a second chromatographic column, wherein the inner diameter of the second column is smaller than that of the first column.
In another aspect, in general, a method of characterizing an analyte in a sample includes: passing an effluent comprising a plurality of analytes and an eluent through a chromatographic column, the analytes corresponding to a plurality of chromatographic peaks; splitting at least a first portion and a second portion of the effluent from respective output ports of a post-column splitter, the first portion being directed from a first of the output ports to a mass spectrometer for analysis; and receiving the second portion having a plurality of separated analytes corresponding to at least two chromatographic peaks in a tube connected to a second of the output ports to prevent substantial evaporation of the eluent before undergoing mass spectrometry. The method further comprises directing the second portion irom the tube to the mass spectrometer after the first portion is analyzed by the mass spectrometer.
The method further comprises directing the second portion from the tube to a second mass spectrometer after the first portion is analyzed by the mass spectrometer.
The method further comprises analyzing a first analyte from the stored second portion after a second analyte from the first portion has been analyzed by the mass spectrometer, wherein the first analyte passed out of the chromatographic column before the second analyte passed out of the chromatographic column.
The method further comprises analyzing a first analyte from the stored second portion after a second analyte from the second stored portion has been analyzed by the mass spectrometer, wherein the first analyte passed out of the chromatographic column before the second analyte passed out of the chromatographic column. The method further comprises analyzing a first analyte from the stored second portion before a second analyte from the second stored portion has been analyzed by the mass spectrometer, wherein the first analyte passed out of the chromatographic column before the second analyte passed out of the chromatographic column. The method further comprises cooling the second portion to substantially reduce diffusion of the analytcs in the elucnt captured in the tube.
The method further comprises segmenting the stored second portion into a least two segments in the tube by a gas bubble wherein the gas bubble creates a diffusion boundary to the analytcs in the portion. The gas bubble is formed by electrolysis of the eluent of the second portion.
The method further comprises recording the segment positions in the tube by counting gas bubbles.
The method further comprises segmenting the stored second portion into at least two segments in the tube by a non-mixing liquid segment wherein the non-mixing liquid segment creates a diffusion boundary to the analytes in the portion.
The method further comprises directing the stored second portion in the rube to the mass spectrometer at a calibrated ilow rate controlled by a pump connected to the tube.
The calibrated flow rate is less than 5,000 nL/min.
The calibrated flow rate is less than 1 ,000 nL/min. The calibrated flow rate is less than 200 nL/min.
The second portion has a plurality of separated analytcs corresponding to at least half of the plurality of chromatographic peaks corresponding to the analytes that pass through the chromatographic column.
The second portion has a plurality of separated analytcs corresponding to at least 90% of the plurality of chromatographic peaks corresponding to the analytes that pass through the chromatographic column.
The method further comprises directing the effluent into a second chromatographic column.
The directing is performed by controlling back pressures of the splitter by connecting a pump to a port of the splitter.
Aspects may include one or more of the following advantages. A post-column splitter can divide a liquid chromatographic effluent such that a first fraction of the effluent is subjected to immediate nanoclectrospray mass spectrometry analysis while a second fraction is captured and stored in a tube, e.g., a capillary tube with i.d. of about a few tens of microns. The splitter can be a T-shapc piece, or chip-based channels, or a multi- port valve that can divide the effluent. The splitter can also be configured to divide the effluent to more than two fractions thus allow more than one fractions to be captured and stored in individual tubes for later usage. The dimension of the capture tube is selected to control diffusion of analytcs molecules so that the degree of remixing of the separated analytcs can be controlled or minimized. Gas segments can be introduced to the captured fraction to further limit diffusion of LC-separated analytes to confined regions and thus greatly increase storing time of the faction. Moreover, using a tube to store a fraction of the LC effluent allows the analytc molecules maintained in a solution, e.g., to prevent decomposition of the analyte upon drying or to prevent loss of precious sample by drying and redissolving it in a solvent. The second fraction collected in the tube can be redirected to a nanoESl sprayer to enable additional MS data to be acquired from the same sample injection based on the initial MS analysis of the first fraction, e.g., at a lower flow rate to the sprayer for targeted analytes or skipping analysis oiTcss interesting analytcs in the fraction to save time. The captured fraction can also be modified or treated before MS analysis by, e.g., adding another solvent, or undergoing another LC analysis, e.g., ion exchange chromatography. The details of one or more embodiments of the invention are set forth in the accompanying drawings and the description below. Other features, objects, and advantages of the invention will be apparent from the description and drawings, and from the claims.
DESCRI PTION OF DRAWINGS
FIG I A is a simplified cross-sectional schematic of a LC/MS system. FIG. I B is a cross-sectional schematic of an embodiment.
FIGS. 2 A and 2B are schematics of a LC/MS system. FIGS. 3A-G arc schematics of another embodiment. FIG. 4 is a cross-sectional view of an embodiment of a capture tube. FIGS. 5 A and 5B are schematics of still another embodiment. FIGS. 6A-C arc schematics of yet another embodiment.
FIGS. 7A-C arc schematics of embodiments with a capture capillary. DETAILED DESCRIPTION
Liquid chromatography (LC) with columns of small internal diameters, e.g., capillary LC and nano-LC columns, can be coupled with nanoESI to combine the benefits of sample separation and/or concentration in columns of small diameters and improved ionization efficiencies with nanoESl. For good LC separation resolution, peak widths should be narrow, but narrow peaks limit the acquisition time for mass spectral data. Preferably, an analytical system should enable separation of all compounds within an HPLC system (narrow peaks and high peak capacity), while enabling essentially unlimited time to acquire mass spectrometric data for each separated compound. For example, peak width at half height of compounds cluting from capillary- or nano-LC columns is generally in the range of 5 seconds to 30 seconds. During this period, the peptide needs to be sequenccd, which may require multiple stages of MS detection. Sequencing of the peptides is performed by compaπng measured and calculated fragment spectra. These scan cycles take approximately a few hundred milliseconds to a few seconds, which allows the experiment to perform only limited numbers of cycles during the clution of a chromatographic peak.
Some nano-LC/nanoESI-MS techniques spray the entire effluent exiting the nano-LC column with a nanoESI sprayer. As discussed above, each analytc cluting from a column occurs as a transient with a time profile of seconds. When samples become complex and contain multiple analytcs that are co-eluting, data-dependent scanning or other methods of MS/MS such as ECD or ETD may not be able to acquire spectra fast enough to identify all the analytes, e.g., peptides, as they enter the MS instrument, thus many analyte identifications can be missed. Often times it is only possible to collect MS/MS data on components of highest intensities in the initial MS scanning, thus restricting dynamic range for component identification. The present disclosure includes description of techniques that are able to solve these problems. For example, the strengths of nano liquid chromatography/mass spectrometry (nanoLC/MS) and infusion nanoelectrospray mass spectrometry (nanoESI/MS) can be combined with a post-column splitter that divides die LC effluent such that a first portion or fraction of the effluent is subjected to nanoelectrospray mass spectrometry analysis immediately after chromatographic separation and a second portion or fraction is captured and stored in a tube, e.g., a capillary tube with i.d. of about 20 - 50 μm. After a short time, e.g., following completion of the LC separation of the entire or partial sample injection, and/or completion of an initial MS analysis of the first portion of the effluent, the second portion collected in the tube can be redirected to a nanoESl sprayer to enable additional MS data to be acquired from the same sample injection based on the initial MS analysis to allow more signal averaging and improve accuracy of sample identification or protcome coverage in a shotgun experiment, for instance.
Referring to FlG 1 A, an LC/MS system 10 includes a liquid chromatographic column 12, e.g., a nano-LC column, which provides on-line separation capabilities to mass spectral analysis of the effluent 20 containing a plurality of separated analytes (illustrated as squares, circles, crosses, and triangles). A portion 24 of the effluent 20 is directed via some tubing 19 (e.g., a capillary tube) to mass spectrometer or MS device 18, e.g., a nanoESI/MS device. Another portion 22 of the effluent 20 is simultaneously captured and stored in a tube 16 which is configured to control (e.g., to reduce) the diffusion of the analytes in the effluent inside the tube 16 and substantially preserve the chromatographic separation of analytes from the column 12. 'ITic effluent 20 is split by a post-column splitter 14 to at least two portions 22 and 24.
While the portion 24 is undergoing mass spectral analysis in the MS device 1 8, the portion 22 of the effluent can, in some cases, keep entering tube 16 and keep moving along in tube 16. Or1 in other cases in which it may be desirable to store the portion 22 for longer periods of time, the portion 22 can be kept substantially stationary in tube 16 for a period of time that is long enough for the MS device 18 to further analyze the portion 24. Usually after the scanning of the portion 24 has been completed, the portion 22 can be redirected through the tube 16 and the splitter 14 to the MS device 18 (or redirected to a different MS device) for a second round of analysis, e.g., tandem MS. In some embodiments, tubing 19, splitter 14, and/or the tube 16 and can be integrated into a microfluidic chip, e.g., a chip containing a splitter connected to a long channel (e.g., a microfluidic channel) functioning as tubing 19 and/or tube 16.
In some embodiments, column 12 can be an HPLC column with an internal diameter in the micrometer scale, e.g., a nano-LC column of 75 μm i.d., and the flow rate can be controlled by a nano-LC pump to range between about 10 nL/min to 1000 nL/min, e.g., about 200 nL/min to 300 nL/inin. The post-column splitter 14 can be a T-shape piece ("Tee") as shown in FlG 1 B.
Referring particularly to FlG 1 B, the T-shape piece includes an input port 1 1 which can be connected to an outlet of the nano-LC column, two output ports 13 and 15 which divides the LC effluent 20 entering the Tee into two portions (shown as portion 24 to MS device and portion 22 to capture tube), and an air tight fitting 17 which holds the three ports together and allows fluid communication between the ports. Each of the two output ports can be an integral part of the tubing or tube that the two split portions enter respectively, e.g., port 13 can be the proximal end of tubing 19 (in FlG I A) and port 15 can be the proximal end of tube 16 (in FIG IA) with respect to the flow direction. The split ratio, usually the flow rate ratio of the two portions 24 and 22, e.g., portion to be analyzed vs. portion to be stored, can be adjustable from 1 : 100 to 10: 1 , e.g., from 1 : 10 to 5: 1 , from 1 :3 to 4: 1 , from 1 : 1 to 3: 1 , according to different experimental needs. For example, if flow rate of portion 24 is required to be 50-100 nL/min, when the flow rate of the LC effluent is 200 nL/min, the flow rate ratio would be selected to be 1 :3 to 1 : 1.
The flow rate ratio can be adjusted by controlling the back pressures of the output ports of the splitter. There are several factors that influence back pressure, such as the inner diameters and lengths of the output ports and tubes connected to them. In some embodiments, the inner diameters of the output ports and/or the tubes connected to them can be about 5 μm to 750 μm, e.g., 10 to 500 μm, 20 to 200 μm, or 50 to 100 μm. For example, in a particular embodiment, port 13 can have 15 μm i.d. with 15 centimeters of total tubing length while port 15 has 50 μm i.d. with 600 cm of total tube length to achieve a flow rate ratio of 1 :3. Back pressure can also be affected by applying external pressure to the split portions via, e.g., a spit adjustor, more detail of which follows.
Referring particularly to FIGS. 2A and 2B, an LC/MS system 10 can further include an autosamplcr 30 upstream of the LC column 12. The mobile phase or the eluent for LC is driven by a pump 40 which can also adjust the flow rate of mobile phase on the order of nL/min. The arrows in FIGS. 2A and 2B indicate flow directions of the mobile phase. The system 10 can switch between a first "online LC/MS plus splitting" mode (FlG 2A) and a second "no- splitting infusion" mode (FlG 2B) via use of a multiple port valve, e.g., a micro switching valve 60 having six ports labeled 1 through 6 with every port conncctable to either one of the two neighboring ports through a connector such as a groove or channel (not shown but connection is illustrated by arrows or lines between each two ports) in the valve. For example, for system 10 to be in the first mode as shown in FlG. 2A, ports 5 and 6 of valve 60 arc in fluid communication so that the pump 40 can drive the mobile phase to carry the sample from the autosampler through the LC column 12 then through post-column splitter 14. As discussed above, a first portion of the effluent of column 12 is directly driven to the mass spectrometer 18 while a second portion is captured by a tube 16. A device 50 is connected to port 3 of the valve 60. In some cases, the device 50 can be a waste or a split adjustor for, e.g., controlling the flow rate of the captured portion in tube 16. In other cases, the device 50 can be a second mass spectrometer, e.g., a nanoESI/MS device to analyze the captured portion based on the analysis results from the first portion. For system I O to be in the second mode as shown in FlG 2B, ports 5 and 4 of valve 60 arc in fluid communication so that the pump 40 can drive the captured portion of LC effluent back to the splitter 14 then to MS device 18 where the order of analytcs in the captured portion entering the MS device is reversed due to this set up configuration, i.e., the first into the tube will be the last out for MS analysis. In this mode, since port 1 is blocked with a plug or the like, the back pressure of column 12 can prevent the captured portion flowing back to the LC column. In some embodiments, a closing valve might be used between column 12 and splitter 14 to prevent the back flow to column 12. The selection between the two modes can either be manually or automatically controlled. The timing of switching from one mode to another can be experiment specific. For example, one can switch system 10 from the first mode to the second only after all components of the sample has been LC separated and elutcd; or one can do so intermittently by pausing the LC separation when it is necessary. In some embodiments, the captured effluent portion may be directed to another analytical device or another mass spectrometer, e.g., another nanoESI/MS.
In other embodiments, splitter 14 can be a multiple-port micro switching valve with at least one groove or channel that connects three or more ports simultaneously so that the valve can not only exhibit the same function as a T-shape splitter but also have additional functional features. As an example, a 6-port valve is shown in FIGS. 3A through 3F. Arrows in these figures indicate flow directions of the analytes. Referring particularly to FIG 3 A, valve 14 is in the 'splitting and capture' mode, and unlike in a conventional switching valve, port 6 is connected to both of its two neighboring ports (ports 1 and 5) through a groove or channel of the valve as well as connected to an outlet of the LC column 12 simultaneously so that the effluent from column 12 can be split into two portions with one flowing to the MS device 18 while the other flowing into a capture tube 16 connecting ports 5 and 2. Ports 2 and 3 are connected through another groove or channel of the valve in this mode. Port 3 is also connected to a split adjuster 50 to adjust the nanoLC split ratio, e.g., the flow rate ratio of port 1 to port 5, while port 4 is isolated from the other ports. The split adjuster can either be a pressurized vessel or a pump, which is used to adjust the back pressure of the tube 16 in order to control the split ratio, as discussed above. Referring particularly to FIG 3B, valve 14 is switched to the 'infusion' mode. The groove that connected port 6 to ports 1 and 5 in the 'splitting and capture' mode now rotates counterclockwise so that port 5 is connected to both of its neighboring ports (ports 4 and 6) simultaneously while the groove that connected ports 2 and 3 now connects ports 1 and 2. The resulting configuration is then port 6 connected to the pump 40 through column 12 and port 2 connected to port 1 so that the captured portion of separated analytes in tube 16 between ports 5 and 2 can be driven by the mobile phase of column 12 into the MS device 18 through port 1. The flow rate of the mobile phase is controlled by pump 40. Optionally, port 4 can connect to a split adjuster 50 to adjust the flow rate of the captured portion entering MS device 18 without having to decrease the flow rate of the mobile phase in LC column 12. For example, the flow rate in LC column can be kept at 200 nL/min while the flow rate in tube 16 can be adjusted to 50 nL/min by bifurcating the mobile phase exiting the LC column at port 5 with about three fourths of the mobile phase flowing to port 4 with the assistance of the split adjuster 50. In some embodiments, the captured effluent portion may be directed to another analytical device or another mass spectrometer, e.g., another nanoESI/MS. In some embodiments, in this 'infusion' mode, the flow for infusion nanoESI/MS of the captured chromatogram can be driven by the column wash in the column regeneration steps thereby enabling simultaneous infusion experiment and column preparation for the next injection which leads to an improvement in speed and efficiency of the analytical process, for example. In embodiments, the grooves in the valve connecting neighboring ports have a width of about 10-150 μm and a depth of about 5-75 μm. Compared to the set up configuration with a T-shape splitter discussed above, the valve structure of splitter 14 enables the order of the analytes in the captured portion entering the MS device to be the same order of exiting the LC column, i.e., the first into the capture tube will be the first out for MS analysis. One potential benefit of using this valve configuration is that the analytes or components captured into the tube each go in one end and out the other, thereby traversing the same length and arc subjected to a similar degree of diffusion so that the chromatographic peaks have similar degree of broadening.
In some embodiments, composition modification or treatment of the captured portion of the separated analytes in tube 16 may be desired, e.g., adding a different mobile phase to increase ionization of the analytes for mass spectrometry experiment. The modification of the captured portion may achieve, e.g., changes in ionization, electrochemical modification of captured components, enzyme degradation of intact proteins or peptides, mass tagging, or enzymatic de-phosphorylation of peptides or proteins, thus providing additional assistance in sample characterization. Two exemplary approaches of introducing a 'treating' flow of, e.g., a compound, a rcactant to a given analyte, a salt, and/or a mobile phase, to the captured portion in tube 16 are illustrated in FIGS. 3C-3D and 3E-3F, namely the 'prc-tubc' and 'post-tube1 approaches.
Referring particularly to FlG. 3C, with the 'pre-tube' approach, the 6-port switch valve has an additional groove that connects ports 4 and 5 compared to the valve in its 'splitting and capture' mode as illustrated in FlG 3A. Port 4 also connects to an ancillary control device 90 to add the 'treating' flow to the captured portion of the LC effluent at the entrance (i.e. port 5) of the tube 16. This approach may be selected when longer treatment time is desired. Device 90 may be a stock solution connected to a pump which can control the flow rate of the solution adding to the captured portion. As discussed above, the split adjuster 50 connected to port 3 can control the split ratio of the LC effluent. Referring to FIG 3D, the valve is in its 'infusion' mode. The additional groove that connected ports 4 and 5 in FIG 3C rotates counterclockwise and now connects ports 4 and 3. Similar to the embodiment in FIG 3B, in the 'infusion' mode, port 3 can optionally connect to split adjuster 50 to control the flow rate of the captured portion entering a mass spectrometer.
Referring particularly to FIG 3E, with the 'post-tube' approach, the 6-port switch valve has an additional groove that connects ports 3 and 4 compared to the valve in its 'splitting and capture' mode as illustrated in FlG 3A. As discussed above, port 4 also optionally connects to a split adjuster 50 to control the split ratio of the LC effluent. Referring to FIG 3F, the valve is in its 'infusion' mode. The additional groove that connected ports 3 and 4 in FlG 3E rotates counterclockwise and now connects ports 2 and 3. Port 3 also connects to an ancillary control device 90 to add the 'treating' flow to the captured portion of the LC effluent at the exit (i.e. port 2) of the tube 16. This approach may be selected when short treatment time is desired. Device 90 may be a stock solution connected to a pump which can control the flow rate of the solution adding to the captured portion. In the 'infusion' mode, port 4 can optionally connect to split adjuster 50 to control the flow rate of the captured portion entering a mass spectrometer. In embodiments, the flow rate can be controlled by a feedback loop including a flow sensor and a split adjuster or a flow controller. As shown is FIG 3G, a flow rate sensor 80 which is connected to a control unitl OO monitors the flow rate in the tube 16 and sends the information to a split adjuster 50. The split adjuster then adjusts the flow rate accordingly to reach a predetermined value.
In some embodiments, more other features or devices can be included in the LC/MS system 10 to further improve the performance of the system. For example, another LC column (e.g., a nano-LC column) can be placed, e.g., between port 1 and mass spectrometer 18 (e.g., as in FIG. 3G), to further separate and/or concentrate analytes of first portion of the LC effluent of column 12. An additional LC column can also be placed, e.g., at the distal end of tube 16 before the second portion (i.e., the captured portion) of the effluent undergoes MS analysis so that over broadening of chromatographic peaks corresponding to individual analytes due to molecular diffusion in the tube can be counteracted or corrected, for instance.
As discussed above, splitting an LC (e.g., HPLC) effluent prior to a nanoESI analytical device and mass spectrometer enables the acquisition of MS data on all of the components or analytes in the sample, searching the component MS data against a database, then redirecting the portion captured in the capillary tube to the nanoESI/MS device and conducting the MS experiments (e.g., MS/MS) based on the database search results. For example, this disclosure would be useful to analyze a mixture of peptides formed from cnzymatically digesting a protein(s) using nanoLC/MS while simultaneously capturing the separated peptides into a tube. At the end of the initial round of nanoLC/MS experiment on the first portion of the sample, the MS data acquired can be analyzed against a database to propose the most probable proteins. Then an intelligent MS experiment targeting peptides that should be present in the second portion of the same sample (i.e., the captured chromatogram in the tube) can be produced to increase the probability of correctly identifying the protcin(s), especially if the peptides have very low signal intensities in the initial round of MS. In another example, analysis of intact proteins, which is traditionally difficult for MS to acquire enough data to identify the protein during a single LC/MS experiment, can be achieved with improved accuracy and sensitivity by combining the LC experiment with infusion nanoESI/MS analysis of captured proteins in a rube which substantially remain separated corresponding to the chromatogτam. The proteins coming out of the tube may correspond to broader peaks due to diffusion forces, which enables a second, longer MS experiment to be performed on the same injection of a sample. The extended time can allow more signal averaging or multiple MS or MS/MS acquisitions than those using conventional techniques. The diffusion of separated components or analytcs in the capture tube can be controlled by various means, such as tube inner diameter, tube length, time in the tube (controlled by length of the nanoLC experiment, for example), or by lowering the tube temperature or introducing barriers between two components to prevent remixing. More discussion follows.
The tube 16 is configured to capture and store a portion of the effluent of the column for a later round of analysis, e.g., with extended analysis time compared to that available for the initial MS scanning of portion 24. In some embodiments, the tube 16 is a capillary tube and its dimension (e.g., inner diameter) is chosen to define a desired range of diffusion of analytcs for a desired outcome. For example, the capillary dimensions can be chosen based on the chromatographic peak volume exiting the LC column coupled to the capillary. When using 300 nL/min flow rate from a nano-LC column, peaks that are 12 seconds wide correspond to peak volumes of 60 nL. If a 50 micron inner diameter capillary tube is used as the capture and storing tube, 60 nL corresponds to a length of about 30 mm of the tube. The length of tube can therefore be predetermined to capture and store one or more analytc peaks. In a particular embodiment, the tube can be a fused silica tube with an inner diameter of about 50 μm and a length of around 600 cm. The diameter of the tube is selected to be on the micrometer scale so that diffusion of the captured LC- separated analytes can be controlled, e.g., reducing the likelihood of remixing the separated compounds and losing chromatographic separation.
The techniques described in the present disclosure can take into account characteristics of molecular diffusion in fluids (e.g., eluents) captured in a tube. Molecules (e.g., peptides or proteins) in solution can diffuse randomly in all directions. Molecular diffusion e.g., in a capillary tube, can be predicted based on capillary diaiπcter. size of molecule, bulk solution properties and temperature. The volume of solution where molecules of a given analytc spread per unit length of a capillary is proportional to the square radius of the capillary. In other words, the spreading length of molecules in a solution of fixed volume is inversely proportional to the square radius of the capillary. In addition, the smaller the surface area (e.g. the square radius of the capillary) is, the less frequently or less likely diffusion takes place. As a consequence, reducing or minimizing the change in the volume of a solution of analyte molecules in a tube caused by molecular diffusion and/or reducing the surface area at the boundaries of two analyte zones can be accomplished by use of a capillary with reduced diameter. The effect is to stretch a fixed volume along the length of a capillary. For example, a typical analyte separated by nano-LC at a flow rate of 200 nL/min exits the column in a volume of approximately 50 nL The length of a 50 nL volume which is dependent on the capillary diameter can vary from about I mm to about 2500 mm with capillary diameter changing from 250 μm to 5 μm.
In some embodiments, molecular diffusion in the tube can be controlled for example, by inserting gas bubbles into the capillary to segment the solution, as illustrated in FIG 4. Molecules in solution can diffuse to the bubble/liquid interface but not beyond it. Referring to FlG 4, gas segments or bubbles 221 placed between two liquid segments 220 of effluent portion 22 in the capture tube 16. An electrolysis electrode 70 can be placed at the entrance of the tube 16 and programmed to clcctrolyzc the mobile phase to create gas bubbles in a predetermined pattern, for example, gas segments can be created at a defined intervals, e.g., every 5OnL of liquid segment, or gas segments can be created between the elution of two analytcs, e.g., right after the elution of a first analyte and before the elution of a second analyte. Further discussion of generating gas segments is disclosed in Khan, ct al., "Microfluidic Synthesis of Colloidal Silica", Lanymuir, 20, 8604-8611 (2004), and Zheng, et al ., "A Microfluidic Approach for Screening Submicroliter Volumes against Multiple Reagents by Using Preformed Arrays of Nanolitcr Plugs in a Three-Phasc Liquid/Liquid/Gas Flow", Angcw. Chcm. Int. Ed., 44, 2520-2523 (2005), the entire contents of each of which are hereby incorporated by reference herein. In some embodiments, a reader (optical or thermal) that could detect the bubbles could be used at the exit of tube 16 so that specific liquid segments captured in the tube could be quickly positioned for analysis, e.g., a targeted analysis. In some embodiments, diffusion can be reduced by cooling the solution to a temperature below the room temperature, e.g., about 4°C. In yet some other embodiments, controlled diffusion (e.g., enhanced diffusion) may be beneficial when the sample is analyzed by infusion nanoESl/MS since the lime for acquiring analyte signals and for more MS analyzing cycles will be extended as the analyte diffuses to spread within higher volume which leads to longer time for the analyte to exit the tube at a fixed flow rate. Different embodiments might be combined to achieve the best control of diffusion based on specific requirement of the experiments.
Moreover, other potential benefits of using a tube to store a portion of the LC effluent include keeping the analyte molecules in a solution, e.g., to prevent decomposition of the analyte upon drying or to prevent loss of precious sample by drying and rcdissolving it in a solvent. In some embodiments, temperature can be increased. For example, the system can capture intact protein separation, heat and digest proteins with the stored mobile phase.
Mass spectrometer or MS device 18 can be used for tandem MS, e.g., an infusion nanoESI/MS device. The nanoESI sprayer or emitter can be a fused silica capillary with a pulled tip which has an i.d. of about 1 -15 μm, or an ESI Chip® available from Advion Biosciences, Inc., which is a microfluidics chip containing an array of nanoelectrospray nozzles, each one-fifth the diameter of a human hair, etched in a silicon wafer for nanoolcetiυspruy.
Many advantages of the techniques described in present disclosure including reserving or storing a portion of a sample have been apparent from the description of different embodiments. One exemplary advantage is that storing a portion of a sample allows subsequent MS experiments to be adjusted to focus on analysis of components or analytcs of the sample missed by initial nanoLC/MS experiments. For example, previously identified components of the sample can be excluded from the data dependent acquisition during the subsequent infusion experiment (from the portion stored in the lube), therefore, infusion experiments are able to acquire MS/MS data on the lower-intensity components missed during the initial nanoLC/MS/MS experiment. In some cases, previously identified components of the sample can be included in data dependent acquisition (and others excluded) during the subsequent infusion experiment to further analyze those components in more detail.
A number of embodiments of the invention have been described. Nevertheless, it will be understood that various modifications may be made without departing from the spirit and scope of the invention. For example, the ancillary control device 90 in FIG 3C can be a pressurized vessel or a pump to introduec gas segments or non-mixing liquid segments into the eaptured portion to provide diffusion barriers and limit diffusion of analytcs. The gas and non- mixing liquid arc immiscible with the mobile phase of the LC effluent.
In some embodiments, the split ratio of the LC effluent can be fixed or varied during the division process, e.g., according to the different abundances of analytes, by adjusting the backpressure of the output ports. For example, if analytc A is 10 times as much as analyte B in the sample, when they are separated in the LC column, split ratio of effluent with analyte A may be set to 1 : 10 while split ratio of effluent with analyte B may be set to 1 : 1.
In some embodiments, LC effluent directed to the capture capillary could be segmented and fraction collected into individual tubes (e.g., capillaries) with a tapered end on which a nanoESl sprayer could be formed. For example, each of N capillary tube can be connected to a port of a 1 :N splitter.
In some embodiments, LC effluent can be divided to more than two portions and at least two portions are captured and stored in individual tubes (e.g., capillaries). For example, as shown in FIGS. 5A and 5B, the splitter 14 can be a ten-port valve. Arrows in these figures indicate flow directions of the analytes. In its 'splitting and capture' mode, as illustrated in FlG 5A, the valve first splits the LC effluent from column 12 to two flows at port 10 with a first flow to port 1 then the mass spectrometer 18 and a second flow to port 9 which splits the flow again so that one portion of the second ilow is captured in tube 16A while the other portion of the second flow is directed to port 8 and captured in tube 16B. The split adjuster 50 controls the split ratio of the first and second flow. In the 'infusion' mode, as illustrated in FIG 5B, the captured portions in tubes 16A and 16B are driven to pass out of the tubes for analysis by the mobile phase of the column 12 connected to the pump 40. Or in another example, the splitter 14 can be a valve assembly that includes a ten-port valve 14A and a six-port valve 14B connected by two capture tubes 16A and 16B, as illustrated in FIGS. 6A-6C. Arrows in these figures indicate flow directions of the analytes. Compared to a single multi-port valve, this valve assembly configuration enables individual controls over the flow rates of the individual captured portions thus enables control over both the split ratio of the initial LC effluent and the split ratio of the primary captured portion that is further split into at least two subsidiary captured portions. Referring particularly to FlG 6A, as in the 'splitting and capture' mode, the ten-port valve 14A first splits the LC effluent from column 12 to two flows at port 10 with a first flow to port 1 then the mass spectrometer 18 and a second flow to port 9 which splits the flow again so that one portion of the second flow is captured in tube 16A while the other portion of the second flow is directed to port 8 and captured in tube 16B. Two split adjusters 50a and 50b that are in fluid communication with individual captured portions control the backpressures thus the flow rates in the capture tubes. The flow rate ratio of captured portions in tube 16A and 16B can be selected by controlling split adjusters 50a and 50b with respect to each other while the split ratio of the LC effluent (split to first and second flows) can be adjusted by controlling cither or both of two split adjusters. Referring to FIGS. 6B and 6C, as in the 'infusion' mode, cilher the captured portion in tube 16A or the portion in tube 16B may be redirected to a mass spectrometer for analysis while the other captured portion can be kept in the tube for later analysis.
In some embodiments, one portion of the effluent of a nanoLC column is driven to the mass spectrometer while another portion is captured by a capillary tube. Referring to FIG 7A, the effluent passes from the autosamplcr 30 into the LC column 12 and into the splitter 14. A first portion of the effluent passes into a second, smaller ID column 70 and then passes through a coupling device 80a that connects to a nanospray chip I I O with multiple channels. A second portion of the effluent progresses from the splitter 14 through a capture capillary 80b. The capture capillary 80b consists of a long capillary with a second chip coupling device at its end, which can be coupled to the chip 1 10 (but is not coupled in FIG 7A). After the nanoLC run has ended, the capture capillary 80b couples to the channel of the micro chip 110 through the coupling mechanism.
The effluent can be directed into column 70 or into capillary tube 80b by controlling the back pressures of the output ports of the splitter. Factors that influence back pressure include the inner diameters and the lengths of the output ports as well as the tubes connected to them. In some embodiments, the inner diameters of the output ports and/or the tubes connected to them can be about 5 microns to 750 microns, e.g., 10 to 500 microns, 20 to 200 microns, or 50 to 100 microns. For example, in a particular embodiment, the port leading to column 70 can have an i.d. of 15 microns and 15 centimeters of total tubing length while the capillary 80b can have an i.d. of 50 microns and 15 centimeters of total tube length to achieve a flow rate ratio of 1 :3. Back pressure can also be affected by applying an external pressure to the split portions via, e.g., a spit adjustor. Referring to FlG 7B, in some embodiments, the second portion passes from splitter 14 through capillary 80c and into the 6 port valve 60, where it flows through two connected channels (e.g., channels 1 and 6) into the capillary 80b. The flow of the second portion can be controlled by using a pressure bomb 120 that is connected, e.g., to channel 5. The pressure bomb 120 is a chamber that can be equipped with a small gas cylinder, a high pressure gauge, and a thick-walled metal chamber. The pressure bomb can drive the captured portion of LC effluent to the MS device 18. The flow rate can also depend on the tubing i.d. and length.
Referring to FlG 7C, attcr the nanoLC run has ended, the valve 60 switches to a second mode that connects the two ports with the pressure bomb 120 and the capture capillary. At the same time, the capture capillary 80b couples to the channel of the micro chip 110 through the coupling mechanism.
A person of skill in the art will appreciate that the additional techniques of temperature control and diffusion control, described earlier in the application, can be combined with the embodiments involving an effluent that is separated into multiple portions. All publications, patent applications, patents, and other references mentioned herein including the appendix, arc incorporated by reference herein in their entirety.
Still other embodiments are within the following claims.

Claims

WHAT IS CLA IM ED IS:
1. A liquid chromatography system, comprising: u chromatographic column through which an effluent passes, wherein the effluent comprises a plurality of analytcs that correspond to a plurality of chromatographic peaks and an elucnt; a post-column splitter having at least two output ports through which the effluent of the column is split to ut lcust a first portion and a second portion; a mass spectrometer configured to receive the first portion from a first of the output ports for analysis; and a tube connected to a second of the output ports configured to prevent substantial evaporation of the cluent in the second portion, having a plurality of separated analytes corresponding to at least two chromatographic peaks, until undergoing mass spectrometry'.
2. The system of claim 1 , configured to direct the second portion to the mass spectrometer after the first portion is analyzed by the mass spectrometer.
3. The system of claim 1 , further comprising a pump connected to the tube to pump the second portion to the mass spectrometer after the first portion is analyzed by the mass spectrometer.
4. The system of claim 1 , further comprising a second detector configured to receive the second portion from the tube after the first portion is analyzed by the mass spectrometer.
5. The system of claim 4, wherein the second detector comprises a mass spectrometer.
6. The system of claim 4, wherein the second detector comprises an infusion nanoESl/MS device.
7. The system of claim 1. wherein the tube is configured to substantially reduce the diffusion of the analytcs in the effluent stored in the tube.
8. The system of claim I , wherein the tube is configured to stay at a temperature lower than the room temperature.
9. The system of claim I . wherein the tube comprises an electrolysis electrode to clcctrolyze the eluent to produce a gas segment between any two eluent segments.
10. The system of claim 9, wherein the electrolysis is triggered by an analytical device.
1 1. The system of claim 10, wherein the device is an ultraviolet detector, fluorescence detector, an electrochemical detector, evaporative light scattering detector, nuclear magnetic resonant spectrometer, charged aerosol detector, refractive index detector, or a mass spectrometer.
12. The system of claim 1 , wherein the mass spectrometer comprises an electrospray sprayer.
13. The system of claim 1 , wherein the mass spectrometer comprises an ESI/MS device.
14. The system of claim 1 , wherein the mass spectrometer comprises an infusion nanoESI/MS device.
15. The system of claim 14, wherein the infusion nanoESI/MS device comprises a nanoESI sprayer.
16. The system of claim 15, wherein the nanoESI sprayer comprises a pulled tip of a fused silica capillary.
1 7. The system of claim 14, \s herein the infusion nanoESI/MS device comprises a chip containing an array of nanoelcctrospray nozzles.
18. The system of claim 1 , wherein the tube comprises a fused silica capillary.
19. The system of claim 1 , wherein the tube has a diameter of 250 μm or less.
20. The system of claim 1 , wherein the tube has a diameter of 100 μm or less.
21. The system of claim 1 , wherein the tube has a diameter of 75 μm or less.
22. The system of claim 1 , wherein the tube has a diameter of 50 μm or less.
23. The system of claim 1 , wherein the tube has a length of about I meter or more.
24. The system of claim 1 , wherein the tube has a length of about 10 meters or less.
25. The system of claim 1 , wherein the tube has a length of about 6 meters.
26. The system of claim 1 , wherein the second portion is directed for mass spectrometry at a lower flow rate than the first portion is.
27. The system of claim 1 , wherein the splitter comprises a T-shape piece that creates a volume ratio of about 4: 1 to about 1 : 1 of the second portion to the first portion.
28. The system of claim 1 , wherein the splitter comprises a valve that has at least five ports, a first connector connecting two of said ports, and a second connector connecting three or more of the rest said ports to split the effluent.
29. The system of claim 28, wherein the valve has at least six ports.
.
30. The system of claim 28, wherein the valve has at least one port connected to a flow controller.
31. The system of claim 28, wherein the valve has two ports that are connected by the tube.
32. The system of claim 28. wherein the valve is switchable between at least two configurations, including a first configuration in w hich the second connector connects J first set of three ports, and a second configuration in which the second connector connects a second set of ports different from the first set.
33. The system of claim I , wherein the analytes in the second portion exit the tube in the same order in which the analytes exit the chromatographic column.
34. The system of claim 1 , wherein the analytes in the second portion exit the tube in a reversed order in which the analytes exit the chromatographic column.
35. The system of claim 1 , wherein the second portion is mixed with a stream of liquid before the portion undergoes mass spectrometry.
36. The system of claim 1 , wherein the second portion has a plurality of separated analytes corresponding to at least half of the plurality of chromatographic peaks corresponding to the analytes that pass through the chromatographic column.
37. The system of claim 36, wherein the second portion has a plurality of separated analytes corresponding to at least 90% of the plurality of chromatographic peaks corresponding to the analytes that pass through the chromatographic column.
38. The system of claim 1 , further comprising a second chromatographic column, wherein the inner diameter of the second column is smaller than that of the first column.
39. The system of claim 28, further comprising a second chromatographic column, wherein the inner diameter of the second column is smaller than that of the first column.
40. A method of characterizing an analyte in a sample, the method comprising: passing an effluent computing a plurality of analytcs and an eluent through d chromatographic column, the analytes corresponding to a pluiahty of chromatographic peaks, splitting at least a first portion and a second portion of the effluent from lespeetivc output ports of a post-column splitter, the fiist portion being directed from a first of the output ports to a mass spectrometer for analysis; and receiving the second portion ha\ ing a plurality of separated analytes corresponding to at least two chromatographic peaks in a tube connected to a second of the output ports to prevent substantial evaporation of the eluent before undergoing mass spectrometry
41. The method of claim 40, further comprising directing the second portion from the tube to the mass spectrometer after the first portion is analyzed by the mass spectrometer
42. "1 he method of claim 40, further compπsing directing the second portion from the tube to a second mass spectrometer after the first portion is analyzed by the mass spectrometer
43 The method of claim 40, further comprising analyzing a first analyte from the stored second portion after a second analyte from the first portion has been analyzed by the mass spectrometer, wherein the first analyte passed out of the chromatographic column before the second analyte passed out of the chromatographic column.
44 The method of claim 40, further compπsing analyzing a first analyte from the stored second portion after a second analyte from the second stored portion has been analyzed by the mass spectrometer, wherein the first analyte passed out of the chromatographic column before the second analyte passed out of the chromatographic column.
45 The method of claim 40, further comprising analyzing a first analyte from the stored second portion before a second analyte from the second stored portion has been analyzed by the mass spectrometer, wherein the first analyte passed out of the chromatographic column before the second analyte passed out of the chromatographic column
46 The method of claim 40, further comprising cooling the second portion to substantially reduce diffusion of the analytcs in the eluent captured in the tube 47 The method ot claim 40, further comprising segmenting the stored second portion into a least two segments m the tube by a gas bubble wherein the gas bubble creates a diffusion boundary to the analytcs in the portion
48 The method of claim 47, w herein the gas bubble is formed by electrolysis of the fluent of the second portion
49 The method of claim 47, further comprising recording the segment positions in the tube by counting gas bubbles
50 The method ot claim 40, further comprising segmenting the stored second portion into a least two segments in the tube by a non-mixing liquid segment wherein the non-mixing liquid segment creates a diffusion boundary to the analytes in the portion
51 The method of claim 40, further comprising directing the stored second portion in the tube to the mass spectrometer at a calibrated flow rate controlled by a pump connected to the tube
52 The method of claim 51 , wherein the calibrated flow rate less is than 5,000 nL/min
53 The method of claim 51 , w herein the calibrated flow rate less is than 1 ,000 nL/min.
54 The method of claim 51 , wherein the calibrated flow rate less is than 2nL/min
55 The method of claim 40, wherein the second portion has a pluiahty of separated analytcs corresponding to at least half of the plurality of chromatographic peaks corresponding to the analytcs that pass through the chromatographic column
56 The method of claim 55, wherein the second portion has a plurality of separated analytcs corresponding to at least 90% of the plurality of chromatographic peaks corresponding to the analytcs that pass through the chromatographic column 57 The method of claim 40, further comprising directing the effluent into a second ehi umutogruphic column
58 The method of claim 57, w herein the directing is performed by controlling back pressures of the splitter by connecting J pump to a port of the splitter.
PCT/US2008/057902 2007-03-23 2008-03-21 Liquid chromatography-mass spectrometry WO2008118808A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US89669207P 2007-03-23 2007-03-23
US60/896,692 2007-03-23

Publications (1)

Publication Number Publication Date
WO2008118808A1 true WO2008118808A1 (en) 2008-10-02

Family

ID=39427367

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2008/057902 WO2008118808A1 (en) 2007-03-23 2008-03-21 Liquid chromatography-mass spectrometry

Country Status (2)

Country Link
US (1) US7797988B2 (en)
WO (1) WO2008118808A1 (en)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8115930B2 (en) 2007-12-05 2012-02-14 Alltech Associates, Inc. Methods and apparatus for analyzing samples and collecting sample fractions
US8305582B2 (en) 2009-09-01 2012-11-06 Alltech Associates, Inc. Methods and apparatus for analyzing samples and collecting sample fractions
WO2013157945A1 (en) 2012-04-19 2013-10-24 Universiteit Leiden Electroexctraction
WO2014204311A1 (en) 2013-06-19 2014-12-24 Universiteit Leiden Two-phase electroextraction from moving phases
US9086422B2 (en) 2008-12-10 2015-07-21 Alltech Associates, Inc. Chromatography systems and system components
US9133833B2 (en) 2008-12-04 2015-09-15 Alltech Associates, Inc. Methods and apparatus for moving aliquot samples of fluid
WO2015189549A1 (en) * 2014-06-12 2015-12-17 Micromass Uk Limited Staggered chromatography mass spectrometry
WO2017192404A1 (en) * 2016-05-05 2017-11-09 Baker Hughes Incorporated Diffusion chromatography fluid analysis

Families Citing this family (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2011510302A (en) * 2008-01-16 2011-03-31 シンジェンタ パーティシペーションズ アクチェンゲゼルシャフト Apparatus, system and method for mass spectrometry of a sample
US7816645B2 (en) * 2008-03-11 2010-10-19 Battelle Memorial Institute Radial arrays of nano-electrospray ionization emitters and methods of forming electrosprays
CA2764678C (en) 2009-06-04 2017-12-12 Lockheed Martin Corporation Multiple-sample microfluidic chip for dna analysis
EP2443432B1 (en) * 2009-06-19 2018-09-05 The Regents of The University of Michigan Electrospray and nanospray ionization of discrete samples in droplet format
DE102009045405A1 (en) * 2009-10-06 2011-04-14 INSTITUT FüR MIKROTECHNIK MAINZ GMBH Microfluidic structure and method for positioning a fluid volume in a microfluidic system
CA2814720C (en) 2010-10-15 2016-12-13 Lockheed Martin Corporation Micro fluidic optic design
US8729502B1 (en) 2010-10-28 2014-05-20 The Research Foundation For The State University Of New York Simultaneous, single-detector fluorescence detection of multiple analytes with frequency-specific lock-in detection
WO2012058632A1 (en) * 2010-10-29 2012-05-03 Thermo Fisher Scientific Oy Automated system for sample preparation and analysis
US9625429B2 (en) * 2010-10-29 2017-04-18 Cohesive Technologies Inc. LC-MS configuration for purification and detection of analytes having a broad range of hydrophobicites
WO2012129076A1 (en) * 2011-03-23 2012-09-27 Idex Health & Science Llc Valve and splitting system for multi-dimensional liquid analysis
US9322054B2 (en) 2012-02-22 2016-04-26 Lockheed Martin Corporation Microfluidic cartridge
US9977028B2 (en) 2012-11-07 2018-05-22 Ohio University Ionization of chemicals in mixture at low pH by ambient ionization/mass spectrometry
US10290479B2 (en) 2012-11-07 2019-05-14 Ohio University Online monitoring of fuel cell reactions by desorption electrospray mass spectrometry
WO2014132687A1 (en) * 2013-02-27 2014-09-04 株式会社島津製作所 Autosampler
WO2015009326A1 (en) * 2013-07-16 2015-01-22 Ohio University Versatile ambient ionization-based interface for lc/ms
GB2544135B (en) 2014-02-12 2021-03-10 Idex Health & Science Llc Volumetric flow regulation in multi-dimensional liquid analysis systems
JP6365292B2 (en) * 2014-12-19 2018-08-01 株式会社島津製作所 Ion chromatograph apparatus, ion chromatograph, ion component analysis method and electrolyte solution generation method
US9945762B2 (en) * 2014-12-30 2018-04-17 Agilent Technologies, Inc. Apparatus and method for introducing sample into a separation unit of a chromatography system without disrupting a mobile phase
CH710967B1 (en) * 2015-04-13 2019-12-13 Fatzer Ag Drahtseilfabrik Testing and monitoring system for a cable car, in particular for the urban transport of people and goods, and a method for operating the same.
US10718745B2 (en) * 2015-11-09 2020-07-21 Thermo Finnigan Llc Systems and methods for ionization
US11307181B1 (en) * 2018-07-14 2022-04-19 Sielc Technologies Corporation HPLC system with mixed-mode columns for measuring charged analytes in complex mixtures
US11393666B2 (en) 2019-12-19 2022-07-19 Thermo Finnigan Llc Automatic MS-N characterization of mass spectrometric “dark matter”
DE102020105846B4 (en) 2020-03-04 2021-12-30 Dionex Softron Gmbh Surface wave atomizer detector, its use and liquid chromatography system
US11764049B2 (en) * 2020-04-14 2023-09-19 Waters Technologies Corporation Coaxial introduction of calibrant in a flow path with analyte to an ion source

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6106710A (en) * 1999-09-10 2000-08-22 Agilent Technologies, Inc. Fraction collection delay calibration for liquid chromatography
JP2000249694A (en) * 1999-02-26 2000-09-14 Shimadzu Corp Liquid chromatograph-sampling device
DE102005025499A1 (en) * 2005-06-03 2006-12-21 Bruker Daltonik Gmbh Mass spectrometric analysis of substance mixtures by measuring directly partial flow of separated substances by mass spectrometer to obtain mass spectra series, and measuring further partial flow(s) mass spectrometrically with delay in time

Family Cites Families (72)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4670404A (en) 1985-04-22 1987-06-02 Fike Corporation Micro-scale chemical process simulation methods and apparatus useful for design of full scale processes, emergency relief systems and associated equipment
PL264094A1 (en) 1987-02-13 1988-09-29 Ceramic lining for high-temperature chemical reactors
ATE112978T1 (en) 1988-10-10 1994-11-15 Commw Scient Ind Res Org METHOD AND DEVICE FOR CONTINUOUS CHEMICAL REACTIONS.
EP0724480B1 (en) 1993-10-18 1997-11-19 Imperial Chemical Industries Plc Catalytic process
US5580523A (en) 1994-04-01 1996-12-03 Bard; Allen J. Integrated chemical synthesizers
US6001229A (en) 1994-08-01 1999-12-14 Lockheed Martin Energy Systems, Inc. Apparatus and method for performing microfluidic manipulations for chemical analysis
DE9413553U1 (en) 1994-08-23 1994-10-13 Hewlett Packard Gmbh Connecting capillary
US5587582A (en) 1995-05-19 1996-12-24 Cornell Research Foundation, Inc. Self-aligning liquid junction
WO1997001755A2 (en) * 1995-06-26 1997-01-16 Perseptive Biosystems, Inc. High speed, automated, continuous flow, multi-dimensional molecular selection and analysis
US5856174A (en) 1995-06-29 1999-01-05 Affymetrix, Inc. Integrated nucleic acid diagnostic device
US6132580A (en) 1995-09-28 2000-10-17 The Regents Of The University Of California Miniature reaction chamber and devices incorporating same
ATE201862T1 (en) 1995-12-20 2001-06-15 Alcan Int Ltd THERMALPLASM REACTOR AND WASTEWATER TREATMENT METHOD
JP3279914B2 (en) 1996-03-29 2002-04-30 エヌケ−ケ−プラント建設株式会社 On-column FDG synthesizer
US5808020A (en) 1996-08-12 1998-09-15 Associated Universities, Inc. Optical reaction cell and light source for 18F! fluoride radiotracer synthesis
US6120666A (en) 1996-09-26 2000-09-19 Ut-Battelle, Llc Microfabricated device and method for multiplexed electrokinetic focusing of fluid streams and a transport cytometry method using same
US5858187A (en) 1996-09-26 1999-01-12 Lockheed Martin Energy Systems, Inc. Apparatus and method for performing electrodynamic focusing on a microchip
US6110343A (en) 1996-10-04 2000-08-29 Lockheed Martin Energy Research Corporation Material transport method and apparatus
AU6152498A (en) 1997-02-05 1998-08-25 California Institute Of Technology Microfluidic sub-millisecond mixers
DE19708472C2 (en) 1997-02-20 1999-02-18 Atotech Deutschland Gmbh Manufacturing process for chemical microreactors
US6235471B1 (en) 1997-04-04 2001-05-22 Caliper Technologies Corp. Closed-loop biochemical analyzers
US6391622B1 (en) 1997-04-04 2002-05-21 Caliper Technologies Corp. Closed-loop biochemical analyzers
DE19717085C2 (en) 1997-04-23 1999-06-17 Bruker Daltonik Gmbh Processes and devices for extremely fast DNA multiplication using polymerase chain reactions (PCR)
WO1998049344A1 (en) 1997-04-28 1998-11-05 Lockheed Martin Energy Research Corporation Method and apparatus for analyzing nucleic acids
US5961932A (en) 1997-06-20 1999-10-05 Eastman Kodak Company Reaction chamber for an integrated micro-ceramic chemical plant
US6036927A (en) 1997-07-22 2000-03-14 Eastman Kodak Company Micro-ceramic chemical plant having catalytic reaction chamber
US5842787A (en) 1997-10-09 1998-12-01 Caliper Technologies Corporation Microfluidic systems incorporating varied channel dimensions
US5976472A (en) 1997-10-15 1999-11-02 Eastman Kodak Company Integrated micro-ceramic chemical plant with insertable catalytic reaction chambers
US5965092A (en) 1997-10-15 1999-10-12 Eastman Kodak Company Integrated micro-ceramic chemical plant with insertable micro-filters
US6139734A (en) * 1997-10-20 2000-10-31 University Of Virginia Patent Foundation Apparatus for structural characterization of biological moieties through HPLC separation
WO1999041015A1 (en) 1998-02-11 1999-08-19 Institut für Physikalische Hochtechnologie e.V. Miniaturized temperature-zone flow reactor
US6117396A (en) 1998-02-18 2000-09-12 Orchid Biocomputer, Inc. Device for delivering defined volumes
GB9808836D0 (en) 1998-04-27 1998-06-24 Amersham Pharm Biotech Uk Ltd Microfabricated apparatus for cell based assays
GB9813421D0 (en) 1998-06-23 1998-08-19 Imp College Innovations Ltd Scintillation head
KR100433926B1 (en) 1998-07-09 2004-06-04 스톤 앤드 웹스터 인코포레이티드 Radial flow reactor
US6572830B1 (en) 1998-10-09 2003-06-03 Motorola, Inc. Integrated multilayered microfludic devices and methods for making the same
US6485692B1 (en) 1998-12-04 2002-11-26 Symyx Technologies, Inc. Continuous feed parallel reactor
US6062261A (en) 1998-12-16 2000-05-16 Lockheed Martin Energy Research Corporation MicrofluIdic circuit designs for performing electrokinetic manipulations that reduce the number of voltage sources and fluid reservoirs
US6319476B1 (en) 1999-03-02 2001-11-20 Perseptive Biosystems, Inc. Microfluidic connector
US6749814B1 (en) 1999-03-03 2004-06-15 Symyx Technologies, Inc. Chemical processing microsystems comprising parallel flow microreactors and methods for using same
US6171850B1 (en) 1999-03-08 2001-01-09 Caliper Technologies Corp. Integrated devices and systems for performing temperature controlled reactions and analyses
US6241953B1 (en) 1999-06-21 2001-06-05 Ceramic Oxides International B.V. Thermal reactor with self-regulating transfer mechanism
US6524456B1 (en) 1999-08-12 2003-02-25 Ut-Battelle, Llc Microfluidic devices for the controlled manipulation of small volumes
SE518803C2 (en) 1999-09-03 2002-11-26 Chematur Eng Ab Method and reaction system with high pressure and high temperature suitable for supercritical water oxidation
AU1476501A (en) 1999-11-09 2001-06-06 Sri International Screening and analysis of polymers, specialty chemicals and catalysts using radiography
US6440669B1 (en) 1999-11-10 2002-08-27 Agilent Technologies, Inc. Methods for applying small volumes of reagents
US6537506B1 (en) 2000-02-03 2003-03-25 Cellular Process Chemistry, Inc. Miniaturized reaction apparatus
US6706538B1 (en) 2000-02-29 2004-03-16 Boston Innovation Inc. Microvolume liquid dispensing array
US6818189B1 (en) 2000-05-05 2004-11-16 Saudi Basic Industries Corporation Tubular reactor with gas injector for gas phase catalytic reactions
US6977064B1 (en) 2000-05-05 2005-12-20 Saudi Basic Industries Corporation Apparatus for the controlled optimized addition of reactants in continuous flow reaction systems
US6599484B1 (en) 2000-05-12 2003-07-29 Cti, Inc. Apparatus for processing radionuclides
EP1309397B1 (en) 2000-08-09 2005-02-02 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. Microreactor device for solid-phase supported synthesis and microreactor system comprising individual microreactor devices
WO2002014854A1 (en) 2000-08-14 2002-02-21 Chevron U.S.A. Inc. Use of microchannel reactors in combinatorial chemistry
US6858435B2 (en) * 2000-10-03 2005-02-22 Dionex Corporation Method and system for peak parking in liquid chromatography-mass spectrometer (LC-MS) analysis
US7514046B2 (en) 2000-10-31 2009-04-07 Caliper Life Sciences, Inc. Methods and systems for processing microscale devices for reuse
AU2002307152A1 (en) 2001-04-06 2002-10-21 California Institute Of Technology Nucleic acid amplification utilizing microfluidic devices
GB0115927D0 (en) 2001-06-29 2001-08-22 Nycomed Amersham Plc Solid-phase nucleophilic fluorination
GB0115929D0 (en) 2001-06-29 2001-08-22 Nycomed Amersham Plc Solid-phase electrophilic fluorination
GB0206117D0 (en) 2002-03-15 2002-04-24 Imaging Res Solutions Ltd Use of microfabricated devices
US7244961B2 (en) 2002-08-02 2007-07-17 Silicon Valley Scientific Integrated system with modular microfluidic components
US7459128B2 (en) 2002-08-13 2008-12-02 Molecular Bioproducts, Inc. Microfluidic mixing and dispensing
US6832787B1 (en) 2003-01-24 2004-12-21 Sandia National Laboratories Edge compression manifold apparatus
US6926313B1 (en) 2003-04-02 2005-08-09 Sandia National Laboratories High pressure capillary connector
JP2006527367A (en) 2003-04-22 2006-11-30 モレキュラー テクノロジーズ インコーポレイテッド System and method for synthesizing molecular imaging probes such as FDG
JP2005065632A (en) 2003-08-26 2005-03-17 National Institute Of Advanced Industrial & Technology Method for multistep enzyme reaction and microreactor for multistep enzyme reaction
GB0320337D0 (en) 2003-08-29 2003-10-01 Syrris Ltd A microfluidic system
WO2005056872A1 (en) 2003-12-08 2005-06-23 Trex Enterprises Corp. Method of making chemical vapor composites
US7592185B2 (en) 2004-02-17 2009-09-22 Molecular Bioproducts, Inc. Metering doses of sample liquids
WO2005082535A1 (en) 2004-02-27 2005-09-09 University Of Limerick Buoyancy-driven microfluidics
US20050232387A1 (en) 2004-04-20 2005-10-20 Padgett Henry C Microfluidic apparatus and method for synthesis of molecular imaging probes
US20050252840A1 (en) * 2004-05-13 2005-11-17 Eksigent Technologies, Llc Micromixer
GB2421202B (en) 2004-12-15 2009-12-09 Syrris Ltd Modular microfluidic system
FR2884443B1 (en) 2005-04-18 2007-06-29 Inst Francais Du Petrole LABORATORY REACTOR FOR THE STUDY OF REACTIONS IN THE GAS AND LIQUID PHASE

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2000249694A (en) * 1999-02-26 2000-09-14 Shimadzu Corp Liquid chromatograph-sampling device
US6106710A (en) * 1999-09-10 2000-08-22 Agilent Technologies, Inc. Fraction collection delay calibration for liquid chromatography
DE102005025499A1 (en) * 2005-06-03 2006-12-21 Bruker Daltonik Gmbh Mass spectrometric analysis of substance mixtures by measuring directly partial flow of separated substances by mass spectrometer to obtain mass spectra series, and measuring further partial flow(s) mass spectrometrically with delay in time

Cited By (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8305581B2 (en) 2007-12-05 2012-11-06 Alltech Associates, Inc. Methods and apparatus for analyzing samples and collecting sample fractions
US8115930B2 (en) 2007-12-05 2012-02-14 Alltech Associates, Inc. Methods and apparatus for analyzing samples and collecting sample fractions
US9133833B2 (en) 2008-12-04 2015-09-15 Alltech Associates, Inc. Methods and apparatus for moving aliquot samples of fluid
US9086422B2 (en) 2008-12-10 2015-07-21 Alltech Associates, Inc. Chromatography systems and system components
US8314934B2 (en) 2009-09-01 2012-11-20 Alltech Associates, Inc. Methods and apparatus for analyzing samples and collecting sample fractions
US8305582B2 (en) 2009-09-01 2012-11-06 Alltech Associates, Inc. Methods and apparatus for analyzing samples and collecting sample fractions
US9322813B2 (en) 2009-09-01 2016-04-26 Alltech Associates, Inc. Methods and apparatus for analyzing samples and collecting sample fractions
WO2013157945A1 (en) 2012-04-19 2013-10-24 Universiteit Leiden Electroexctraction
US9919317B2 (en) 2012-04-19 2018-03-20 Universiteit Leiden Electroextraction
WO2014204311A1 (en) 2013-06-19 2014-12-24 Universiteit Leiden Two-phase electroextraction from moving phases
US11504645B2 (en) 2013-06-19 2022-11-22 Universiteit Leiden Two-phase electroextraction from moving phases
WO2015189549A1 (en) * 2014-06-12 2015-12-17 Micromass Uk Limited Staggered chromatography mass spectrometry
WO2017192404A1 (en) * 2016-05-05 2017-11-09 Baker Hughes Incorporated Diffusion chromatography fluid analysis
GB2566386A (en) * 2016-05-05 2019-03-13 Baker Hughes A Ge Co Llc Diffusion chromatography fluid analysis
GB2566386B (en) * 2016-05-05 2021-09-15 Baker Hughes A Ge Co Llc Diffusion chromatography fluid analysis

Also Published As

Publication number Publication date
US20080314129A1 (en) 2008-12-25
US7797988B2 (en) 2010-09-21

Similar Documents

Publication Publication Date Title
US7797988B2 (en) Liquid chromatography-mass spectrometry
US5917184A (en) Interface between liquid flow and mass spectrometer
US6858435B2 (en) Method and system for peak parking in liquid chromatography-mass spectrometer (LC-MS) analysis
US6139734A (en) Apparatus for structural characterization of biological moieties through HPLC separation
US8741149B2 (en) Mass spectrometer
Bonfiglio et al. The effects of sample preparation methods on the variability of the electrospray ionization response for model drug compounds
US8546752B2 (en) Solid-phase extraction (SPE) tips and methods of use
US5117109A (en) Exchange method of mobile phase in high-performance liquid chromatography mass spectrometry and its apparatus
US20070183928A1 (en) Variable flow rate system for column chromatography
US9490110B2 (en) Multi-segment injection-capillary electrophoresis-mass spectrometry (MSI-CE-MS): a multiplexed screening platform and data workflow for chemical analysis
Pelzing et al. Separation techniques hyphenated to electrospray‐tandem mass spectrometry in proteomics: Capillary electrophoresis versus nanoliquid chromatography
CN108398479B (en) Method and apparatus for isotope ratio mass spectrometry
US11624737B2 (en) Methods for detecting lacosamide by mass spectrometry
EP3155418B1 (en) Staggered chromatography mass spectrometry
Ross Capillary electrophoresis-mass spectrometry: practical implementation and applications
US20230273226A1 (en) Mass spectrometric determination of testosterone in multiplexed patient samples
JP4667056B2 (en) Mass spectrometer
Helmja et al. Fraction collection in capillary electrophoresis for various stand-alone mass spectrometers
CN109580849B (en) Method for measuring index components in traditional Chinese medicine oral liquid
Vollmer et al. Peptide enrichment by microfluidic electrocapture for online analysis by electrospray mass spectrometry
Bhosale et al. A Brief Review on Hyphenated Techniques
Silberring Analysis of neuropeptides by size-exclusion HPLC linked to electrospray ionization mass spectrometry
Shalliker et al. HPLC-Hyphenation
Mabrouk et al. Measurement of Neuropeptides in Dialysate by LC-MS
CN112119310A (en) Method for detecting chromogranin A by mass spectrometry

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 08732698

Country of ref document: EP

Kind code of ref document: A1

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 08732698

Country of ref document: EP

Kind code of ref document: A1