JP2005502882A5 - - Google Patents

Download PDF

Info

Publication number
JP2005502882A5
JP2005502882A5 JP2003527426A JP2003527426A JP2005502882A5 JP 2005502882 A5 JP2005502882 A5 JP 2005502882A5 JP 2003527426 A JP2003527426 A JP 2003527426A JP 2003527426 A JP2003527426 A JP 2003527426A JP 2005502882 A5 JP2005502882 A5 JP 2005502882A5
Authority
JP
Japan
Prior art keywords
polypeptide
tse
molecular weight
body fluid
sample
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP2003527426A
Other languages
Japanese (ja)
Other versions
JP4312049B2 (en
JP2005502882A (en
Filing date
Publication date
Priority claimed from GB0121459A external-priority patent/GB2379737A/en
Application filed filed Critical
Publication of JP2005502882A publication Critical patent/JP2005502882A/en
Publication of JP2005502882A5 publication Critical patent/JP2005502882A5/ja
Application granted granted Critical
Publication of JP4312049B2 publication Critical patent/JP4312049B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Claims (23)

感染性海綿状脳症(TSE)または該TSEを患っている疑いのある被験者においてその可能性の診断方法は、
前記被験者から取り出した体液のサンプルを質量分析にかけて、それにより該サンプルにおけるポリペプチドのテスト量を決定し、
前記テスト量が前記TSEの診断に対応するか否かを判断することを備え、
前記ポリペプチドは、TSE感染被験者と非感染被験者の前記体液で相違して含まれており、約4780、約6700、約8600、約13375、約3970、約3990、約4294、約4478、約10075、約11730、約14043、約17839、約7700、約3295、約4315、約4436、約6200、約8936、約9107、約9145、約9185、約9454、約13550、約7574、約7930、約7975、約8020、または約10220Daの分子量を有する。
Infectious spongiform encephalopathy (TSE) or a method of diagnosing that possibility in a subject suspected of suffering from the TSE is:
Subjecting a sample of body fluid removed from the subject to mass spectrometry, thereby determining a test amount of the polypeptide in the sample;
Determining whether the test quantity corresponds to a diagnosis of the TSE;
The polypeptide is contained differently in the body fluids of TSE infected and non-infected subjects and is about 4780, about 6700, about 8600, about 13375, about 3970, about 3990, about 4294, about 4478, about 10075. , About 11730, about 14043, about 17839, about 7700, about 3295, about 4315, about 4436, about 6200, about 8936, about 9107, about 9145, about 9185, about 9454, about 13550, about 7574, about 7930, about It has a molecular weight of 7975, about 8020, or about 10220 Da.
前記ポリペプチドは、TSE感染被験者の体液に存在し、非TSE感染被験者の体液には存在せず、これにより体液サンプル中の前記ポリペプチドの存在がTSEであることを示す請求項1に記載の方法。   2. The polypeptide of claim 1, wherein the polypeptide is present in the body fluid of a TSE infected subject and not in the body fluid of a non-TSE infected subject, thereby indicating that the presence of the polypeptide in a body fluid sample is TSE. Method. 前記ポリペプチドは、TSE感染被験者の体液に存在せず、非TSE感染被験者の体液には存在し、これにより体液サンプル中の前記ポリペプチドの非存在がTSEであることを示す請求項1に記載の方法。   2. The polypeptide is not present in the body fluid of a TSE-infected subject but is present in the body fluid of a non-TSE-infected subject, thereby indicating that the absence of the polypeptide in the body fluid sample is TSE. the method of. 前記質量分析は、レーザー脱離/イオン化質量分析である請求項1から3のうちいずれか1項に記載の方法。   The method according to claim 1, wherein the mass spectrometry is laser desorption / ionization mass spectrometry. 前記サンプルは、固定化金属親和性捕獲(IMAC)、該ポリペプチドと結合する疎水性、強アニオン性、または弱カチオン性交換表面を有するプロープで吸収される請求項1から4のうちいずれか1項に記載の方法。   5. The sample of claim 1, wherein the sample is absorbed with a probe having immobilized metal affinity capture (IMAC), a hydrophobic, strong anionic, or weakly cationic exchange surface that binds to the polypeptide. The method according to item. 前記ポリペプチドは、表面増幅レーザー脱離/イオン化(SELDI)及び飛行時間型質量分析法(TOF−MS)によって決定される請求項1から5のうちいずれか1項に記載の方法。   6. The method of any one of claims 1-5, wherein the polypeptide is determined by surface amplified laser desorption / ionization (SELDI) and time-of-flight mass spectrometry (TOF-MS). 前記体液は、脳脊髄液、血漿、血清、血液、または涙である請求項1から6のうちいずれか1項に記載の方法。   The method according to any one of claims 1 to 6, wherein the body fluid is cerebrospinal fluid, plasma, serum, blood, or tears. 複数の前記ポリペプチドは前記サンプル内で決定される請求項1から7のうちいずれか1項に記載の方法。   8. The method of any one of claims 1 to 7, wherein a plurality of the polypeptides are determined within the sample. 前記TSEは、クロイツフェルト・ヤコブ病(CJD)である請求項1から8のうちいずれか1項に記載の方法。   The method according to any one of claims 1 to 8, wherein the TSE is Creutzfeldt-Jakob disease (CJD). 約4780、約6700、約8600、または約13375の分子量を有する1またはそれより多くのそれぞれのポリペプチドが決定され、そのようなポリペプチドの1つまたはそれより多い存在がCJDであることを示す請求項9に記載の方法。   One or more respective polypeptides having a molecular weight of about 4780, about 6700, about 8600, or about 13375 are determined, indicating that the presence of one or more of such polypeptides is CJD The method of claim 9. 約3970、約3990、約4294、約4478、約10075、約11730、約14043、または約17839の分子量をそれぞれ有する1つまたはそれより多いポリペプチドが決定され、そのようなポリペプチドの1つまたはそれより多い不存在がCJDを示す請求項9、または10に記載の方法。   One or more polypeptides each having a molecular weight of about 3970, about 3990, about 4294, about 4478, about 10075, about 11730, about 14043, or about 17839 are determined, and one or more of such polypeptides 11. A method according to claim 9 or 10, wherein a greater absence indicates CJD. 約7700の分子量を有するポリペプチドが決定され、そのようなポリペプチドの存在がCJDであることを示す請求項9から11のうちいずれか1項に記載の方法。   12. A method according to any one of claims 9 to 11 wherein a polypeptide having a molecular weight of about 7700 is determined and the presence of such a polypeptide is CJD. 約3295、約4315、約4436、約6200、約8936、約9107、約9145、約9185、約9454、または約13550Daの分子量を有するポリペプチドが決定され、そのようなポリペプチドの1つ以上の不存在または減少量がCJDであることを示す請求項9から12のうちいずれか1項に記載の方法。   A polypeptide having a molecular weight of about 3295, about 4315, about 4436, about 6200, about 8936, about 9107, about 9145, about 9185, about 9454, or about 13550 Da is determined, and one or more of such polypeptides 13. A method according to any one of claims 9 to 12, wherein the absence or reduction amount indicates CJD. 約7574、約7930、約7975、または約8020Daの分子量を有するポリペプチドが決定され、そのようなポリペプチドの1つ以上の存在または増加量がCJDであることを示す請求項9から13のうちいずれか1項に記載の方法。   The polypeptide of claim 9 to 13, wherein a polypeptide having a molecular weight of about 7574, about 7930, about 7975, or about 8020 Da is determined and indicates that the presence or increase of one or more of such polypeptides is CJD The method according to any one of the above. 前記TSEは牛海綿状脳症(BSE)である請求項1から8のうちいずれか1項に記載の方法。   9. The method according to any one of claims 1 to 8, wherein the TSE is bovine spongiform encephalopathy (BSE). 前記ポリペプチドは約10220の分子量を有し、該ポリペプチドの存在がBSEであることを示す請求項15に記載の方法。   16. The method of claim 15, wherein the polypeptide has a molecular weight of about 10220, wherein the presence of the polypeptide is BSE. 前記TSEはスクレピーである請求項1から8のうちいずれか1項に記載の方法。   9. A method according to any one of claims 1 to 8, wherein the TSE is scrapie. 診断、前兆、治療への適用に対して、TSE感染被験者と非感染被験者の体液で相違して含まれるポリペプチドの使用であって、
前記ポリペプチドは、約4780、約6700、約8600、約13375、約3970、約3990、約4294、約4478、約10075、約11730、約14043、約17839、約7700、約3295、約4315、約4436、約6200、約8936、約9107、約9145、約9185、約9454、約13550、約7574、約7930、約7975、約8020、または約10220Daの分子量を有し、質量分析により決定することができる。
Use of a polypeptide that is differentially contained in the body fluids of a TSE-infected subject and a non-infected subject for diagnostic, predictive, therapeutic applications,
The polypeptide comprises about 4780, about 6700, about 8600, about 13375, about 3970, about 3990, about 4294, about 4478, about 10075, about 11730, about 14043, about 17839, about 7700, about 3295, about 4315, Having a molecular weight of about 4436, about 6200, about 8936, about 9107, about 9145, about 9185, about 9454, about 13550, about 7574, about 7930, about 7975, about 8020, or about 10220 Da, determined by mass spectrometry be able to.
診断、前兆、治療への適用に対しての材料の使用であって、
該材料は、TSE感染被験者と非感染被験者の体液で相違して含まれるポリペプチドを認識したり、該ポリペプチドと結合したり、または該ポリペプチドと親和性を有したりし、
前ポリペプチドは、約4780、約6700、約8600、約13375、約3970、約3990、約4294、約4478、約10075、約11730、約14043、約17839、約7700、約3295、約4315、約4436、約6200、約8936、約9107、約9145、約9185、約9454、約13550、約7574、約7930、約7975、約8020、または約10220Daの分子量を有し、質量分析により決定することができる。
The use of materials for diagnostic, predictive, therapeutic applications,
The material recognizes a polypeptide contained differently in the body fluid of a TSE-infected subject and a non-infected subject, binds to the polypeptide, or has an affinity for the polypeptide,
The pre-polypeptide is about 4780, about 6700, about 8600, about 13375, about 3970, about 3990, about 4294, about 4478, about 10075, about 11730, about 14043, about 17839, about 7700, about 3295, about 4315, Having a molecular weight of about 4436, about 6200, about 8936, about 9107, about 9145, about 9185, about 9454, about 13550, about 7574, about 7930, about 7975, about 8020, or about 10220 Da, determined by mass spectrometry be able to.
前記材料は、抗体または抗体チップである請求項19に記載の使用。   The use according to claim 19, wherein the material is an antibody or an antibody chip. TSEの診断で使用するためのキットであって、体液のサンプルを受け取って、質量分析で配置するためのプローブからなり、
それにより該サンプルでのポリペプチドのテスト量を決定し、
該ポリペプチドはTSE感染被験者とTSE非感染の被験者との体液で相違して含まれており、
該ポリペプチドは、約4780、約6700、約8600、約13375、約3970、約3990、約4294、約4478、約10075、約11730、約14043、約17839、約7700、約3295、約4315、約4436、約6200、約8936、約9107、約9145、約9185、約9454、約13550、約7574、約7930、約7975、約8020、または約10220Daの分子量を有する。
A kit for use in diagnosis of TSE comprising a probe for receiving a sample of body fluid and placing it in mass spectrometry;
Thereby determining the test amount of polypeptide in the sample,
The polypeptide is contained differently in body fluids between TSE-infected subjects and non-TSE-infected subjects,
The polypeptide is about 4780, about 6700, about 8600, about 13375, about 3970, about 3990, about 4294, about 4478, about 10075, about 11730, about 14043, about 17839, about 7700, about 3295, about 4315, It has a molecular weight of about 4436, about 6200, about 8936, about 9107, about 9145, about 9185, about 9454, about 13550, about 7574, about 7930, about 7975, about 8020, or about 10220 Da.
前記プローブは前記ポリペプチドの吸収のための吸着剤を含む請求項21に記載のキット。   The kit of claim 21, wherein the probe comprises an adsorbent for absorption of the polypeptide. さらに、前記プローブから非結合または弱い結合の前記材料を取り除くための洗浄溶液を備える請求項22に記載のキット。   23. The kit of claim 22, further comprising a wash solution for removing unbound or weakly bound material from the probe.
JP2003527426A 2001-09-05 2002-09-03 Test method for use in the diagnosis of infectious spongiform encephalopathy Expired - Fee Related JP4312049B2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB0121459A GB2379737A (en) 2001-09-05 2001-09-05 Diagnostic method for spongiform encephalopathy disease
PCT/EP2002/010063 WO2003023406A2 (en) 2001-09-05 2002-09-03 Diagnostic method for transmissible spongiform encephalopathies

Publications (3)

Publication Number Publication Date
JP2005502882A JP2005502882A (en) 2005-01-27
JP2005502882A5 true JP2005502882A5 (en) 2005-11-17
JP4312049B2 JP4312049B2 (en) 2009-08-12

Family

ID=9921541

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2003527426A Expired - Fee Related JP4312049B2 (en) 2001-09-05 2002-09-03 Test method for use in the diagnosis of infectious spongiform encephalopathy

Country Status (6)

Country Link
EP (1) EP1423703A2 (en)
JP (1) JP4312049B2 (en)
AU (1) AU2002331112B2 (en)
CA (1) CA2459500A1 (en)
GB (1) GB2379737A (en)
WO (1) WO2003023406A2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1556702A2 (en) * 2002-10-30 2005-07-27 Proteome Sciences Plc Diagnostic methods for transmissible spongiform encephalopathies (prion diseases)

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1998026293A1 (en) * 1996-12-12 1998-06-18 Neuromark Methods of detecting transmissible spongiform encephalopathies by detecting 14-3-3 protein isoforms
NZ516848A (en) * 1997-06-20 2004-03-26 Ciphergen Biosystems Inc Retentate chromatography apparatus with applications in biology and medicine
DE19918141A1 (en) * 1999-04-21 2000-10-26 Boehringer Ingelheim Vetmed Diagnosing transmissible spongiform encephalopathy, particularly before appearance of clinical symptoms, by detecting specific markers in blood cells
DE19923811C1 (en) * 1999-05-20 2000-12-07 Robert Koch Inst Procedure for the diagnosis of TSE-induced changes in tissues using infrared spectroscopy
NZ516240A (en) * 1999-06-23 2005-11-25 Caprion Pharmaceuticals Inc Prion protein peptides and uses thereof
ATE350662T1 (en) * 1999-10-07 2007-01-15 Ciphergen Biosystems Inc MARKER PROTEINS FOR PROSTATE CANCER
GB2360089A (en) * 2000-03-10 2001-09-12 Univ Geneve Diagnostic assay for transmisible spongiform encephalopathies

Similar Documents

Publication Publication Date Title
EP1802322A2 (en) Prion protein binding materials and methods of use
Bros et al. Quantitative detection of amyloid-β peptides by mass spectrometry: state of the art and clinical applications
JPWO2008065806A1 (en) Mass spectrometry of biological samples using immunoprecipitation
Kim et al. Direct Monitoring of Fucosylated Glycopeptides of Alpha‐Fetoprotein in Human Serum for Early Hepatocellular Carcinoma by Liquid Chromatography–Tandem Mass Spectrometry with Immunoprecipitation
EP2764368A1 (en) METHOD FOR DETECTING Aß-SPECIFIC ANTIBODIES IN A BIOLOGICAL SAMPLE
Albertini et al. Optimization protocol for amyloid‐β peptides detection in human cerebrospinal fluid using SELDI TOF MS
Steinacker et al. Ubiquitin as potential cerebrospinal fluid marker of Creutzfeldt–Jakob disease
JP5322556B2 (en) Novel nonalcoholic fatty liver disease biomarker and method for detecting nonalcoholic fatty liver disease using the biomarker
JP2012108160A (en) β-2 MICROGLOBULIN AS BIOMARKERS FOR PERIPHERAL ARTERIAL DISEASE
JP2005502882A5 (en)
JP2006514284A5 (en)
US20210405061A1 (en) Method for measuring ab peptide
JP2004529314A (en) How to determine prion strains
Schneck et al. Current trends in magnetic particle enrichment for mass spectrometry-based analysis of cardiovascular protein biomarkers
Jiayu et al. A rapid method for detection of PrP by surface plasmon resonance (SPR)
Za'abi et al. Analyses of acute kidney injury biomarkers by ultra‐high performance liquid chromatography with mass spectrometry
Ishida et al. Activation of complement system in adult T-cell leukemia (ATL) occurs mainly through lectin pathway: a serum proteomic approach using mass spectrometry
Wu et al. Detection of Dengue Fever Nonstructural Protein 1 Antigen by Proteolytic Peptide Imprinting Technology and UHPLC–MS/MS
JP7478040B2 (en) METHOD FOR MEASURING Aβ PEPTIDE AND REAGENT COMPOSITION USED IN THE METHOD
Shah et al. Developing an iMALDI method
Varshney et al. Prion protein detection in serum using micromechanical resonator arrays
Kim et al. Measuring fucosylated alpha‐fetoprotein in hepatocellular carcinoma: A comparison of μTAS and parallel reaction monitoring
US20200319208A1 (en) Method for quantifying protein aggregates of a protein misfolding disease in a sample
JP4312049B2 (en) Test method for use in the diagnosis of infectious spongiform encephalopathy
EP2570421A1 (en) Method to purify and concentrate prions from complex mixtures such as plasma into a target solution