WO2010006605A2

WO2010006605A2 - Thrombin substrate and assay for determining the level of bioactive thrombin in a sample

Info

Publication number: WO2010006605A2
Application number: PCT/DK2009/000169
Authority: WO
Inventors: Qiu-Ping Qin; Harri Takalo; Allan Milton Byrnard; Kirsten Marie Jakobsen
Original assignee: Radiometer Medical Aps
Priority date: 2008-07-16
Filing date: 2009-07-10
Publication date: 2010-01-21
Also published as: JP2011527889A; US20100184106A1; JP5606435B2; EP2316035A2; US20130344520A1; WO2010006605A3; US8535898B2; CN102124346B; CN102124346A

Abstract

Substrates for thrombin and assays for determining the level of bioactive thrombin in a sample are disclosed. The substrate has the general formula: A-X-Z-A' wherein one of either A or A' comprises a luminescent chelate, for example a lanthanide chelate. The other one of A or A' comprises a first partner of a binding pair, for example Biotin and optionally a spacer. X forms a tri or tetra peptide, for example X'-Phe-Aze-Arg, X'-Phe-Pip-Arg and X'-Phe-Pro-Arg, wherein X is absent or selected among Lys, Ahx, lie, and VaI. Z comprises a linker, for example a diamine linker.

Description

THROMBIN SUBSTRATE AND ASSAY FOR DETERMINING THE LEVEL OF BIOACTIVE THROMBIN IN A SAMPLE

The present invention relates to novel substrates for thrombin and assays for determining the level of bioactive thrombin in a sample.

Thrombin is produced by the enzymatic cleavage of two sites on prothrombin by activated Factor X (Xa).

Thrombin converts fibrinogen to an active form that assembles into fibrin. Thrombin also activates Factor Xl, Factor V and Factor VIII. This positive feedback accelerates the production of thrombin.

Factor XIII is also activated by thrombin. Factor XIIIa is a transglutaminase that catalyses the formation of covalent bonds between lysine and glutamine residues in fibrin. The covalent bonds increase the stability of the fibrin clot.

In addition to its activity in the coagulation cascade, thrombin also promotes platelet activation, via activation of protease-activated receptors on the platelet.

In clinical practice the measurement of prothrombin time (PT), i.e. the time it takes for blood to clot, in terms of activated partial thromboplastin time (APTT) and activated clotting time (ACT), is widely used for screening for defects of coagulation pathways and for monitoring anticoagulant therapy.

In order to standardize the results of blood coagulation tests the concept of International Normalized Ratio (INR) has been devised. Each manufacturer of tissue factors gives an ISI (International Sensitivity Index) for any tissue factor they make. The ISI value indicates the comparison between a particular batch of tissue factor and an internationally standardized sample. The INR is the ratio of a patients's prothrombin time to a control sample's prothrombin time, raised to the power of the ISI value for the thromboplastin reagent used.

INR = (PT_tes,/PT_normaι) ISl There are two kinds of assays available for the measurement of PT.

One kind of assay is coagulometric, which is based on the endpoint of clot formation from fibrinogen to fibrin conversion. The results of the assays are, however, variable, and particularly affected by interference with the fibrinogen/fibrin conversion in patients. Another kind of assay is non-coagulometric and is based on the use of synthetic substrates suitable for thrombin cleavage. The results of the latter assays are less variable and not affected by the fibrinogen level.

US 4,061 ,625 discloses chromogenic thrombin substrates of the formula

D-Phe - cyclic imino acid - Arg - pNA

wherein the cyclic imino acid is selected among 2-azetidine carboxylic acid, proline, 2- piperidine carboxylic acid, and pNA is p-nitroanilide. Said substrates are described as suitable for a quantitative determination of thrombin or for a study of reactions in which thrombin is formed, inhibited or consumed, or for determination of factors which exert an influence or take part in such reactions e.g. for determination of anti-thrombin, prothrombin and heparin.

When chromogenic substrates are used, the reaction is detected at approximately 405 nm. At this wavelength whole blood can not be analysed, due to the absorption from the whole blood in its self. Chromogenic substrates are therefore not suitable when the used sample type is whole blood.

Time-resolved luminescence spectroscopy using chelates such as lanthanide chelates has for several years been applied in immunoassays and DNA hybridization assays. Due to the absorption properties of whole blood, this chelate detection technology, is suitable when the sample is whole blood, compared to the chromogenic substrates, because it is possible with this technology to measure absorbance at 615 nm, at which wavelength, whole blood absorption is low.

Such chelates are described in US 7,018,851 B1 which discloses improved fluorescent lanthanide chelates which are suitable for time-resolved fluorometric (TRF) applications. The chelates are used in specific bioaffinity based binding assays such as immunoassays.

TRF is a very suitable detection technology for assays requiring high sensitivity and wide dynamic range. In immunoassay techniques using conventional fluorescence detection, high non-specific background caused by light scattering, e.g. from the biological components of the sample is a severe limitation to the sensitivity of the assay.

The fluorescent lanthanide chelates have traditionally been used in immunoassays where the detection principle is based on the capture of such chelates and detection thereof. In contrast they have not been used in enzymeassays, where the detection principle is based on cleavage of the chelate substrate and detection of the captured (not cleaved substrate) remaining in the assay.

The key feature of such a system is the provision of a substrate which is on the one hand stable and on the other hand specifically cleavable by thrombin.

Therefore there exists a need for an enzyme substrate which is specifically cleavable by thrombin and which comprises an intrinsic stable luminescent component having a long lifetime thus facilitating detection in whole blood and resulting in less interference.

Furthermore there exists a need for an assay which is fast, simple and easy to perform, subject to low variability, can easily be automated, and is of low cost.

Surprisingly it has been found that by combining, via a certain linker, a peptide which is specifically cleavable by thrombin, with a luminescent chelate, a stable substrate with a long lifetime which can be used when the sample type is whole blood is provided.

In a first aspect the present invention is a substrate for thrombin having the general formula:

A - X - Z- A'

wherein one of either A or A' comprises a luminescent chelate, and

the other one of A or A¹ comprises a first partner of a binding pair, optionally including spacer, and connected via a peptide bond to the remaining part of the substrate,

X forms a tri- or tetra-peptide selected among X' - Phe - Aze - Arg, X' - Phe - Pip - Arg, and X' - Phe - Pro - Arg, wherein

X' is absent or selected among Lys, Ahx, lie, and VaI,

Z is NH-R-Z', wherein

R is selected from the group consisting of Ci-₆alkylene, d-₆alkylenoxy, C₁- ₆thioalkylene, d-₆thioalkylenoxy, carbonyl-Gi-₆alkylene, carbonyl-d-₆alkylenoxy, C₁- ₆alkylene-carbonyl, d-₆alkylenoxy-carbonyl, d-₆alkylene-arylene, d-₆alkylenoxy- arylene, d-₆alkylene-NH, C_r6alkylenoxy-NH, Cr₆alkylene-NHCO, d-εalkylenoxy- NHCO, d-ealkylene-CONH, d-₆alkylenoxy-CONH, d-₆alkylene-COS, C₁- ₆alkylenoxy-COS, d-ealkylene-CONH-d-ealkylene-arylene, arylene, arylene-d- ₆alkylene, arylene-C_r6alkylenoxy, R¹ _a-arylene-(NHCO-R²)_b, R³ _c-arylene-(CONH-R⁴)_d, (R⁵-CONH)_e-arylene-R⁶ _f, and (R⁷-NHCO)_g-arylene~R⁸ _h, wherein each R¹, R², R³, R⁴, R⁵, R⁶, R⁷, and R⁸ at each occurrence is independently selected among d-ealkylene, d-₆alkylenoxy, d-₆thioalkylene, C_r6thioalkylenoxy, carbonyl-d-βalkylene, carbonyl- d-₆alkylenoxy, d-₆alkylene-carbonyl, arylene or arylene- d-₆alkylene, and each of a, b, c, d, e, f, g, and h is independently selected among integers from 0 to 6,

wherein arylene is phenylene, biphenylene or naphtylene, which phenylene, biphenylene or naphtylene is optionally mono-, di- or tri-substituted by one or more substituents selected among halogen, OH, SH, CN, NO₂, d-₆alkyl, d-₆alkoxy, or Ci- ₆alkoxycarbonyl,

Z' comprises one of N, S, and carbonyl, wherein,

when Z' comprises N, Z' is selected among thiourea ( -NH-CS-NH-), aminoacetamide (-NH-CO-CH₂-NH-), amide (-NH-CO-), methylamide (-NCH₃-CO-) or substituted- triazine-diamine (-NH-(R⁹C₃N₃)-NH-), when Z' comprises S, Z' is selected among thioether (-S-), thioacetamide (-S-CH₂-CO- NH-), disulfide (-S-S-), (-S-CO- CH₂-NH-) or (-S-(R⁹C₃N₃)-NH-) or

when Z' comprises carbonyl, Z' is selected among an amide (-CO-NH-, -CO-NCH₃-) or ester (-CO-O-),

wherein R⁹ is selected from the group consisting of hydrogen, halogen, Cτ₆alkyl, Ci- ₆thioalkyl, C_r6alkoxy, Crβthioalkoxy, aryloxy, and amino, which alkyl, thioalkyl, alkoxy, thioalkoxy or aryloxy group is optionally mono-, di- or tri-substituted and which amino group is optionally mono- or di-substituted by one or more substituents selected among halogen, OH, SH, CN, NO₂, d-βalkyl, d-₆alkoxy, or d-₆alkoxycarbonyl.

In the context of this invention a d-₆alkyl group means a straight chain or branched chain group of one to six carbon atoms, including but not limited to, methyl, ethyl, propyl, isopropyl, butyl, isobutyl, t-butyl, pentyl, and hexyl. Methyl, ethyl, propyl and isopropyl are preferred groups.

In the context of this invention a Cr₆alkylene radical means a straight chain or branched chain radical of one to six carbon atoms, including but not limited to, methylene, ethylene, propylene, isopropylene, butylene, isobutylene, t-butylene, pentylene, and hexylene. Methylene, ethylene, propylene and isopropylene are preferred radicals.

In the context of this invention a d-εalkoxy group means a straight or branched chain group of one to six carbon atoms linked to an oxygen atom, including but not limited to, methoxy, ethoxy, propoxy, isopropoxy, butoxy, isobutoxy, t-butoxy, pentoxy, and hexoxy. Methoxy, ethoxy, and propoxy are preferred groups.

In the context of this invention a d-₆alkylenoxy radical means a straight or branched chain radical of one to six carbon atoms linked to an oxygen atom, including but not limited to, methylenoxy, ethylenoxy, propylenoxy, isopropylenoxy, butylenoxy, isobutylenoxy, t-butylenoxy, pentylenoxy, and hexylenoxy. Methylenoxy, ethylenoxy, and propylenoxy are preferred radicals. Amino acid residues in the context of this invention have their conventional three-letter abbreviations. Thus Ahx stands for 2-amino hexanoic acid (norleucine), Ala stands for alanine, Arg stands for arginine, Asn stands for asparagine, Asp stands for aspartic acid, Aze stands for azetidine-2-carboxylic acid, Cys stands for cysteine, GIn stands for glutamine, GIu stands for glutamic acid, GIy stands for glycine, His stands for histidine, He stands for isoleucine, Leu stands for leucine, Lys stands for lysine, Met stands for methionine, Phe stands for phenylalanine, Pip stands for piperidine-2- carboxylic acid, Pro stands for proline, Ser stands for serine, Thr stands for threonine, Trp stands for tryptophane, Tyr stands for tyrosine, and VaI stands for valine.

In the context of this invention halogen represents fluoro, chloro, bromo or iodo.

The substrate according to the invention must be able to be attached to an immobilisation matrix in order to separate cleaved from non-cleaved/intact substrate. Thus the substrate according to the invention is terminated by a first partner of a binding pair, which in turn binds to a second partner of the binding pair. This second partner of said binding pair is immobilised on an immobilisation matrix.

The substrate according to the invention can be quickly cleaved by thrombin with excellent specificity. Its central part is a small peptide, in terms of a tri- or tetrapeptide, which is cleaved by thrombin at the scissile bond located between the Arg-moiety and the Z-moiety.

The substrate according to the invention can be used when the sample is plasma and is particularly advantageous as it is suitable when the sample is whole blood, because the substrate, due to the used chelate technology, can be detected at 615 nm.

In an embodiment according to the invention the substrate is one, wherein X' is absent, Phe is D-Phe, and Arg is L-Arg.

In an embodiment of the invention X is D-Phe-L-2-Aze-L-Arg or D-Phe-L-2-Pip-L-Arg.

These substrates have shown to provide fast cleavage kinetics and/or they are highly specific for thrombin. In an embodiment of the invention Tl is N and R is arylene, C_r6alkylene-arylene, or R¹ _a-arylene-(NHCO-R²)_b, wherein R¹ and R² are as defined above and a and b are 0, 1 or 2.

Thus substrates, wherein Z at the scissile bond comprises an aromatic moiety, has shown to provide excellent and fast cleavage kinetics.

In an embodiment of the invention Z' is a 6-substituted-1 ,3,5-triazine-2,4-diamine (NH- (R⁹C₃Na)-NH) or (S-(R⁹C₃N₃)-NH) bond, wherein R⁹ is selected from the group consisting of chloro, fluoro, ethoxy, 2-methoxyethoxy, 2-cyanoethoxy, 2,2,2- trifluoroethoxy, thiophenoxy and ethoxycarbonylthiomethoxy. Substrates according to this embodiment of the invention are especially specific for thrombin.

In an embodiment according to the invention the luminescent chelate is a fluorescent lanthanide chelate. E.g. as disclosed in US 7,018,851 B2, such luminescent lanthanide chelates providing high absorptivity at a suitable wavelength, several separate UV absorbing parts in the same ligand structure, effective energy transfer from the UV absorbing part to the lanthanide ion, a strongly chelating part to create thermodynamic stability and high kinetic stability, and a functional group allowing effective coupling of the chelate to be used as a binding reactant without destroying its binding properties, are very suitable for the present invention.

In a preferred embodiment according to the invention said lanthanide chelates A or A' are selected from:

and

Further such chelates may include e.g. stable chelates composed of derivatives of pyridine; bipyridines, terpyridines or various phenolic compounds as the energy mediating groups and polycarboxylic acids as chelating parts. In addition, various dicarboxylate derivatives, macrocyclic cryptates, calixarenes, DTPA carbostril 124 conjugate and macrocyclic Schiff bases have been disclosed in patent applications and/or patents.

In an embodiment of the invention the binding pair is selected among biotin as the first partner and streptavidin as the second partner (biotin/streptavidin), biotin/avidin, biotin/biotin acceptor peptide, and streptavidin derivative/acceptor peptide.

The above list of binding pairs is non-exhaustive and comprises any binding pair capable of immobilising the substrate according to the invention to an immobilisation matrix. Examples of commercially available binding pairs include, but are not limited to, Strep-tag or Strep-tagll/Strep-Tactin or Biotin/Biotin acceptor peptide.

In a preferred embodiment said first partner is biotin.

In a preferred embodiment said second partner is streptavidin. Immobilisation matrixes are known to a person skilled in the art and include micro wells, micro particles such as beads, e.g. made of plastic materials such as polystyrene or polypropylene, or made of glass.

In an embodiment according to the invention said first partner of a binding pair is connected to the remaining part of the substrate via a spacer. The spacer provides an improved solubility of the substrate which is particular useful for sterical reasons. Thus the role of the spacer is to solubilise the peptide/linker/chelate part of the substrate in order to reduce sterical hindrance otherwise imposed to the thrombin enzyme.

In an embodiment according to the invention the spacer is of the formula NH-R¹⁰- CONH-R¹¹ - CO - (NH - R¹² - NH)₁, wherein each of R¹⁰ , R¹¹ and R¹² is independently selected among Ci-₆alkylene, d-₆alkylenoxy, Ci-₆thioalkylene, d-ethioalkylenoxy, carbonyl-Crealkylene, carbonyl-Ci-₆alkylenoxy, Ci-₆alkylene-carbonyl, arylene or arylene-Ci-₆alkylene, wherein arylene is phenylene, biphenylene or naphthylene, which phenylene, biphenylene or naphthylene is optionally mono-, di- or tri-substituted by one or more substituents selected among halogen, OH, SH, CN, NO₂, Ci-₆alkyl, Ci- ₆alkoxy or Ci-₆alkoxycarbonyl, and i is an integer from 0 to 6,

In an embodiment according to the invention R¹⁰, R¹¹ and R¹² are identical or different straight-chained Crealkylene, arylene or arylene- Cr₆alkylene and i is 0 or 1.

Alternatively the spacer is a W-mer peptide, wherein W is an integer from 1 to 40.

In a preferred embodiment the substrates according to the invention are selected among:

SlV6a

SlV6b

S1V6C

S1V8

SlV9a

SlV9b

SlV12a

SlV12b

S1V12C

The substrate according to the invention can be used in an assay which is fast, simple and easy to perform, subject to low variability, can easily be automated, and is of low cost.

As the substrate of the subject invention provides for fast and precise assays, compared to assays of the prior art, the assay according to the invention does not require measurement of the time that is needed for absorbance to reach a certain value arbitrarily determined. Instead assay time can be fixed at a shorter time compared to prior art assays and the luminescence signal measured with time- resolved luminometry. In a preferred embodiment said luminometry is fluorometry. Even at this shorter time a more precise result is obtained. The end-point can refer to the time that is necessary to reach a state in which about 80% of the substrate molecules are cleaved by thrombin in the presence of an activator in a normal sample.

Alternatively, the end-point can also refer to the time that is necessary to reach a steady state of the cleavage reaction by thrombin in a normal sample.

Thus, in a second aspect, the present invention relates to a one-step assay method for determining the level of bioactive thrombin in a test sample comprising the steps:

a) combining, sequentially, simultaneously or substantially simultaneously, a substrate according to the present invention, an activator and said test sample, b) incubating the resulting reaction mixture to release thrombin-cleaved, chelate- containing substrate fragment and immobilising the binding partner-containing substrate fragment and non-thrombin-cleaved intact substrate on an immobilisation matrix,

c) washing off of non-immobilised, thrombin-cleaved chelate-containing substrate fragment and non-immobilised, non-thrombin-cleaved substrate, if present,

d) measuring the level of luminescent emission from immobilised intact substrate, and

e) calculating thrombin activity from the reduction of intensity of luminescent emission compared to a thrombin-free standard sample.

Thus by washing off non-immobilised, thrombin-cleaved chelate-containing substrate fragment and non-immobilised, non-thrombin-cleaved substrate, the latter being present when the binding capacity of the immobilisation matrix is less than the amount of substrate molecules, it is rendered possible to directly correlate the reduction of luminescence emission in the sample compared to the luminescence from a thrombin- free standard sample (cleavage percentage) with the thrombin activity in the sample.

Alternatively, a substrate is immobilised onto the surface of an immobilisation matrix, such as a micro well or a micro particle. Sequentially, simultaneously or substantially simultaneously, a test sample, such as whole blood or plasma, together with an activator, is added to the immobilisation matrix. The resulting reaction mixture is incubated to enable thrombin to act on the substrate, leading to the release of thrombin-cleaved, chelate-containing substrate fragment and leaving the binding partner-containing substrate fragment and non-thrombin-cleaved intact substrate still on the immobilisation matrix.

The identity of the activator used depends on the parameter PR, APTT or ACT to be determined. Non-limiting examples of activators to be used include thromboplastin, a partial thromboplastin reagent such as a phospholipid and contact activators such as silica, kaolin, celite, ellagic acid etc. The amount of bioactive thrombin, i.e. thrombin not bound to any inhibitor (e.g. antithrombin) and thus active in proteolytic activity, in the unknown sample can be determined from a standard curve for bioactive thrombin by its cleavage percentage (a decrease in luminescence intensity relative to total luminescence intensity). Subsequently, the level of bioactive thrombin can be expressed as the ratio of bioactive thrombin from a group of normal samples (n > 20) to that from an unknown sample. Said ratio is equivalent to either prothrombin time ratio (PR), if the activator used is thromboplastin, or activated partial thromboplastin time (APTT) ratio, if the activator used is a partial thromboplastin reagent (e.g. a phospholipid) and contact activator (e.g. silica, kaolin, celite, ellagic acid), or activated clotting time (ACT) ratio, if the activator used is a contact activator and the sample type used is native whole blood.

In an embodiment of the invention the addition of the test sample and activator is performed simultaneously or substantially simultaneously with the addition of the substrate to an immobilisation matrix.

The one-step assay method without prior substrate immobilisation is shown schematically in Fig.1. Fig 1 is described in details below.

This is particularly useful when the substrate in question is not well cleavable when immobilised on the immobilisation matrix, but cleavable by thrombin in the liquid phase, i.e. when the cleavage kinetics of the substrate in the liquid phase is faster than or at least equally fast as the binding partner binding kinetics. Thus both the cleavage reaction between the substrate and thrombin molecules and the binding reaction between immobilised binding partner and cleaved as well as intact substrate molecules take place during the following incubation step.

In another embodiment of the invention the addition of the test sample is performed after immobilisation of the substrate to an immobilisation matrix. The one-step assay method with prior substrate immobilisation is shown schematically in Fig. 2. Fig. 2 is described in details below. Such an assay has many advantages such as simplicity, rapidity and robustness. However, a condition thought to be a prerequisite for this embodiment is that substrates should be cleavable when immobilised on the immobilisation matrix.

Subsequently, non-immobilised, thrombin-cleaved chelate-containing substrate fragment is washed off. The luminescence emission from the immobilised intact substrate is measured and compared to the luminescence from a thrombin-free standard sample. The percentage of luminescence intensity reduction in the sample (cleavage percentage) is directly correlated with the thrombin activity in the sample.

A third aspect of the present invention relates to a two-step assay method for determining the level of bioactive thrombin in a test sample comprising the steps:

a) adding said sample and an activator to a substrate according to the invention in the liquid phase,

b) incubating the resulting reaction mixture to release thrombin-cleaved, chelate- containing substrate fragment,

c) adding the reaction mixture to an immobilisation matrix,

d) washing off of non-immobilised, thrombin-cleaved chelate-containing substrate fragment and non-immobilised, non-thrombin-cleaved substrate, if present,

e) measuring the level of luminescent emission from immobilized intact substrate, and

f) calculating thrombin activity from reduction of intensity of luminescent emission compared to a thrombin-free standard sample.

The two-step assay can advantageously be utilised when the substrate in question performs well only in the liquid phase. The two-step assay is shown schematically in Fig. 3. Fig 3 is described in details below. In this embodiment a reaction mixture comprising test sample, such as plasma or whole blood, activator and substrate is reacted in the liquid phase. Subsequently, part or all of said reaction mixture is transferred to an immobilisation matrix, where immobilisation of thrombin-cleaved substrate fragment and non-thrombin-cleaved intact thrombin takes place. After washing off of thrombin-cleaved chelate-containing substrate fragment and non-immobilised, non-thrombin-cleaved substrate, the level of luminescence from immobilised intact substrate is measured as above.

Which type of assay is chosen, one-step or two-step assay mainly depends on how difficult it is to perform a simultaneous addition of substrate, activator and sample to an immobilisation matrix. When it is difficult, a two-step assay is preferably used. When it is not difficult, a one-step assay can be used. Besides, the two-step assay has the advantage over the one-step assay that the substrate amount applied can be very high as long as substrate solubility permits.

A fourth aspect of the present invention provides the use of a substrate according to the invention for determining the level of bioactive thrombin in a sample. Thus the substrates according to the invention display excellent specificity for thrombin and can be quickly cleaved by thrombin, thus allowing the use of said substrates in an assay which is easy to perform, can be automated and provide reliable results in a short time.

In a fifth aspect the invention provides a test kit for determining the level of bioactive thrombin in a sample comprising

a) a luminescent substrate as defined above, and

b) a solid immobilisation matrix.

Even though the present substrate is adopted specifically for the thrombin case, it may as well be applied with different enzymes. Thus, applicant has realised that the combination of a tri- or tetra-peptide (X) and the subject linker (Z) may be easily cleaved by other enzymes as well. Thus, the substrate according to the present invention may be adapted to the desired application by a minor modification of the substrate, specifically by the choice of the peptide.

Different coagulation factors can be determined, such as active and inactive forms of FII, FV, FVII, FVIII, FIX, FX, FXI, FXII, as well as active and inactive forms, their fragments and combination of C1 , C2, C3, C4, C5, C6, C7, C8, C9. The enzymes myeloperoxidase (MPO), Alanine amino transferase (ALAT), Aspartate amino transferase (ASAT), Caspase-1 and Glutathione peroxidase-1 (GPx-1) can also be determined.

Thus in a sixth aspect the invention provides an enzyme substrate having the general formula:

A - X - Z- A'

wherein

one of either A or A' comprises a luminescent chelate, and

the other one of A or A' comprises a first partner of a binding pair, optionally including a spacer, and connected via a peptide bond to the remaining part of the substrate,

X forms a tri- or tetra-peptide,

Z is NH-R-Z', wherein

R is selected from the group consisting of d-βalkylene, d-₆alkylenoxy, Ci- ethioalkylene, d-₆thioalkylenoxy, carbonyl-Ci-₆alkylene, carbonyl-d-₆alkylenoxy, d- ₆alkylene-carbonyl, C_r6alkylenoxy-carbonyl, d-εalkylene-arylene, d-₆alkylenoxy- arylene, d-₆alkylene-NH, Ci-₆alkylenoxy-NH, Cr₆alkylene-NHCO, d-₆alkylenoxy- NHCO, d-₆alkylene-CONH, Ci-₆alkylenoxy-CONH, C_r6alkylene-COS, C₁- ₆alkylenoxy-COS, d-βalkylene-CONH-d-ealkylene-arylene, arylene, arylene-d- ₆alkylene, arylene-d-₆alkylenoxy, R¹ _a-arylene-(NHCO-R²)_b, R³ _c-arylene-(CONH-R⁴)_d, (R⁵-CONH)_e-arylene-R⁶ _f, and (R⁷-NHCO)_g-arylene-R⁸ _h, wherein each R¹, R², R³, R⁴, R⁵, R⁶, R⁷, and R⁸ at each occurrence is independently selected among d-₆alkylene, d-₆alkylenoxy, d-βthioalkylene, d-ethioalkylenoxy, carbonyl-d-₆alkylene, carbonyl- C^alkylenoxy, Cr₆alkylene-carbonyl, arylene or arylene- C^alkylene, and each of a, b, c, d, e, f, g, and h is independently selected among integers from 0 to 6,

wherein arylene is phenylene, biphenylene or naphtylene, which phenylene, biphenylene or naphtylene is optionally mono-, di- or tri-substituted by one or more substituents selected among halogen, OH, SH, CN, NO₂, C_r6alkyl, C₁^aIkOXy, or C₁- ₆alkoxycarbonyl,

Z' comprises one of N, S, and carbonyl, wherein,

when Z' comprises N, Z' is selected among thiourea ( -NH-CS-NH-), aminoacetamide (-NH-CO-CH₂-NH-), amide (-NH-CO-), methylamide (-NCH₃-CO-) or substituted- triazine-diamine (-NH-(R⁹C₃Na)-NH-),

when Z' comprises S, Z' is selected among thioether (-S-), thioacetamide (-S-CH₂-CO- NH-), disulfide (-S-S-), (-S-CO- CH₂-NH-) or (-S-(R⁹C₃N₃J-NH-) or

when Z' comprises carbonyl, Z' is selected among an amide (-CO-NH-, -CO-NCH₃-) or ester (-C0-0-),

wherein R⁹ is selected from the group consisting of hydrogen, halogen, Ci-₆alkyl, C₁- ₆thioalkyl, C_r6alkoxy,

aryloxy, and amino, which alkyl, thioalkyl, alkoxy, thioalkoxy or aryloxy group is optionally mono-, di- or tri-substituted and which amino group is optionally mono- or di-substituted by one or more substituents selected among halogen, OH, SH₁ CN, NO₂, Cr₆alkyl, C₁^aIkOXy, or Cr₆alkoxycarbonyl.

The invention is disclosed with reference to the drawings, wherein

Fig. 1 shows a schematic of a one-step assay method without prior substrate immobilisation,

Fig. 2 shows a schematic of a one-step assay method with prior substrate immobilisation,

Fig. 3 shows a schematic of a two-step assay method, Fig. 4 shows the reaction scheme of the synthesis of S1V6c, a substrate according to the invention,

Fig. 5 shows the reaction scheme of the synthesis of S1V12a, another substrate according to the invention, and

Fig. 6 shows a standard curve of S1 V6c and S1v9b according to the invention.

In Figure 1 , a one step assay without prior substrate immobilisation is shown schematically. The used substrate 1, according to the invention, comprises 4 parts ((1a, 1 b, 1c and 1d) (A-X-Z-A')), 1a denotes the first partner of a binding pair and 1a comprises optionally a spacer, 1b denotes a tri- or tetra-peptide, 1c denotes a linker and 1d denotes a luminescent chelate. 2 denotes the second partner of the binding pair bound to the surface of an immobilisation matrix 3. 4 denotes the presence of thrombin in the test sample (A with a high level and B with a low level of thrombin) and 5 denotes a thrombin free test sample (C).

In A which represent a high level of thrombin, the substrate 1 reacts with the test sample 4. This results in a cleaved substrate. The cleaved substrate comprises two parts; a first part (1a, 1b) and a second part (1c, 1d). (1a, 1b) immobilises to the immobilisation matrix, while the second part (1c, 1d) of the substrate is washed away. Then the emission of luminescence from immobilised intact substrate (1a, 1b) is measured and compared to the luminescence of a thrombin free sample 5 (C). The washing and measurement steps are not shown in figure 1.

Figure 1 also illustrates the one step assay with a low thrombin level (shown in B) and with a zero thrombin level (shown in C). C is used as the control.

Figure 2 illustrates a one step assay as described above, but where the addition of the test sample 4 or 5 is performed after immobilisation of the substrate 1 according to the invention to the immobilisation matrix 3.

Figure 3 illustrates a two-step assay. The first step I shows that substrate 1 reacts with the test sample 4 (with thrombin (A)) or 5 (free of thrombin (B)). This results in thrombin cleaved substrate (A) or in intact substrate (B). In step Il a part or all of said reaction mixture is transferred to an immobilisation matrix, where immobilisation of thrombin-cleaved substrate fragment (1a, 1 b) (A) and non-thrombin-cleaved intact thrombin substrate 1 (1a, 1 b, 1c and 1d) (B) takes place. After washing off of thrombin- cleaved chelate-containing substrate fragment (1c, 1d), the emission of luminescence from immobilised intact substrate 1 is measured as in the one step assay. The washing and measurements steps are not shown in figure 3.

Thus with (A) a low level of chelate (luminescence/fluorescence) is measured which represent a high level of thrombin. In contrast with (B) a high level of chelate (luminescence/fluorescence) is measured reflecting the absence of thrombin.

The present invention is described in more detail in the following, non-limiting specific examples.

For the below examples the following materials and instrumentation were used.

Materials

Sulfo-NHS-LC-LC-Biotin from Pierce, p-phenylenediamine from Acros, (7- Azabenzotriazol-1-yloxy)tripyrrolidinophosphonium hexafluorophosphate (PyAOP) from Aldrich and N-Ethyldiisopropylamine (DIPEA) from Fluka. Trifluoroacetic acid (TFA) was purchased from Riedel-de Haen and Triethylammonium acetate Buffer (TEAA) from Fluka. Acetonitrile (MeCN) used was HPLC grade from JT. Baker. DMF was purchased from Lab-Scan and dried over molecular sieves (4 A). All other chemicals used were of analytical grade.

H-Phe(D)-Pip-Arg was purchased from KJ Ross-Petersen ApS. N-terminally- Biotinylated long peptide-based D-phe-L-Aze-Arg-OH such as Biotin-(Ser-(Gly)₂)₇ D- phe-L-Aze-Arg-OH were purchased from Invitrogen. Innovin was bought from Dade- Behring, Siemens. Bovine serum albumin (BSA) was purchased from Sigma.

9-dentate europium-chelate(2,2',2",2'"-{[2-(4-lsothiocyanatophenyl)-ethylimino]- bis(methylene)bis{4-{[4-(a-galactopyranoxy)phenyl]ethynyl}-pyridine-6,2- diyl}bis(methylenenitrilo)} tetrakis(acetato)europium(lll)), wash solution and single cups coated with streptavidin were from lnnotrac Diagnostics (Finland). Low-fluorescence 12-well Maxisorp microtitration strips and single Maxisorp microtitration wells (ultraviolet-quenched) were purchased from Nunc (Denmark).

Instrumentation

Mass spectrometry (MS) was operated on a Voyager DE-PRO (MALDI TOF) from Perseptive Biosystems, using a-cyano-4-hydroxycinnamic acid as matrix. 1420 multilabel counter (Victor) from Wallac Oy, Perkin-Elmer life Sciences was used to measure time-resolved fluorescence at 615 nm when an assay was manually performed, while Aio immunoanalyser from lnnotrac Diagnostics was used to measure time-resolved fluorescence at 615 nm when an assay was semi-automatically performed.

Example 1

Synthesis of S1V6c

The synthesis of S1 V6c involves three steps starting with the use of a tripeptide comprising H-Phe(D)-Pip-Arg-OH as shown in Fig. 4. Firstly, a biotin group with a linear spacer is connected to the N-terminal alpha-amino group of the tripeptide. Then, a diamine linker, i.e., 4-phenylene-diamine, is coupled to the C-terminal carboxyl group of the tripeptide. Finally, a 9-dentate europium chelate is conjugated to the aromatic amino group of the introduced linker molecule.

Synthesis procedure

i) Biotinylation

H-Phe(D)-Pip-Arg-OH (5.0 mg, 11.6 μmol) was dissolved in PBS-buffer (pH 7.0, 1 ml). Sulfo-NHS-LC-LC-Biotin (12.0 mg, 17.3 μmol) was added and the mixture was stirred overnight at RT. The reaction mixture was purified with HPLC. Yield: 5.5 mg (54 %). MS: found 885.67, calculated 885.15.

ii) Coupling of a diamine-linker The biotinylated product from i) (2.4 mg, 2.7 μmol) was dissolved in dry DMF (0.5 ml). 4-Phenylene-diamine (1.2 mg, 10.84 μmol), PyAOP (1.7 mg, 3.3 μmol) and DIPEA (0.6 μl, 3.3 μmol) were added and the mixture was stirred overnight at RT. DMF was evaporated and the reaction mixture was purified on a HPLC Column of Thermo ODS Hypersil (size: 150 x 10 mm). A linear gradient made from A (0.1 % TFA) and B (MeCN) in 20 minutes from 5 % B to 50 % B was used for elution with a flow rate of 2.5 ml/min.

The yield was 2.4 mg (92 %). MS found (975.83) was in close agreement with MS calculated (975.28).

iii) Labelling

The product from ii) (2.0 mg, 2.1 μmol) was dissolved in 50 mM carbonate buffer (pH 9.8, 0.5 ml). 9-dentate europium-chelate (2,2',2",2'"-{[2-(4-lsothiocyanatophenyl)- ethylimino]-bis(methylene)bis{4-{[4-(a-galactopyranoxy)phenyl]ethynyl}-pyridine-6,2- diyl}bis(methylenenitrilo)} tetrakis(acetato)europium(lll)) (3.3 mg, 2.5 μmol) was added and the reaction was stirred overnight at RT. The reaction mixture was purified on a HPLC Column of Phenomenex C18 (size: 250 x 10 mm). A linear gradient made from A (20 mM TEAA) and B (20 mM TEAA + 50 % MeCN) in 30 minutes from 5 % B to 100 % B was used for elution with a flow rate of 3 ml/min. The yield was 1.3 mg (27 %).

Example 2

Synthesis of S 1V12a

The synthesis of S1V12a involves only two steps (see Fig. 5) as the starting material already contains a biotin group and a spacer group made of amino acids. After the same diamine linker, i.e., 4-phenylene-diamine is coupled to the C-terminal carboxyl group of the tripeptide, a 9-dentate europium chelate is conjugated to the aromatic amino group of the introduced diamine linker molecule. The experimental conditions used for the synthesis of S1V12a were the same as those used in the relevant steps for the synthesis of S1V6c. Example 3

3 different reference standard curves to be used in subsequent thrombin determinations are constructed.

Standard curve A represent S1V6c in a concentration of 200 nM, Standard curve B represent S1V9b in a concentration of 10 nM and standard curve C represent S1V9b in a concentration of 25 mM. The substrates are prepared according to the conditions described in example 1.

Recombinant thromboplastin (Innovin) was used as activator. The assay buffer was a conventional HEPES buffer.

Standards of Thrombin concentrations from 0 to 11.9 IU/ml were applied.

The assay was performed as a two step assay. In step I the thrombin containing standards were added in different thrombin concentrations to the assay buffer together with an activator and the substrate. The reagents were mixed well and incubated at 37°C for minutes.

In step Il a part of the reaction mixture was transferred to a micro well where the capture took place. The substrate was allowed to immobilise/capture to the micro well for approximately 3 min at 37 ⁰C before washing and drying. Not captured substrate as well as the chelate containing cleaved substrate was washed away and the micro well was then dried. Finally fluorescence counts from the dried micro well were measured with a fluorescence counter.

The detected fluorescence counts are compared with a control sample free of thrombin and for constitution of the standard curve the reduction in signal compared to the reference (free of thrombin) is calculated.

The results shown in figure 6, demonstrates that increasing concentrations of S1V6c and S1 V9b results in an increased reduction of signal. This demonstrates that the substrate S1V6c and S1V9b are both very effective substrates for thrombin. S1V9b results in a higher signal reduction at lower thrombin concentration compared to S1V6b. Still however, both substrates are very suitable thrombin substrates and both can therefore be used for determining the level of thrombin in a sample. Example 4

For measurements in whole blood the standard curve in example 3 may be applied subject to the correction for the whole blood hematocrit value. Whole blood samples as well as plasma samples from 2 healthy female test persons, were tested for thrombin according to the invention.

Four independent measurements on a plasma sample from test person one, showed a reduction in the detected signal compared to the control signal of 87,7 % + 0,5%. For test person two the reduction was 91 ,5 % + 0,1%.

Similar results were obtained with whole blood samples, 80,7 % + 0,9% and 86,3 % +

0,2%, respectively, for test person one and for test person two.

The results demonstrate the ability of the substrate and the assay according to the invention to measure thrombin in whole blood as well as in plasma samples and the invariability thereof.

Claims

1. A substrate for thrombin having the general formula:

A - X - Z- A'

wherein

one of either A or A' comprises a luminescent chelate, and

X forms a tri- or tetra-peptide selected among X' - Phe - Aze - Arg, X' - Phe -

Pip - Arg, and X' - Phe - Pro - Arg, wherein

X' is absent or selected among Lys, Ahx, lie, and VaI,

Z is NH-R-Z', wherein

R is selected from the group consisting of d-₆alkylene, Cr₆alkylenoxy, C₁- 6thioalkylene, Ci-₆thioalkylenoxy, carbonyl-d-₆alkylene, carbonyl-C_r 6alkylenoxy, Ci-₆alkylene-carbonyl, d-₆alkylenoxy-carbonyl, d-₆alkylene- arylene, d-ealkylenoxy-arylene, d-₆alkylene-NH, Cr₆alkylenoxy-NH, C₁-

₆alkylene-NHCO, d-ealkylenoxy-NHCO, C_r6alkylene-CONH, C_r6alkylenoxy- CONH, d-esalkylene-COS, C_r6alkylenoxy-COS, d-ealkylene-CONH-d- 6alkylene-arylene, arylene, arylene-d-₆alkylene, arylene-d-₆alkylenoxy, R¹ _a- arylene-(NHCO-R²)_b, R³ _c-arylene-(CONH-R⁴)_d, (R⁵-CONH)_e-arylene-R⁶,, and (R⁷-NHCO)_g-arylene-R⁸ _h, wherein each R¹, R², R³, R⁴, R⁵, R⁶, R⁷, and R⁸ at each occurrence is independently selected among Cr₆alkylene, C₁- 6alkylenoxy, d-₆thioalkylene, d-₆thioalkylenoxy, carbonyl-d-₆alkylene, carbonyl-Crealkylenoxy, d-₆alkylene-carbonyl, arylene or arylene- C₁- 6alkylene, and each of a, b, c, d, e, f, g, and h is independently selected among integers from 0 to 6, wherein arylene is phenylene, biphenylene or naphtylene, which phenylene, biphenylene or naphtylene is optionally mono-, di- or tri-substituted by one or more substituents selected among halogen, OH, SH, CN, NO₂, Cr₆alkyl, C₁- 6alkoxy, or d-₆alkoxycarbonyl,

Z' comprises one of N, S, and carbonyl, wherein,

when Z' comprises N, Z' is selected among thiourea ( -NH-CS-NH-), aminoacetamide (-NH-CO-CH₂-NH-), amide (-NH-CO-), methylamide (-NCH₃- CO-) or substituted-triazine-diamine (-NH-(R⁹C₃N₃)-NH-),

when Z' comprises S, T is selected among thioether (-S-), thioacetamide (-S-

CH₂-CO-NH-), disulfide (-S-S-), (-S-CO- CH₂-NH-) or (-S-(R⁹C₃N₃)-NH-) or

when Z' comprises carbonyl, Z' is selected among an amide (-CO-NH-, -CO- NCH₃-) or ester (-C0-0-),

wherein R⁹ is selected from the group consisting of hydrogen, halogen, C₁- 6alkyl, Ci-₆thioalkyl, Crealkoxy, Ci-₆thioalkoxy, aryloxy, and amino, which alkyl, thioalkyl, alkoxy, thioalkoxy or aryloxy group is optionally mono-, di- or tri- substituted and which amino group is optionally mono- or di-substituted by one or more substituents selected among halogen, OH, SH, CN, NO₂, Crealkyl, C₁-

₆alkoxy, or Crealkoxycarbonyl.

2. The substrate according to claim 1 , wherein X is D-Phe-L-2-Aze-L-Arg or D- Phe-L-2-Pip-L-Arg.

3. The substrate according to claims 1 or 2, wherein Z' is N and R is arylene, C₁- 6alkylene-arylene, or R¹ _a-arylene-(NHCO-R²)_b, wherein a and b are O, 1 or 2.

4. The substrate according to any of the preceding claims, wherein said luminescent chelate is a fluorescent lanthanide chelate.

5. The substrate according to claim 4, wherein said lanthanide chelate is selected among

and

The substrate according to any of the preceding claims, wherein said first partner of a binding pair is a partner of a binding pair selected among biotin/streptavidin, biotin/avidin, biotin/biotin acceptor peptide, and streptavidin derivative/acceptor peptide.

7. The substrate according to any of the preceding claims, c h a r a c t e r i s e d in that said first partner of a binding pair is connected to the remaining part of the substrate via a spacer of the formula NH-R¹⁰- CONH-R¹¹ - CO - (NH - R¹² - NH)₁, wherein each of R¹⁰ , R¹¹ and R¹² is independently selected among C₁- 6alkylene, d-₆alkylenoxy, d-εthioalkylene, Crβthioalkylenoxy, carbonyl-d- 6alkylene, carbonyl-Cr₆alkylenoxy, d-ealkylene-carbonyl, arylene or arylene- Crβalkylene, wherein arylene is phenylene, biphenylene or naphthylene, which phenylene, biphenylene or naphthylene is optionally mono-, di- or tri- substituted by one or more substituents selected among halogen, OH, SH, CN, NO₂, Ci-_βalkyl, Cr₆alkoxy, or d-_δalkoxycarbonyl, and i is an integer from 0 to 6, or the spacer is a W-mer peptide, wherein W is an integer from 1 to 40.

8. The substrate according to claim 7, wherein R¹⁰, R¹¹ and R¹² are identical or different straight-chained d-βalkylene, arylene or arylene - d-₆alkylene and i is O or l

9. The substrate according to any of the preceding claims selected among S1V6(a,b,c), S1V8, S1V9(a,b) and S1V12(a,b,c)

S1V6a

S1V6b

S1V6c

S1V8

S1V9a

S1V9b

S1V12a

S1V12b

S1V12C

10. A one-step assay method for determining the level of bioactive thrombin in a test sample comprising the steps:

a) combining, sequentially, simultaneously or substantially simultaneously, a substrate according to any of the preceding claims, an activator and said test sample;

b) incubating the resulting reaction mixture to release thrombin-cleaved, chelate-containing substrate fragment and immobilising the binding partner-containing substrate fragment and non-thrombin-cleaved intact substrate on an immobilisation matrix;

c) washing off of non-immobilised, thrombin-cleaved chelate-containing substrate fragment and non-immobilised, non-thrombin-cleaved substrate, if present;

d) measuring the level of luminescent emission from immobilized intact substrate; and

11. The assay method according to claim 10, wherein the addition of said sample and activator is performed simultaneously or substantially simultaneously with the addition of the substrate to an immobilisation matrix.

12. The assay method according to claim 10, wherein the addition of said sample and activator is performed after immobilisation of the substrate to an immobilisation matrix.

13. A two-step assay method for determining the level of bioactive thrombin in a test sample comprising the steps:

a) adding said sample and an activator to a substrate according to any of claims 1-9 in liquid phase,

b) incubating the resulting reaction mixture to release thrombin-cleaved, chelate-containing substrate fragment,

c) adding the reaction mixture to an immobilisation matrix,

e) measuring the level of luminescent emission from immobilised intact substrate, and

f) calculating thrombin activity from the reduction of intensity of luminescent emission compared to a thrombin-free standard sample.

14. The assay method according to any of claims 10-13, wherein said activator is selected from the group consisting of thromboplastin, partial thromboplastin reagents and contact activators.

15. The assay method according to claim 14, wherein said partial thromboplastin reagents comprise phospholipids, and said contact activators comprise silica, kaolin, celite, ellagic acid.

16. A use of the substrate according to any of claims 1-9 for determining the level of bioactive thrombin in a sample.

17. A test kit for determining the level of bioactive thrombin in a sample comprising

a) a luminescent substrate according to any of claims 1-9,

b) a solid immobilisation matrix.

18. A substrate for an enzyme having the general formula:

A - X - Z- A'

wherein

one of either A or A' comprises a luminescent chelate, and

X forms a tri- or tetra-peptide,

Z is NH-R-Z', wherein

R is selected from the group consisting of d-ealkylene, C^alkylenoxy, C₁-

₆thioalkylene, Crethioalkylenoxy, carbonyl-Cr₆alkylene, carbonyl-d- 6alkylenoxy, Crβalkylene-carbonyl, Ci-₆alkylenoxy-carbonyl, C^ealkylene- arylene, Crβalkylenoxy-arylene, C_r6alkylene-NH, Ci-₆alkylenoxy-NH, C₁- 6alkylene-NHCO, C_r6alkylenoxy-NHCO, d-ealkylene-CONH, C_r6alkylenoxy- CONH, Crealkylene-COS, C^ealkylenoxy-COS, Crealkylene-CONH-Cr ₆alkylene-arylene, arylene, arylene-d-₆alkylene, arylene-C_r6alkylenoxy, R¹ _a- aryleπe-(NHCO-R²)_b, R³ _c-arylene-(CONH-R⁴)_d, (R⁵-CONH)_e-arylene-R⁶ _f, and (R⁷-NHCO)_g-arylene-R⁸ _h, wherein each R¹, R², R³, R⁴, R⁵, R⁶, R⁷, and R⁸ at each occurrence is independently selected among d-₆alkylene, C₁- ₆alkylenoxy, d-₆thioalkylene, d-βthioalkylenoxy, carbonyl-d-₆alkylene, carbonyl-d-₆alkylenoxy, d-₆alkylene-carbonyl, arylene or arylene- C₁- ₆alkylene, and each of a, b, c, d, e, f, g, and h is independently selected among integers from 0 to 6,

wherein arylene is phenylene, biphenylene or naphtylene, which phenylene, biphenylene or naphtylene is optionally mono-, di- or tri-substituted by one or more substituents selected among halogen, OH, SH, CN, NO₂, C_r6alkyl, C₁- ₆alkoxy, or d-ealkoxycarbonyl,

Z' comprises one of N, S, and carbonyl, wherein,

when Z' comprises S, Z' is selected among thioether (-S-), thioacetamide (-S- CH₂-CO-NH-), disulfide (-S-S-), (-S-CO- CH₂-NH-) or (-S-(R⁹C₃N₃)-NH-) or

when Z' comprises carbonyl, Z' is selected among an amide (-CO-NH-, -CO- NCH₃-) or ester (-CO-O-),

wherein R⁹ is selected from the group consisting of hydrogen, halogen, C₁- ₆alkyl, Cr₆thioalkyl, d-₆alkoxy, d-βthioalkoxy, aryloxy, and amino, which alkyl, thioalkyl, alkoxy, thioalkoxy or aryloxy group is optionally mono-, di- or tri- substituted and which amino group is optionally mono- or di-substituted, by one or more substituents selected among halogen, OH, SH, CN, NO₂, d-₆alkyl, C₁- ₆alkoxy, or d-₆alkoxycarbonyl.