WO2001042795A2 - Transferrin assay - Google Patents
Transferrin assay Download PDFInfo
- Publication number
- WO2001042795A2 WO2001042795A2 PCT/GB2000/004732 GB0004732W WO0142795A2 WO 2001042795 A2 WO2001042795 A2 WO 2001042795A2 GB 0004732 W GB0004732 W GB 0004732W WO 0142795 A2 WO0142795 A2 WO 0142795A2
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- transferrin
- content
- sample
- variants
- variant
- Prior art date
Links
- 239000012581 transferrin Substances 0.000 title claims abstract description 223
- 102000004338 Transferrin Human genes 0.000 title claims abstract description 219
- 108090000901 Transferrin Proteins 0.000 title claims abstract description 219
- 238000003556 assay Methods 0.000 title claims abstract description 42
- 238000000034 method Methods 0.000 claims abstract description 105
- 210000001124 body fluid Anatomy 0.000 claims abstract description 36
- 239000010839 body fluid Substances 0.000 claims abstract description 36
- 102000002070 Transferrins Human genes 0.000 claims abstract description 32
- 108010015865 Transferrins Proteins 0.000 claims abstract description 32
- 238000000926 separation method Methods 0.000 claims description 76
- 108010074568 disialotransferrin Proteins 0.000 claims description 52
- 108090001090 Lectins Proteins 0.000 claims description 49
- 102000004856 Lectins Human genes 0.000 claims description 49
- 239000002523 lectin Substances 0.000 claims description 49
- 239000003446 ligand Substances 0.000 claims description 47
- 108010038196 saccharide-binding proteins Proteins 0.000 claims description 39
- 210000002966 serum Anatomy 0.000 claims description 39
- 230000027455 binding Effects 0.000 claims description 31
- 102000001708 Protein Isoforms Human genes 0.000 claims description 24
- 108010029485 Protein Isoforms Proteins 0.000 claims description 24
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 15
- 238000001514 detection method Methods 0.000 claims description 7
- 239000000203 mixture Substances 0.000 claims description 7
- 125000005629 sialic acid group Chemical group 0.000 claims description 7
- 210000004369 blood Anatomy 0.000 claims description 6
- 239000008280 blood Substances 0.000 claims description 6
- 101710150766 Sialic acid-binding lectin Proteins 0.000 claims 1
- 125000000837 carbohydrate group Chemical group 0.000 claims 1
- 208000007848 Alcoholism Diseases 0.000 abstract description 9
- 201000007930 alcohol dependence Diseases 0.000 abstract description 7
- 238000012544 monitoring process Methods 0.000 abstract description 5
- 238000003745 diagnosis Methods 0.000 abstract description 4
- 108700022763 carbohydrate-deficient transferrin Proteins 0.000 description 49
- 239000000243 solution Substances 0.000 description 32
- 238000004128 high performance liquid chromatography Methods 0.000 description 27
- 150000001720 carbohydrates Chemical group 0.000 description 17
- PXIPVTKHYLBLMZ-UHFFFAOYSA-N Sodium azide Chemical compound [Na+].[N-]=[N+]=[N-] PXIPVTKHYLBLMZ-UHFFFAOYSA-N 0.000 description 16
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 12
- OWMVSZAMULFTJU-UHFFFAOYSA-N bis-tris Chemical compound OCCN(CCO)C(CO)(CO)CO OWMVSZAMULFTJU-UHFFFAOYSA-N 0.000 description 12
- 238000003127 radioimmunoassay Methods 0.000 description 12
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 12
- 235000014633 carbohydrates Nutrition 0.000 description 11
- 241000473945 Theria <moth genus> Species 0.000 description 10
- SQVRNKJHWKZAKO-UHFFFAOYSA-N beta-N-Acetyl-D-neuraminic acid Natural products CC(=O)NC1C(O)CC(O)(C(O)=O)OC1C(O)C(O)CO SQVRNKJHWKZAKO-UHFFFAOYSA-N 0.000 description 10
- 238000005342 ion exchange Methods 0.000 description 10
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 9
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- 239000007983 Tris buffer Substances 0.000 description 9
- 101000766306 Homo sapiens Serotransferrin Proteins 0.000 description 8
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 8
- 239000003153 chemical reaction reagent Substances 0.000 description 8
- 238000003018 immunoassay Methods 0.000 description 8
- 230000005291 magnetic effect Effects 0.000 description 8
- 239000002245 particle Substances 0.000 description 8
- XNSAINXGIQZQOO-SRVKXCTJSA-N protirelin Chemical compound NC(=O)[C@@H]1CCCN1C(=O)[C@@H](NC(=O)[C@H]1NC(=O)CC1)CC1=CN=CN1 XNSAINXGIQZQOO-SRVKXCTJSA-N 0.000 description 8
- SQVRNKJHWKZAKO-OQPLDHBCSA-N sialic acid Chemical compound CC(=O)N[C@@H]1[C@@H](O)C[C@@](O)(C(O)=O)OC1[C@H](O)[C@H](O)CO SQVRNKJHWKZAKO-OQPLDHBCSA-N 0.000 description 8
- 229920001213 Polysorbate 20 Polymers 0.000 description 7
- 102000023852 carbohydrate binding proteins Human genes 0.000 description 7
- 238000002474 experimental method Methods 0.000 description 7
- 238000005259 measurement Methods 0.000 description 7
- 239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 7
- 235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 description 7
- 239000000872 buffer Substances 0.000 description 6
- 238000005119 centrifugation Methods 0.000 description 6
- 238000010790 dilution Methods 0.000 description 6
- 239000012895 dilution Substances 0.000 description 6
- 235000008995 european elder Nutrition 0.000 description 6
- 239000000706 filtrate Substances 0.000 description 6
- 238000004255 ion exchange chromatography Methods 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 239000012071 phase Substances 0.000 description 6
- 238000001556 precipitation Methods 0.000 description 6
- 239000011780 sodium chloride Substances 0.000 description 6
- 239000000725 suspension Substances 0.000 description 6
- 241000283973 Oryctolagus cuniculus Species 0.000 description 5
- 238000011088 calibration curve Methods 0.000 description 5
- 108091008400 carbohydrate binding proteins Proteins 0.000 description 5
- 238000005516 engineering process Methods 0.000 description 5
- 238000001914 filtration Methods 0.000 description 5
- 239000003550 marker Substances 0.000 description 5
- 150000002482 oligosaccharides Chemical class 0.000 description 5
- 108090000765 processed proteins & peptides Proteins 0.000 description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 4
- 229910021578 Iron(III) chloride Inorganic materials 0.000 description 4
- 229920002594 Polyethylene Glycol 8000 Polymers 0.000 description 4
- 235000004443 Ricinus communis Nutrition 0.000 description 4
- 240000000528 Ricinus communis Species 0.000 description 4
- 240000006028 Sambucus nigra Species 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 238000004458 analytical method Methods 0.000 description 4
- 239000011324 bead Substances 0.000 description 4
- 238000004587 chromatography analysis Methods 0.000 description 4
- 230000003993 interaction Effects 0.000 description 4
- 229910052742 iron Inorganic materials 0.000 description 4
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 4
- 239000002609 medium Substances 0.000 description 4
- 229920001542 oligosaccharide Polymers 0.000 description 4
- 229920001223 polyethylene glycol Polymers 0.000 description 4
- -1 sheets Substances 0.000 description 4
- 230000009870 specific binding Effects 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- 108010062580 Concanavalin A Proteins 0.000 description 3
- 241000590002 Helicobacter pylori Species 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
- 102000008394 Immunoglobulin Fragments Human genes 0.000 description 3
- 108010021625 Immunoglobulin Fragments Proteins 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 3
- 241000208829 Sambucus Species 0.000 description 3
- 235000003142 Sambucus nigra Nutrition 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 229940037467 helicobacter pylori Drugs 0.000 description 3
- 238000001155 isoelectric focusing Methods 0.000 description 3
- 150000002632 lipids Chemical class 0.000 description 3
- 239000006249 magnetic particle Substances 0.000 description 3
- 230000014759 maintenance of location Effects 0.000 description 3
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 3
- 239000011976 maleic acid Substances 0.000 description 3
- 102000004169 proteins and genes Human genes 0.000 description 3
- 108090000623 proteins and genes Proteins 0.000 description 3
- 239000001509 sodium citrate Substances 0.000 description 3
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 3
- 239000006228 supernatant Substances 0.000 description 3
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 3
- NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 description 2
- QKNYBSVHEMOAJP-UHFFFAOYSA-N 2-amino-2-(hydroxymethyl)propane-1,3-diol;hydron;chloride Chemical compound Cl.OCC(N)(CO)CO QKNYBSVHEMOAJP-UHFFFAOYSA-N 0.000 description 2
- 101710186708 Agglutinin Proteins 0.000 description 2
- 241000220457 Crotalaria Species 0.000 description 2
- 238000002965 ELISA Methods 0.000 description 2
- 102000004190 Enzymes Human genes 0.000 description 2
- 108090000790 Enzymes Proteins 0.000 description 2
- 101710146024 Horcolin Proteins 0.000 description 2
- 101710189395 Lectin Proteins 0.000 description 2
- 101710179758 Mannose-specific lectin Proteins 0.000 description 2
- 101710150763 Mannose-specific lectin 1 Proteins 0.000 description 2
- 101710150745 Mannose-specific lectin 2 Proteins 0.000 description 2
- OVRNDRQMDRJTHS-KEWYIRBNSA-N N-acetyl-D-galactosamine Chemical compound CC(=O)N[C@H]1C(O)O[C@H](CO)[C@H](O)[C@@H]1O OVRNDRQMDRJTHS-KEWYIRBNSA-N 0.000 description 2
- MBLBDJOUHNCFQT-UHFFFAOYSA-N N-acetyl-D-galactosamine Natural products CC(=O)NC(C=O)C(O)C(O)C(O)CO MBLBDJOUHNCFQT-UHFFFAOYSA-N 0.000 description 2
- SQVRNKJHWKZAKO-LUWBGTNYSA-N N-acetylneuraminic acid Chemical compound CC(=O)N[C@@H]1[C@@H](O)CC(O)(C(O)=O)O[C@H]1[C@H](O)[C@H](O)CO SQVRNKJHWKZAKO-LUWBGTNYSA-N 0.000 description 2
- 108010089814 Plant Lectins Proteins 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 2
- 235000018735 Sambucus canadensis Nutrition 0.000 description 2
- 108010046516 Wheat Germ Agglutinins Proteins 0.000 description 2
- 239000000910 agglutinin Substances 0.000 description 2
- 230000002776 aggregation Effects 0.000 description 2
- 238000004220 aggregation Methods 0.000 description 2
- 206010001584 alcohol abuse Diseases 0.000 description 2
- 208000025746 alcohol use disease Diseases 0.000 description 2
- 125000003275 alpha amino acid group Chemical group 0.000 description 2
- 239000012491 analyte Substances 0.000 description 2
- 238000005349 anion exchange Methods 0.000 description 2
- 238000005571 anion exchange chromatography Methods 0.000 description 2
- 108010009577 asialotransferrins Proteins 0.000 description 2
- 235000007123 blue elder Nutrition 0.000 description 2
- 238000010168 coupling process Methods 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 235000007124 elderberry Nutrition 0.000 description 2
- 239000003623 enhancer Substances 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 239000000499 gel Substances 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 150000004676 glycans Polymers 0.000 description 2
- 239000003456 ion exchange resin Substances 0.000 description 2
- 229920003303 ion-exchange polymer Polymers 0.000 description 2
- 239000004816 latex Substances 0.000 description 2
- 229920000126 latex Polymers 0.000 description 2
- 244000005700 microbiome Species 0.000 description 2
- 239000003726 plant lectin Substances 0.000 description 2
- 229920001184 polypeptide Polymers 0.000 description 2
- 150000004804 polysaccharides Polymers 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 102000004196 processed proteins & peptides Human genes 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 238000010791 quenching Methods 0.000 description 2
- 230000000171 quenching effect Effects 0.000 description 2
- 230000002285 radioactive effect Effects 0.000 description 2
- 230000000717 retained effect Effects 0.000 description 2
- 230000035945 sensitivity Effects 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000010561 standard procedure Methods 0.000 description 2
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 1
- HNIMEQCLCNSCGH-UHFFFAOYSA-N 3-amino-5-(4-phenoxyphenyl)-1h-pyrazole-4-carbonitrile Chemical compound NC1=NNC(C=2C=CC(OC=3C=CC=CC=3)=CC=2)=C1C#N HNIMEQCLCNSCGH-UHFFFAOYSA-N 0.000 description 1
- 229920000936 Agarose Polymers 0.000 description 1
- 101710141737 Bark lectin Proteins 0.000 description 1
- 102000004506 Blood Proteins Human genes 0.000 description 1
- 108010017384 Blood Proteins Proteins 0.000 description 1
- 108010067225 Cell Adhesion Molecules Proteins 0.000 description 1
- 102000016289 Cell Adhesion Molecules Human genes 0.000 description 1
- 101000945929 Crotalaria juncea Lectin Proteins 0.000 description 1
- WQZGKKKJIJFFOK-QTVWNMPRSA-N D-mannopyranose Chemical compound OC[C@H]1OC(O)[C@@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-QTVWNMPRSA-N 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 241000588724 Escherichia coli Species 0.000 description 1
- 101000766307 Gallus gallus Ovotransferrin Proteins 0.000 description 1
- 108020004206 Gamma-glutamyltransferase Proteins 0.000 description 1
- 108090000288 Glycoproteins Proteins 0.000 description 1
- 102000003886 Glycoproteins Human genes 0.000 description 1
- 239000012630 HPLC buffer Substances 0.000 description 1
- 102000008133 Iron-Binding Proteins Human genes 0.000 description 1
- 108010035210 Iron-Binding Proteins Proteins 0.000 description 1
- 241000239218 Limulus Species 0.000 description 1
- 241001521394 Maackia amurensis Species 0.000 description 1
- 241000124008 Mammalia Species 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- SJEYSFABYSGQBG-UHFFFAOYSA-M Patent blue Chemical compound [Na+].C1=CC(N(CC)CC)=CC=C1C(C=1C(=CC(=CC=1)S([O-])(=O)=O)S([O-])(=O)=O)=C1C=CC(=[N+](CC)CC)C=C1 SJEYSFABYSGQBG-UHFFFAOYSA-M 0.000 description 1
- 241001494479 Pecora Species 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 108020004511 Recombinant DNA Proteins 0.000 description 1
- 235000003846 Ricinus Nutrition 0.000 description 1
- 241000322381 Ricinus <louse> Species 0.000 description 1
- 229920002684 Sepharose Polymers 0.000 description 1
- 238000001042 affinity chromatography Methods 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 210000004381 amniotic fluid Anatomy 0.000 description 1
- 239000003957 anion exchange resin Substances 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- BLFLLBZGZJTVJG-UHFFFAOYSA-N benzocaine Chemical compound CCOC(=O)C1=CC=C(N)C=C1 BLFLLBZGZJTVJG-UHFFFAOYSA-N 0.000 description 1
- 239000012148 binding buffer Substances 0.000 description 1
- 239000008366 buffered solution Substances 0.000 description 1
- LLSDKQJKOVVTOJ-UHFFFAOYSA-L calcium chloride dihydrate Chemical compound O.O.[Cl-].[Cl-].[Ca+2] LLSDKQJKOVVTOJ-UHFFFAOYSA-L 0.000 description 1
- 229940052299 calcium chloride dihydrate Drugs 0.000 description 1
- 238000004364 calculation method Methods 0.000 description 1
- 210000004027 cell Anatomy 0.000 description 1
- 210000001175 cerebrospinal fluid Anatomy 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000012501 chromatography medium Substances 0.000 description 1
- 230000001684 chronic effect Effects 0.000 description 1
- 238000012937 correction Methods 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 230000037029 cross reaction Effects 0.000 description 1
- ATDGTVJJHBUTRL-UHFFFAOYSA-N cyanogen bromide Chemical compound BrC#N ATDGTVJJHBUTRL-UHFFFAOYSA-N 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 229920003045 dextran sodium sulfate Polymers 0.000 description 1
- 229960000633 dextran sulfate Drugs 0.000 description 1
- 238000002405 diagnostic procedure Methods 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- KDQPSPMLNJTZAL-UHFFFAOYSA-L disodium hydrogenphosphate dihydrate Chemical compound O.O.[Na+].[Na+].OP([O-])([O-])=O KDQPSPMLNJTZAL-UHFFFAOYSA-L 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 239000012149 elution buffer Substances 0.000 description 1
- 238000011067 equilibration Methods 0.000 description 1
- 239000006167 equilibration buffer Substances 0.000 description 1
- 230000005284 excitation Effects 0.000 description 1
- 238000002875 fluorescence polarization Methods 0.000 description 1
- 239000012634 fragment Substances 0.000 description 1
- 229930182830 galactose Natural products 0.000 description 1
- 102000006640 gamma-Glutamyltransferase Human genes 0.000 description 1
- 210000004408 hybridoma Anatomy 0.000 description 1
- 230000000951 immunodiffusion Effects 0.000 description 1
- 238000000760 immunoelectrophoresis Methods 0.000 description 1
- 230000002163 immunogen Effects 0.000 description 1
- 230000001939 inductive effect Effects 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 238000012417 linear regression Methods 0.000 description 1
- 208000019423 liver disease Diseases 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 230000002906 microbiologic effect Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000004848 nephelometry Methods 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000001103 potassium chloride Substances 0.000 description 1
- 235000011164 potassium chloride Nutrition 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 102000005962 receptors Human genes 0.000 description 1
- 238000007430 reference method Methods 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 230000009450 sialylation Effects 0.000 description 1
- BBMHARZCALWXSL-UHFFFAOYSA-M sodium dihydrogenphosphate monohydrate Chemical compound O.[Na+].OP(O)([O-])=O BBMHARZCALWXSL-UHFFFAOYSA-M 0.000 description 1
- 239000012064 sodium phosphate buffer Substances 0.000 description 1
- 239000007790 solid phase Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 210000001179 synovial fluid Anatomy 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 238000012956 testing procedure Methods 0.000 description 1
- 238000004879 turbidimetry Methods 0.000 description 1
- 230000003612 virological effect Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/90—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving iron binding capacity of blood
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N2333/00—Assays involving biological materials from specific organisms or of a specific nature
- G01N2333/435—Assays involving biological materials from specific organisms or of a specific nature from animals; from humans
- G01N2333/79—Transferrins, e.g. lactoferrins, ovotransferrins
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S436/00—Chemistry: analytical and immunological testing
- Y10S436/807—Apparatus included in process claim, e.g. physical support structures
- Y10S436/808—Automated or kit
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S436/00—Chemistry: analytical and immunological testing
- Y10S436/811—Test for named disease, body condition or organ function
Definitions
- This invention relates to an assay method for assessing a transferrin variant or combination of transferrin variants for the diagnosis and monitoring of alcoholism, and to kits for performing the assay.
- the invention relates to an assay method for assessing a carbohydrate-deficient transferrin variant or any combination of such variants .
- Serum transferrin is a glycoprotein with a molecular weight of about 80 kD which comprises a single polypeptide chain with two N-linked polysaccharide chains . These polysaccharide chains are branched and each chain may terminate in either two or three antennae, each with terminal sialic acid residues.
- the asialo, monosialo and disialo variants are referred to herein as carbohydrate-deficient transferrin or CDT.
- the asialo variant, now known to be completely devoid of carbohydrate chains, is referred to herein as carbohydrate free transferrin or CFT.
- the tetrasialo variant appears to predominate; however it has been reported that the asialo, monosialo, disialo and, to some degree the trisialo variants occur in elevated levels in the blood of alcoholics (see van Eijk et al . (1983) Clin. Chim. Acta 1 ⁇ 2:167-171, Stibler (1991) Clin. Chim. 17:2029-2037 and Stibler et al . in "Carbohydrate-deficient transferrin (CDT) in serum as a marker of high alcohol consumption", Advances in the Biosciences, (Ed Nordmann et al) , Pergamon, 1988, Vol. 71, pages 353-357) .
- CDT Carbohydrate-deficient transferrin
- CDT has been shown to be an effective marker for alcohol consumption, in particular for detecting and monitoring chronic alcohol consumption, and unlike conventional tests (e.g. quantitation of ⁇ - glutamyltransferase or measurement of mean corpuscular volume) can be' used to screen for heavy alcohol intake in patients with liver disease.
- CFT carbohydrate free transferrin
- a carbohydrate-binding ligand e.g. a lectin
- the pi or charge based methods of the prior art are primarily centred on procedures involving ion exchange chromatography.
- the difference in pi between the different transferrin variants is very narrow, down to 1/10 of a pH unit and therefore to effect separation of CDT variants, a very good separation is required.
- this constraint effectively means that a column format must be used; batch filtration-based ion exchange procedures do not provide a sufficient separation or resolution.
- Column formats are however less preferred in clinical chemistry or diagnostic procedures, due to their time consuming and labour intensive operation, problems of storage and transport, incompatibility with commonly-used systems etc.
- Martensson et al (Alcoholism: Clin. and Exp. Research (1997) 21(9) : 1710-1715) describe a clinical study of transferrin variant concentrations by means of ion exchange HPLC in combination with RIA analysis of the transferrin content of the HPLC fractions eluted. Higher clinical sensitivity was found for measurement of disialotransferrin alone and with the sum of asialo-, monosialo- and disialo-transferrins compared to asialo- and monosialo-transferrins alone. A much lower clinical sensitivity was found with trisialotransferrins. Martensson et al . focus on the differences in clinical signals between the different transferrin variants with a view to selecting the best transferrin variant or combination of variants. No correlation figures for the different variants are reported.
- the present invention provides a method of producing an algorithm for determining the content of a transferrin variant or combination of transferrin variants, preferably a CDT variant or combination of CDT variants, in a sample of body fluid, said method comprising:
- the purpose of the separation step used in the methods herein described is essentially to remove all or substantially all tri-, tetra-, penta- and hexa-sialotransferrins (non-target variants) from the sample, allowing the remaining target variants (asialo-, monosialo- and disialotransferrins) to be determined
- the invention provides a method of producing an algorithm for determining the content of a transferrin variant or combination of transferrin variants, preferably a CDT variant or combination of CDT variants, in a sample of body fluid, said method comprising:
- the algorithm produced in accordance with the invention will be one capable of determining the actual content or amount of asialo- or disialo- transferrin, or the actual content or amount of asialo-, monosialo- and disialo-transferrins (i.e. CDT) in any sample of body fluid.
- the algorithm will be specific to a given determination step or separation method carried out under specific conditions.
- the algorithm for use in the invention will be based upon a quantitation of each of the isoforms of transferrin having zero, one or two sialic acid residues per molecule.
- the algorithm may be produced on the basis of the high correlation between the content of asialo- (CFT) and disialo-transferrins in a sample, preferably also the low level of monosialotransferrin .
- the invention Based on the correlation determined between asialo- and disialotransferrins, the invention essentially provides a method of producing a calibration curve specific to any given determination step or separation method and which may be used to calculate the content or amount of any transferrin variant or variants in any given sample of body fluid.
- the correlation coefficient between asialo and disialotransferrin may be determined using mathematical techniques and correlations standard in the art, e.g. least squares analysis.
- the algorithm produced in accordance with the invention may be defined by at least one of the following equations:
- T represents the determined total transferrin content in the determined fraction (or in the separated fraction following separation) ;
- A represents the actual asialotransferrin content in the sample
- D represents the actual disialotransferrin content in the sample
- CDT represents the actual total content of asialo-, monosialo- and disialotransferrins in the sample; a and b are constants defining the correlation between A and D in any serum sample; and c and d are constants specific to the determination step or separation method) .
- the invention provides a method for determining the content of a transferrin variant or combination of transferrin variants, preferably a CDT variant or combination of CDT variants, in a body fluid for use in the assessment of alcohol consumption, said method comprising:
- the separation step need not be provided if an alternative way to determine the target variants (asialo-, monosialo- and disialo- transferrins) is available. Furthermore, it is also possible to determine the content of only a portion of the target variants, so long as the portion of target variants is constant and reproducible.
- the invention provides a method for determining the content of a transferrin variant or combination of transferrin variants, preferably a CDT variant or combination of CDT variants, in a body fluid for use in the assessment of alcohol consumption, said method comprising:
- the measured transferrin variant content can be used to determine the actual levels of any transferrin variant or variants in the sample on the basis of a calibration derived from the correlation discovered for the levels of asialo- and disialotransferrins .
- the determination step or separation method used in performing the assay in accordance with the invention will be the same as that used to produce the algorithm or calibration curve, such determination steps or separation methods being performed under the same set of conditions.
- the terms "determining” or “assessing” include both quantitation in the sense of obtaining an absolute value for the amount or concentration of transferrin variant (s) in the sample, and also semi-quantitative and qualitative assessments or determinations.
- An index, ratio, percentage or similar indication of the level or amount of transferrin variant (s) for example relative to total transferrin (i.e. all transferrin variants) may be obtained.
- the assay method of the invention provides a convenient method for the determination of alcohol consumption by assaying the level of a transferrin variant or combination of transferrin variants in a body fluid, preferably a blood-derived body fluid, and may particularly find utility in the diagnosis and monitoring of alcoholism or alcohol abuse.
- the body fluid used in the assay method of the invention may be any transferrin-containing body fluid for example, synovial fluid, amniotic fluid or cerebrospinal fluid, but will generally be blood or a blood derived sample.
- the sample used for analysis will preferably be cell-free and hence, either serum or plasma may be used.
- the sample may be treated prior to being used in the assay method of the invention, for example, it may be diluted by adding a buffer or other aqueous medium.
- the purpose of the separation step used in the methods herein described is essentially to remove all or substantially all tri-, tetra-, penta- and hexa- sialotransferrins (non-target variants) from the sample, allowing the remaining target variants (asialo-, monosialo- and disialotransferrins) to be determined.
- a determination step may in a preferred embodiment be a separation step.
- this may in a preferred embodiment be a separation step.
- it may also be desirable in some circumstances to directly determine the content of the target variant (s) in a fraction of the sample without physically separating the fractions out.
- various immunoassay techniques are available which could allow detection or quantitation of target transferrin variant (s) in a body fluid.
- the antibody described in EP 0 605 627 is specific for a transferrin homolog found in alcoholics, or CDT, and therefore such an antibody may be used to determine the content of a target transferrin variant, or combination of transferrin variants.
- the antibody binds a constant fraction of the sample which is substantially free from tri- and higher sialylated transferrin it is possible to produce an algorithm in accordance with the invention.
- the determination step is effectively a direct determihation or direct measurement of the content of the target transferrin variants, or a combination of said target variants.
- Transferrin preparations which may be regarded as substantially free from tri-, tetra-, penta- and hexa- sialotransferrins are those comprising less than 20%, more preferably less than 10%, e.g. less than 5% transferrin variants having three or more sialic acid residues per molecule.
- the determination step or separation method is reproducible, separation of all asialo-, monosialo- and disialotransferrins or determination of the content of each is not required when carrying out the invention.
- clinically valuable results can be obtained by separating or determining only a fraction of these variants. What matters is that the separated or determined fraction of each variant is reproducible (i.e.
- the fraction containing the desired target variants will typically comprise at least 60%, preferably at least 70 to 80%, e.g. 90 to 95% of the asialo- and monosialo- transferrin variants present in the sample prior to separation or determination.
- the disialotransferrin content of the separated or determined fraction will generally be at least 20%, preferably up to 60 to 70%, particularly preferably 20 to 50%, e.g. about 30% of the total disialotransferrin content of the sample prior to separation or determination.
- the separated or determined fraction containing the desired target variants at least 40%, preferably at least 60%, e.g'. at least 70 to 80% of the transferrin molecules will carry a carbohydrate chain or a residue thereof .
- the separated or determined fraction will typically comprise less than 20%, e.g. 10 to 15% asialotransferrin (or CFT) , less than 5% monosialotransferrin and 70 to 80%, e.g. about 75% disialotransferrin.
- An amount of trisialotransferrin typically up to 20%, preferably up to 10%, e.g. up to 5%, can be tolerated without affecting the clinical value of the assay.
- the fraction to be determined or separated could consist essentially of asialotransferrin or it could could consist essentially of disialotransferrin, but in either case some or all of monosialotransferrin (and/or trisialotransferrin) could be present in the same fraction. Because the amount of monosialo (or trisialo-) transferrin is low relative to the amounts of asialo- and disialo- transferrin, this will not interfere significantly with the results of an assay in accordance with the invention.
- ion exchange chromatography may be used to remove all or substantially all of the tri- and higher sialylated transferrins in any of the methods herein described.
- Ion exchange as a means of separating the various isotransferrin components is well known, and is described for example in US-A-4626355 , Heil et al . (supra) and WO 96/26444.
- an anion exchange chromatography step may be used, with the chromatography conditions (e.g. pH and ion binding strength) selected to permit retention of the desired transferrin variants (e.g. hexa-, penta-, tetra- and tri-sialo transferrin, and optionally some or all of the disialo fraction) .
- Appropriate conditions e.g. buffering-capacity of the resin, sample/equilibration/elution buffer pH and/or ionic strength can readily be determined according to techniques known in the art, and according to the separation desired to be achieved.
- the sample prior to ion exchange, the sample may be treated with iron-containing buffer to saturate the iron-binding sites in the transferrin molecules in the sample.
- chloride may be used as the counterion in the ion exchange procedure in order to achieve the desired separation.
- appropriate amounts of chloride ion present in the chromatography procedure necessary to achieve retention of the desired transferrin variants may be determined by routine experiments, and may depend on the precise conditions, batch of chromatography medium etc .
- the procedure can be monitored by isoelectric focusing or HPLC analysis, again according to standard techniques known in the art .
- the ion exchange chromatography step may be carried out in any convenient manner known in the art according to choice, e.g. in a batch or column format.
- the conditions may be selected to achieve the separation (i.e.
- depletion or removal in any desired manner, for example by retaining the isotransferrin variants it is desired to remove (i.e. target variants), or by pre- treating the sample by ion exchange such that the "undesired" (i.e. non-target) variants do not absorb to the medium, and the remainder of the sample is separated and then eluted from the ion exchange medium.
- the chromatography conditions are set to permit retention of the "undesired" transferrin variants.
- ion exchange conditions which may be used, mention may be made of Whatman QASL anion exchange resin buffered at pH 6.3, which may be used to bind the trisialo and higher sialylated transferrins.
- separation of target and non-target variants may be achieved using a binding ligand capable of binding selectively either to the target or non- target transferrin variants. Any binding ligand which has an affinity for the target or non-target transferrin variants may thus be used to separate the target variants from other transferrin variants in the sample.
- the binding ligand may be a carbohydrate- binding ligand such as a lectin or mixture of lectins, e.g. as described in WO 99/00672.
- a carbohydrate- binding ligand such as a lectin or mixture of lectins, e.g. as described in WO 99/00672.
- 100% separation of CFT cannot always be achieved in practice.
- transferrin variants having a low carbohydrate content in particular monosialo- and disialo-transferrins, bind with a low affinity to carbohydrate-binding ligands, such as lectins.
- such variants bind to carbohydrate-binding ligands with a lower affinity than the transferrin variants having a higher or high carbohydrate content (i.e.
- the higher sialylated transferrins e.g. tri-, tetra- and pentasialotransferrins
- Separation methods using carbohydrate-binding ligands, for example lectins are thus effective to remove higher sialylated transferrins (e.g. tri-, tetra-, penta- and hexa-sialotransferrins) , but are generally less effective in removing lower sialylated transferrins (e.g. mono- and disialotransferrins) .
- the assay method in accordance with the invention can tolerate incomplete separation of transferrin variants without compromising the clinical value of the assay.
- the body fluid comprising transferrin variants is contacted with the carbohydrate-binding ligands, substantially all of the higher sialylated variants (tri-, tetra-, penta- and hexa-sialotransferrins) with carbohydrate side chains or remnants thereof are retained by the carbohydrate-binding ligands.
- the unbound fraction containing CFT, mono- and disialotransferrins may then be separated from the other variants and collected by any suitable means.
- the separation method comprises the steps of contacting a sample of body fluid with a carbohydrate- binding ligand, e.g. a lectin or mixture of lectins, followed by separation of a fraction not binding to said ligand.
- the total amount of transferrin in the non- binding fraction may be determined directly by measuring the transferrin not bound by the carbohydrate binding ligand. Alternatively it may be determined indirectly by determining the amount of transferrin bound to the carbohydrate binding ligand and subtracting this from the total amount of transferrin present in the sample. Generally, the direct approach is preferred.
- Any carbohydrate-binding ligand or any combination thereof may be used to separate the target variants from other transferrin variants.
- One or more carbohydrate-binding ligands may be used in the method of the invention. Where more than one ligand is being used, these may be used together or they may be used individually, for example, sequentially.
- the functional requirement of the carbohydrate binding ligand (s), rendering them suitable for use in the assay method of the present invention, is that they be capable of separating CDT from other transferrin variants.
- the carbohydrate-binding ligand will be a protein, and very many such carbohydrate-binding proteins are known in the art and are widely described in the literature.
- the carbohydrate-binding protein may, for example, be an antibody, either polyclonal or monoclonal, or may be an antibody fragment for example F(ab), F(ab') 2 or F (v) fragments.
- the antibodies or antibody fragments may be monovalent or divalent and they may be produced by hybridoma technology or be of synthetic origin, via recombinant DNA technology or chemical synthesis. Single chain antibodies could for example be used.
- the antibody may be directed or raised against any of the carbohydrate components or structures making up the Carbohydrate chains of glycosylated transferrin variants.
- an antibody reactive with or selective for sialic acid residues might be used.
- Such an antibody is used in the Sialic Acid Deficient Enzyme Immunoassay (SDT-EIA) available from Medichem, Stuttgart, Germany and described in WO 97/19355.
- the carbohydrate-binding protein may be a lectin, used singularly or in combination with other lectins or with other types of carbohydrate- binding proteins, for example, antibodies.
- Any lectin known in the art may be used in the assay method of the invention and it may be of plant, animal, microbiological or any other origin.
- the literature is replete with references to different lectins which might be used, and many may be obtained commercially, for example, from Sigma.
- carbohydrate binding proteins from microorganisms (for example, viral haemagglutinins) and higher organisms, including for example, invertebrates and mammals.
- mammalian carbohydrate binding proteins include selecting and other mammalian lectins or cell adhesion molecules (see for example Varki (1992) Current Opinion in Cell Biology 4:257-266) .
- Suitable lectins are RCA- I ⁇ Ricinus co ⁇ rmunis agglutinin) which binds terminal galactose (Kornfeld et al . (1981) J. Biol . Chem. 256:6633) or Con- A (Concanavalin A) , which is known to bind asparagine- linked oligosaccharides high in mannose .
- Other possibilities are Crotalaria juncea lectin which binds galactose residues (Ersson (1977) Biochim. Biophys.
- Lectins of varying selectivity and specificity are known. Whereas some lectins may bind to a single sugar residue in a particular location on an oligosaccharide chain, for example RCA- I (from Ricinus communis) binds only to terminal galactose residues, some may bind to complex oligosaccharide determinants for example Sambucus nigra L which binds Neu5Ac/ ( «2-6) Gal/GalNAc . All are within the scope of the present invention.
- Sialic acid binding lectins and other proteins represent a class of carbohydrate binding proteins of particular utility in the present invention (see the following, for example, for lists of suitable lectins and their sources: Mandal and Mandal (1990) Experientia 4.6:433-441) ; Zeng (1992) Z. Naturforsch, 47c:641-653 and Reuter and Schauer in Methods in Enzymology, Vol. 230, Chapter 10 at pages 196-198) .
- S. nigra L. Lectin is particularly effective when used on its own, although it may equally effectively be used in combination with other lectins eg . ConA.
- carbohydrate binding ligands useful for performance of the present invention are lectins from Helicobacter pylori and Ricinus com unis; lectins from Ricinus communis and Sambuccus nigra ; lectins from Crotalaria junctae and Sambuccus nigra; lectins from Crotalaria junctae and Helicobacter pylori and lectins from Ricinus communis and anti-sialic acid antibodies.
- the most preferred of the combinations are those which incorporate galactose- binding and sialic acid-binding ligands.
- a fraction may conveniently be collected which does not bind and which contains the CDT. Collection may be by any suitable means, for example, precipitation, centrifugation, filtration, chromatographic methods etc. Where different carbohydrate-binding ligands are used individually, different separation/collection formats may be used for each individual binding step.
- Precipitation of carbohydrate-containing moieties in the sample may be achieved using lectins having known "precipitation" properties i.e. lectins capable of inducing precipitation of the moieties to which they bind. Combinations of lectins may advantageously be used for such a precipitation procedure, since differing lectin specificities increase the number of available binding sites.
- the non-binding (CDT) fraction may then readily be collected, for example by centrifugation or filtration to separate the precipitate.
- the carbohydrate binding ligand (s) may conveniently be immobilised to facilitate the separation and collection of the non- binding fraction. It is well known in the art to immobilise carbohydrate-binding ligands such as lectins for separation purposes, for example, in chromatographic columns, and any lectin affinity chromatography method known in the art could for example be used (see for example, Cummings (1994) Methods in Enzymology 230 : 66- 86) .
- the carbohydrate-binding ligands may be immobilised by binding or coupling to any of the well known solid supports or matrices which are currently widely used or proposed for immobilisation or separation etc.
- carbohydrate-binding ligands may conveniently be coupled covalently to CNBr-activated Sepharose or N-hydroxysuccinimide- activated supports, optionally in the presence of low molecular weight haptens to protect the carbohydrate binding sites on the ligand.
- Other coupling methods for proteins are also well known in the art .
- Batch separations using immobilised carbohydrate- binding ligands may be performed using a range of different formats which are known in the art.
- the immobilised carbohydrate-binding ligands may be packed or arranged into a column.
- the body fluid comprising transferrin may be applied to the column and the transferrin variants therein contacted with the carbohydrate-binding ligands.
- the unbound fraction comprising CDT is separated from the bound fraction and collected.
- the shape and geometry of such a column may vary depending upon the carbohydrate-binding ligands used. For example, if lectins are used as the carbohydrate- binding ligands, at low lectin concentrations a long, thin column of immobilized lectins is preferred. At high lectin concentrations, column geometry is less crucial.
- Columns may be constructed using any method known in the art. If lectins are to be used as the carbohydrate-binding ligands, the columns may be constructed in either glass tubes or preferably in disposable plastic pipettes of any desired capacity. Smaller volumes may however be preferred due to economic considerations. Columns are preferably stored at around 4°C prior to use.
- the column may be flushed through with an eluant to allow or facilitate collection of the unbound fraction, in which case the eluant should preferably be administered using a calibrated micropipette to ensure the correct volume is administered.
- the volume administered is preferably within 3% of the desired (i.e. calibration) volume, more preferably, within 1 or 2%. Since the rate of binding to oligosaccharides is comparatively slow, especially with plant lectins, it is preferable that slow flow rates are employed to maximise lectin/carbohydrate interactions.
- the eluant will generally be at a temperature within 5°C of the desired (calibration) value, e.g. 25°C, and more preferably within 1°C.
- the carbohydrate- binding ligand may be immobilised on a particulate solid phase, for example, latex, silica or polymer beads.
- a particulate solid phase for example, latex, silica or polymer beads.
- magnetic beads may be used.
- the term "magnetic” as used herein means that the support is capable of having a magnetic moment imparted to it when placed in a magnetic field. In other words, a support comprising magnetic particles may readily be removed by magnetic aggregation, which provides a quick, simple and efficient way of separating the fractions following the carbohydrate binding step.
- the magnetic particles with non-target variant moieties attached may be removed onto a suitable surface by application of a magnetic field, for example, using a permanent magnet. It is usually sufficient to apply a magnet to the side of the vessel containing the sample mixture to aggregate the particles to the wall of the vessel and to collect the remainder of the sample, which will comprise the "non-binding, CDT-containing fraction" which may be returned for subsequent analysis.
- superpararaagne ic particles which include for example those described by Sintef in EP-A-106873, as magnetic aggregation and clumping of the particles during the reaction can be avoided.
- Magnetic particles are commercially available from a number of sources, including for example, Advanced Magnetics Inc., (USA), Amersham (UK), Bang Particles (USA) , and Dynal AS (Oslo, Norway) .
- Functionalised coated particles for use in the present invention may be prepared by modification of the beads, for example according to US patents 4,336,173, 4,459,378 and 4,654,267.
- beads, or other supports may be prepared having different types of functionalised surface, for attachment of a desired carbohydrate-binding ligand.
- centrifuge tube e.g. Eppendorf tube
- filter cup e.g. Eppendorf tube
- sample and carbohydrate-binding ligand may be added to the cup in the tube and allowed to bind.
- the tube (and cup) is then spun, and the non-binding supernatant collects in the tube.
- the carbohydrate- binding ligand may be such as to induce precipitation of the bound carbohydrate moieties or it may be immobilised, for example as a slurry e.g. a gel or on particles. In either case, the bound carbohydrate binding fraction is retained in the cup.
- the cup may be provided with one or more “discs” or filters which carry immobilised carbohydrate- binding ligands.
- the total content of transferrin in the separated fraction is determined. This may be done by any standard procedure known in the art for assay of transferrin, for example, by any standard immunoassay technique, e.g. an ELISA or radio- immunoassay technique. Methods for determining transferrins are described for example in US-A-4 , 626 , 355 (Joustra) .
- An example of an ELISA method could include a sandwich assay in which an immobilised antibody specific for transferrin variants which are substantially free from tri- and higher sialylated transferrins is contacted with the sample, and then enzyme-labelled anti-transferrin antibodies (available from Dako AS, Denmark) are used to detect the bound transferrin.
- a preferred such immobilised antibody is the antibody described in EP 0 605 627 and in such a case it will be appreciated that the separated fraction will be the fraction of antibody-bound transferrin and that the enzyme signal will be proportional to the total transferrin content of that fraction, allowing the total transferrin to be determined in that fraction.
- Many commercial assays for transferrin are available and have been described in the literature. For example an RID (radio immuno diffusion) assay based on the method of Mancini is available from Hoechst (see Mancini et al . Immunochemistry, 2:235-254 (1965)).
- a rocket immuno electrophoresis method is described by
- opacity will generally be generated by contacting the separated fraction or an aliquot thereof with an anti-transferrin antibody or antibody fragment, e.g. a rabbit anti-human transferrin antibody such as is commercially available from Dako of Copenhagen, Denmark.
- an anti-transferrin antibody or antibody fragment e.g. a rabbit anti-human transferrin antibody such as is commercially available from Dako of Copenhagen, Denmark.
- the Dako antibodies are specific to transferrin and show no cross reactions with other blood proteins that may be present in the eluate.
- the quantity of antibody used should of course be optimised against transferrin containing standard samples as opacification .arises from the hook effect whereby multiple transferrin binding generates the opacification centres .
- the anti-transferrin antibodies may simply be added to the tube after centrifugation .
- a polymeric opacification enhancer such as polyethyleneglycol, is preferably also added to the eluate .
- a kinetic reading mode may of course be used.
- the fraction, antibody and enhancer may be incubated for a short period, e.g. 5 minutes to an hour for end-point measurements, preferably about 10 minutes.
- the light used in the determination of opacification should have an appropriate wavelength. In this regard we have found that use of a 405 nm filter, or more preferably a 340 nm filter, yields particularly good results .
- a suitable method is to take advantage of a proximity interaction technique.
- a specific binding partner for the target transferrin variants is utilised in a proximity assay to obtain a direct determination of the amount of the target variants (asialo-, monosialo- and disialotransferrins) in the fraction (s) to be determined.
- a suitable specific binding partner is the anti-transferrin antibody which reacts selectively with transferrin homologs found in alcoholics but not in non-alcoholics, as disclosed in EP 0 605 627.
- Another means of producing a suitable specific binding partner with appropriate specificity for the target transferrin variants to be determined is to raise an antibody against a peptide immunogen which mimicks the N-glycan binding site on the transferrin molecule, for example if the peptide sequence corresponds to the amino acid sequence of human transferrin.
- the amino acid sequence of human transferrin is known and is published for example in Yang et al . , Proc . Natl . Acad. Sci. 81: 2752-2756 (1984) or accession number PO 2787 Swiss Prot database.
- FPIA fluorescence polarisation immunoassay technology
- FPIB fluorescence quenching techniques
- EMIT proximity scintillation assay
- FPIA techniques are described for example in Dandliker et al . , Immunochemistry 7: 799-828, (1970), and in Wei et al . , Anal. Chem. 65: 3372-3377 (1993)).
- Fluorescence quenching techniques are described for example in US-A-3 , 996 , 345 of Ullmann et al . , in which one binding partner carries a fluorescent residue and the other carries a quencher.
- Proximity scintillation assays are described for example in US-A-4 , 568 , 649 and EP 0 154 734 of Bertoglio- Matte . In these assays, one of the binding partners emits a short-range energy-rich radioactive signal, typically emitting ⁇ -rays, and when proximity interaction with the other binding partner occurs, a fluorophore linked to the second binding partner is excited by the radioactive energy and a fluorescent signal is generated.
- Further signal detection techniques include turbidimetry and nephelometry as described hereinbefore in relation to separation methods.
- calibration samples with known transferrin contents will also be assessed in the performance of the assay method of the invention. Such determinations can be used to plot a calibration curve from which the transferrin content of the sample under evaluation may be determined.
- Preferably calibration samples having transferrin contents of up to 0.05 mg/ml (e.g. 0.002, 0.01, 0.02 and 0.03 mg/ml) will be used.
- the total transferrin content of the determined or separated fraction containing the target variants will preferably be determined. Using an algorithm as herein described this can then be used to determine with a high degree of accuracy the content of asialo- or disialo-transferrin, or CDT content of the sample.
- the content of asialo- or disialo-transferrin or CDT may be determined as a percentage of total transferrin. This may be a more precise marker for alcohol consumption than total transferrin, and a threshold value, for example 1%, may be set. Alternatively, the presence of any transferrin variant may be assessed as an actual concentration (i.e. a mass per unit volume) .
- the invention provides a kit for a diagnostic assay according to the invention, said kit comprising: means for subjecting a sample of body fluid to a determination step or separation method capable of producing or determining the content of a fraction substantially free from tri- and higher sialylated transferrins ; means for the detection of transferrin; and means for determining the content of any transferrin variant or combination of transferrin variants in a sample of body fluid subjected to said separation method or determination step.
- the kit may also comprise a transferrin standard or standards for reference.
- the kit of the invention may comprise: at least two transferrin solutions having known asialo- and disialo- concentrations; means for subjecting a sample of body fluid to a separation method or determination step capable of producing or determining the content of a fraction substantially free from tri- and higher sialylated transferrins ; means for the detection of transferrin; and means for determining the content of any transferrin variant or combination of transferrin variants in a sample of body fluid subjected to said separation method or said determination step.
- FIG. 3 shows separation of transferrin isoforms by HPLC.
- Figures 4A and 4B show correlation of asialo vs monosialo, in A determined in % transferrin, in B determined in ⁇ g/mL.
- Figures 5A and 5B show correlation of asialo vs disialo, in A determined in % transferrin, in B determined in ⁇ g/mL.
- Figure 6 shows the correlation of (asialo-, monosialo- and disialo- transferrin) with asialo transferrin, determined in mass units ( ⁇ g/mL) .
- Figure 7 shows the correlation of (asialo-, monosialo- and disialo- transferrin) with disialotransferrin, determined in mass units ( ⁇ g/mL) .
- Figure 8 shows the correlation of asialo transferrin with (monosialo- and disialo-) transferrin, determined in % transferrin.
- Figure 9 shows the correlation of asialo- with trisialo- transferrin, determined in % transferrin.
- Figure 10 shows the correlation of (asialo-, monosialo- and disialo-transferrin) with asialotransferrin, determined in % transferrin.
- Figure 11 shows the correlation of (asialo-, monosialo- and disialo- transferrin) with disialotransferrin, determined in % transferrin.
- the transferrin variant content of lipid stripped, iron treated serum samples was analysed using a combined HPLC-RIA method.
- the levels of the different sialic acid isoforms were determined first by separation on HPLC with an i. ⁇ n exchange column.
- the asialo-, monosialo-, disialo- and trisialotransferrin fractions were collected in separate tubes.
- the higher isoforms, tetrasialo-, pentasialo- and hexasialo-transferrins were collected in a separate tube.
- the % of the different fractions was first determined using HPLC, then the concentration of the fractions was determined on a gamma counter using an immunoassay procedure as outlined below.
- Nitrilotriacetic acid trisodium salt monohydrate >98%
- Mobile phase A 20mM BisTris buffer, pH 6.5
- Mobile phase B 20mM BisTris buffer, pH 6.5 , 0.5M NaCl
- Mobile phase C 20mM BisTris buffer, pH 5.8
- Mobile phase D water
- Pre-column HP Pre-column cartridge holder 4.0mm inner diameter, filled with HQ50 in slurry form
- Transferrin calibrators (based on Seronorm calibrated serum supplied by Sero AS, Norway, diluted in mobile phase A) 0, 0.05, 0.10, 0.15,
- HPLC Pump Quaternary pump Mod.
- G1311A - HPLC Injector Autosampler Mod.
- HPLC Detector Diode Array Detector Mod.
- G1315A - Data Handling HP ChemStation pH meter: Hanna Instruments 8417
- 150 ⁇ l of each serum sample was added to 30 ⁇ l FeNTA (an aqueous solution containing 2.751 g/1 nitrilotriacetic trisodiummonohydrate and 2.703 g/1 FeCl 3 .6H 2 0 adjusted to a pH of 6.5 using 2M NaOH) and vortexed.
- the resulting solution was then added to lO ⁇ l dextran sulfate (20 mg/ml) and lO ⁇ l potassium chloride (147 mg/ml) .
- the solution was cooled to 2-8°C for 30 mins .
- the sample was then centrifuged at 3800 rpm for 10 mins.
- 150 ⁇ l of the supernatant was pipetted out and added to 900 ⁇ l HPLC buffer A.
- the sample was filtered on an acrodisc filter and then injected into the HPLC in an aliquot of 800 ⁇ l.
- the transferrin isoforms were separated by an ion- chromatographic gradient method.
- the transferrin was selectively detected spectrophotometrically at 470 nm by the HP ChemStation.
- the steps D1-D8 in the following immunoassay procedure were performed.
- the concentration was determined using calibrators from 0-2.5 ⁇ g/ml.
- the steps D1-D8 were performed with the CDTect -calibrators .
- Dl 500 ⁇ l calibrator is pipetted out.
- the calibrators are dilutions of human transferrin (obtained from Intergen) in PBS containing 1% BSA, 0.1% Tween 20 at pH 7.0)
- 125 I transferrin solution is made by dilution of 125- labelled human transferrin (obtained from Isopharma AS, Kjeller, Norway) to a concentration suitable for gamma-counting in an aqueous buffered solution containing 0.037 M disodiumhydrogen phosphatedihydrate, 0.013 M sodiumdihydrogen phosphatemonohydrate, 1% BSA, 0.1% Tween 20 and 0.03% Patent Blue.
- the antibody solution is made from rabbit anti human transferrin antiserum (obtained from BioCell, product No. 01090) diluted 1:450 in 0.4 M sodium phosphate buffer with 1% BSA, 0.1% Tween 20 at pH 7.0.
- the decanting suspension is a solution of secondary anti rabbit antibodies (obtained from Pharmacia & Upjohn, product No. 30-3794-00)
- D represents disialotransferrin content of a serum sample
- A represents asialotransferrin content of a serum sample
- At least two solutions having known levels of asialo- and disialotransferrins are subjected to a separation method capable of removing substantially all tri- and higher sialotransferrins (e.g. based on lectins or ion exchange matrices) . Thereafter the total transferrin content of the isolated fraction of transferrin is determined (e.g. by a radioimmunoassay method for transferrin quantitation) . Based on the previously determined correlation between the level of asialo- and disialotransferrins and the low level of monoasialotransferrin, the following relations can be established:
- T2 c.A2 + d.D2
- T3 c.A3 + d.D3
- Tl, T2 , T3 , etc. represent the measured total transferrin content of each sample following separation* ;
- Al, A2 , A3, etc. represent the known contents of asialotransferrin in each sample
- Dl, D2 , D3 , etc. represent the known contents of diasialotransferrin in each sample; and c and d are constants) .
- T represents measured total transferrin content
- A represents actual asialotransferrin content in the sample
- D represents actual disialotransferrin content in the sample; and a, b, c and d are each constants) .
- CDT is the total content of asialo-, monosialo- and disialotransferrin in the sample
- 20 ⁇ l of a serum sample is mixed with 50 ⁇ l of a solution of 10 mM bis-tris, 3.1 mM sodium azide, 0.05% Tween 20, 1 M HCl a_d pH 7.0 , 0.8 mM Tris base, 0.15 mM FeCl3, 0.15 M sodium citrate and 0.4 mM maleic acid.
- the chloride content of the medium is carefully adjusted to retain substantially all transferrin molecules with more than two sialic acid residues (this may be monitored by HPLC or isoelectric focusing) . Thereafter, 0.25 ml of a 25% suspension elderberry bark lectin (Vector Laboratories, US) is added (this ensures a more complete mopping up of sialylated transferrin molecules) , and the suspension is mixed gently. The suspension is thereafter filtered by centrifugation in a Millipore Ultra-Free UFC3 OHV filter cup, and the filtrate is collected.
- concentration of transferrin in the filtrate is determined by interpolating the nephelometric signal in a standard curve constructed from standards of known concentrations of human transferrin.
- 20 ⁇ l of a serum sample is mixed with 50 ⁇ l of a solution of 10/ mM bis-tris, 3.1 mM sodium azide, 0.05% Tween 20, 1 M HCl ad pH 7.0, 0.8 mM Tris base, 0.15 mM FeCl3, 0.15 M sodium citrate and 0.4 mM maleic acid.
- the chloride content of the medium is carefully adjusted to retain substantially all transferrin molecules with more than two sialic acid residues (this may be monitored by HPLC or isoelectric focusing) .
- the concentration of transferrin in the filtrate is determined by interpolating the nephelometric signal in a standard curve constructed from standards of known concentrations of human transferrin.
- Pipettes covering volumes from 4 ⁇ l to 3ml Alternatively: multipipettes for volumes lOO ⁇ l, 200 ⁇ l, 2ml and 3ml Racks (for tubes (75 x 12mm)
- the 0.3M Tris/PEG pH 7.4 comprises: 0.3m Tris. HCl
- transferrin content in the serum sample is calculated from the calibration curve.
- Figure 3 shows separation of transferrin isoforms by HPLC. The separation of monosialo and disialo is not complete, as can be seen between 9 and 10 min.
- Figures 4A and 4B show correlation of asialo vs monosialo, in A determined in % transferrin, in B determined in ⁇ g/mL.
- the squared correlation coefficient based on percentage determinations (Fig. 4A) was 0.5235.
- the squared correlation coefficient was 0.3339.
- the graphs are produced using data from the RIA method.
- Figures 5A and 5B show correlation of asialo vs disialo, in A determined in % transferrin, in B determined in ⁇ g/mL.
- the graphs are produced using data from teh RIA method.
- the squared correlation coefficient based on percentage determination (relative units) was 0.9501 (see Fig. 5a) . Based on mass units (Fig. 5B) the squared correlation coefficient was 0.8603.
- Figure 6 shows the correlation of (asialo-, monosialo- and disialo- transferrin) with asialo transferrin, determined in mass units ( ⁇ g/mL) .
- the squared correlation coefficient was 0.8797.
- the graph is produced using data from the RIA method.
- Figure 7 shows the correlation of (asialo-, monosialo- and disialo- transferrin) with disialotransferrin, determined in mass units ( ⁇ g/mL) .
- the squared correlation co-efficient was 0.9176.
- the graph is produced using data from the RIA method.
- Figure 8 shows the correlation of asialo transferrin with (monosialo- and disialo-) transferrin, determined in % transferrin. A reasonable correlation was found. The squared correlation coefficient was 0.8596. The graphs are produced using data from the RIA method.
- Figure 9 shows the correlation of asialo- with trisialo- transferrin, determined in % transferrin. As expected, no correlation was found. The squared correlation coefficient was very low, at 0.01754. The graph is produced using data from the RIA method.
- Figure 10 shows the correlation of (asialo-, monosialo- and disialo-transferrin) with asialotransferrin, determined in % transferrin.
- the squared correlation coefficient was 0.9278.
- the graph is produced using data from the RIA method.
- Figure 11 shows the correlation of (asialo-, monosialo- and disialo- transferrin) with disialotransferrin, determined in % transferrin.
- the squared correlation coefficient was 0.9906.
- the graph is produced using data from the RIA method.
- Example 9 illustrates that complete separation of the disialo transferrin is not required because the presence of the monosialo-variant in the determined or separated fraction is not harmful to the correlation results.
Abstract
Description
Claims
Priority Applications (8)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AT00981475T ATE283488T1 (en) | 1999-12-10 | 2000-12-11 | TRANSFERRIN ASSAY |
EP00981475A EP1247101B1 (en) | 1999-12-10 | 2000-12-11 | Transferrin assay |
CA002393556A CA2393556A1 (en) | 1999-12-10 | 2000-12-11 | Transferrin assay |
JP2001544033A JP2003516543A (en) | 1999-12-10 | 2000-12-11 | Assay |
AU18710/01A AU1871001A (en) | 1999-12-10 | 2000-12-11 | Assay |
DE60016281T DE60016281T2 (en) | 1999-12-10 | 2000-12-11 | TRANSFERRIN ASSAY |
DK00981475T DK1247101T3 (en) | 1999-12-10 | 2000-12-11 | Transferrin assay |
US10/167,983 US7166473B2 (en) | 1999-12-10 | 2002-06-10 | Transferrin assay |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US17024299P | 1999-12-10 | 1999-12-10 | |
GB9929308.6 | 1999-12-10 | ||
GBGB9929308.6A GB9929308D0 (en) | 1999-12-10 | 1999-12-10 | Assay |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US10/167,983 Continuation US7166473B2 (en) | 1999-12-10 | 2002-06-10 | Transferrin assay |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2001042795A2 true WO2001042795A2 (en) | 2001-06-14 |
WO2001042795A3 WO2001042795A3 (en) | 2002-05-10 |
Family
ID=10866134
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/GB2000/004732 WO2001042795A2 (en) | 1999-12-10 | 2000-12-11 | Transferrin assay |
Country Status (11)
Country | Link |
---|---|
US (1) | US7166473B2 (en) |
EP (1) | EP1247101B1 (en) |
JP (1) | JP2003516543A (en) |
AT (1) | ATE283488T1 (en) |
AU (1) | AU1871001A (en) |
CA (1) | CA2393556A1 (en) |
DE (1) | DE60016281T2 (en) |
DK (1) | DK1247101T3 (en) |
ES (1) | ES2233484T3 (en) |
GB (1) | GB9929308D0 (en) |
WO (1) | WO2001042795A2 (en) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU2002307776A1 (en) * | 2002-04-16 | 2003-10-27 | Kamada Ltd. | Ultrapure transferrin for pharmaceutical compositions |
US7691640B2 (en) * | 2005-09-30 | 2010-04-06 | Adeline Vanderver | Biochemical marker for diagnosing a leukodystrophy |
EP2440928A4 (en) * | 2009-06-08 | 2012-12-12 | Acrotech Systems Inc | Rapid detection of cerebrospinal fluid, methods and systems therefore |
WO2011052804A1 (en) * | 2009-10-30 | 2011-05-05 | Tokyo University Of Science Educational Foundation Administrative Organization | Method of delivering agent into target cell |
RU2461832C2 (en) * | 2010-07-02 | 2012-09-20 | Государственное образовательное учреждение Высшего профессионального образования "Омская государственная медицинская академия Федерального агентства по здравоохранению и социальному развитию Росздрава" | Diagnostic technique for alcohol abuse |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1996026444A1 (en) * | 1995-02-22 | 1996-08-29 | Axis Biochemicals Asa | Carbohydrate-deficient transferrin assay |
US5788845A (en) * | 1993-08-06 | 1998-08-04 | Biolin Medical Ab | Quantitation of carbohydrate deficient transferrin in high alcohol consumption by HPLC |
WO1999000672A1 (en) * | 1997-06-26 | 1999-01-07 | Axis-Shield Asa | Assay for carbohydrate-free transferrin |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SE440699B (en) * | 1984-02-06 | 1985-08-12 | Pharmacia Ab | ASSUME MEDIUM ISOTRANSFERRIN DETERMINATION ESTIMATE AN INDIVIDUAL ALCOHOL CONSUMPTION |
DK0535162T3 (en) * | 1990-06-21 | 1995-06-12 | Axis Biochemicals As | Analysis for analyte variants |
US5798212A (en) * | 1995-02-22 | 1998-08-25 | Axis Biochemicals Asa | CDT assay |
GB9827411D0 (en) * | 1998-12-11 | 1999-02-03 | Axis Biochemicals Asa | Dipstick assay |
-
1999
- 1999-12-10 GB GBGB9929308.6A patent/GB9929308D0/en not_active Ceased
-
2000
- 2000-12-11 EP EP00981475A patent/EP1247101B1/en not_active Expired - Lifetime
- 2000-12-11 JP JP2001544033A patent/JP2003516543A/en not_active Withdrawn
- 2000-12-11 AT AT00981475T patent/ATE283488T1/en not_active IP Right Cessation
- 2000-12-11 DE DE60016281T patent/DE60016281T2/en not_active Expired - Fee Related
- 2000-12-11 AU AU18710/01A patent/AU1871001A/en not_active Abandoned
- 2000-12-11 ES ES00981475T patent/ES2233484T3/en not_active Expired - Lifetime
- 2000-12-11 DK DK00981475T patent/DK1247101T3/en active
- 2000-12-11 CA CA002393556A patent/CA2393556A1/en not_active Abandoned
- 2000-12-11 WO PCT/GB2000/004732 patent/WO2001042795A2/en active IP Right Grant
-
2002
- 2002-06-10 US US10/167,983 patent/US7166473B2/en not_active Expired - Fee Related
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5788845A (en) * | 1993-08-06 | 1998-08-04 | Biolin Medical Ab | Quantitation of carbohydrate deficient transferrin in high alcohol consumption by HPLC |
WO1996026444A1 (en) * | 1995-02-22 | 1996-08-29 | Axis Biochemicals Asa | Carbohydrate-deficient transferrin assay |
WO1999000672A1 (en) * | 1997-06-26 | 1999-01-07 | Axis-Shield Asa | Assay for carbohydrate-free transferrin |
Also Published As
Publication number | Publication date |
---|---|
DE60016281D1 (en) | 2004-12-30 |
JP2003516543A (en) | 2003-05-13 |
US20030087450A1 (en) | 2003-05-08 |
DE60016281T2 (en) | 2005-12-22 |
CA2393556A1 (en) | 2001-06-14 |
GB9929308D0 (en) | 2000-02-02 |
US7166473B2 (en) | 2007-01-23 |
EP1247101A2 (en) | 2002-10-09 |
ATE283488T1 (en) | 2004-12-15 |
AU1871001A (en) | 2001-06-18 |
WO2001042795A3 (en) | 2002-05-10 |
ES2233484T3 (en) | 2005-06-16 |
DK1247101T3 (en) | 2005-03-29 |
EP1247101B1 (en) | 2004-11-24 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Salmela et al. | Carbohydrate‐deficient transferrin during 3 weeks' heavy alcohol consumption | |
EP1141714B1 (en) | Dipstick for carbohydrate-free transferrin assay | |
AU654497B2 (en) | Analyte variant analysis | |
US4624916A (en) | Process and composition for the rapid quantitation of small levels of creative kinase-MB isoenzyme | |
US20050239137A1 (en) | Assay for carbohydrate-free transferrin | |
US7166473B2 (en) | Transferrin assay | |
US6103478A (en) | CDT assay | |
US5798212A (en) | CDT assay | |
JP4753366B2 (en) | % CDT quantification method | |
AU5810294A (en) | Method and kit for the determination of antibodies | |
JP2003277398A (en) | Antibody against transferrin-including immune complex, method of producing the same, hybridoma and immunity measuring method |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
AK | Designated states |
Kind code of ref document: A2 Designated state(s): AE AG AL AM AT AT AU AZ BA BB BG BR BY BZ CA CH CN CR CU CZ CZ DE DE DK DK DM DZ EE EE ES FI FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NO NZ PL PT RO RU SD SE SG SI SK SK SL TJ TM TR TT TZ UA UG US UZ VN YU ZA ZW |
|
AL | Designated countries for regional patents |
Kind code of ref document: A2 Designated state(s): GH GM KE LS MW MZ SD SL SZ TZ UG ZW AM AZ BY KG KZ MD RU TJ TM AT BE CH CY DE DK ES FI FR GB GR IE IT LU MC NL PT SE TR BF BJ CF CG CI CM GA GN GW ML MR NE SN TD TG |
|
121 | Ep: the epo has been informed by wipo that ep was designated in this application | ||
DFPE | Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101) | ||
AK | Designated states |
Kind code of ref document: A3 Designated state(s): AE AG AL AM AT AT AU AZ BA BB BG BR BY BZ CA CH CN CR CU CZ CZ DE DE DK DK DM DZ EE EE ES FI FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NO NZ PL PT RO RU SD SE SG SI SK SK SL TJ TM TR TT TZ UA UG US UZ VN YU ZA ZW |
|
AL | Designated countries for regional patents |
Kind code of ref document: A3 Designated state(s): GH GM KE LS MW MZ SD SL SZ TZ UG ZW AM AZ BY KG KZ MD RU TJ TM AT BE CH CY DE DK ES FI FR GB GR IE IT LU MC NL PT SE TR BF BJ CF CG CI CM GA GN GW ML MR NE SN TD TG |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2393556 Country of ref document: CA |
|
ENP | Entry into the national phase |
Ref country code: JP Ref document number: 2001 544033 Kind code of ref document: A Format of ref document f/p: F |
|
WWE | Wipo information: entry into national phase |
Ref document number: 10167983 Country of ref document: US |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2000981475 Country of ref document: EP |
|
WWP | Wipo information: published in national office |
Ref document number: 2000981475 Country of ref document: EP |
|
REG | Reference to national code |
Ref country code: DE Ref legal event code: 8642 |
|
WWG | Wipo information: grant in national office |
Ref document number: 2000981475 Country of ref document: EP |