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WO2009011426A1 - γ-セクレターゼの新規基質c-Metを利用したスクリーニング方法 - Google Patents

γ-セクレターゼの新規基質c-Metを利用したスクリーニング方法 Download PDF

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Publication number
WO2009011426A1
WO2009011426A1 PCT/JP2008/063037 JP2008063037W WO2009011426A1 WO 2009011426 A1 WO2009011426 A1 WO 2009011426A1 JP 2008063037 W JP2008063037 W JP 2008063037W WO 2009011426 A1 WO2009011426 A1 WO 2009011426A1
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Prior art keywords
met
secretase
screening method
method utilizing
novel substrate
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Ceased
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PCT/JP2008/063037
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English (en)
French (fr)
Inventor
Eiji Inoue
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Eisai R&D Management Co Ltd
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Eisai R&D Management Co Ltd
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Application filed by Eisai R&D Management Co Ltd filed Critical Eisai R&D Management Co Ltd
Priority to JP2009523688A priority Critical patent/JPWO2009011426A1/ja
Priority to EP08791346A priority patent/EP2177623A4/en
Publication of WO2009011426A1 publication Critical patent/WO2009011426A1/ja
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12QMEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q1/00Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/34Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving hydrolase
    • C12Q1/37Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving hydrolase involving peptidase or proteinase
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/74Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving hormones or other non-cytokine intercellular protein regulatory factors such as growth factors, including receptors to hormones and growth factors
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N2333/00Assays involving biological materials from specific organisms or of a specific nature
    • G01N2333/435Assays involving biological materials from specific organisms or of a specific nature from animals; from humans
    • G01N2333/705Assays involving receptors, cell surface antigens or cell surface determinants
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N2333/00Assays involving biological materials from specific organisms or of a specific nature
    • G01N2333/90Enzymes; Proenzymes
    • G01N2333/914Hydrolases (3)
    • G01N2333/948Hydrolases (3) acting on peptide bonds (3.4)
    • G01N2333/95Proteinases, i.e. endopeptidases (3.4.21-3.4.99)
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N2500/00Screening for compounds of potential therapeutic value
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N2500/00Screening for compounds of potential therapeutic value
    • G01N2500/02Screening involving studying the effect of compounds C on the interaction between interacting molecules A and B (e.g. A = enzyme and B = substrate for A, or A = receptor and B = ligand for the receptor)

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  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Molecular Biology (AREA)
  • Organic Chemistry (AREA)
  • Immunology (AREA)
  • Urology & Nephrology (AREA)
  • Biotechnology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Microbiology (AREA)
  • Physics & Mathematics (AREA)
  • Analytical Chemistry (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Biochemistry (AREA)
  • Hematology (AREA)
  • Biomedical Technology (AREA)
  • General Health & Medical Sciences (AREA)
  • Endocrinology (AREA)
  • Medicinal Chemistry (AREA)
  • General Engineering & Computer Science (AREA)
  • Cell Biology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Biophysics (AREA)
  • Food Science & Technology (AREA)
  • Genetics & Genomics (AREA)
  • General Physics & Mathematics (AREA)
  • Pathology (AREA)
  • Enzymes And Modification Thereof (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)
  • Investigating Or Analysing Biological Materials (AREA)

Abstract

 本発明は、γ-セクレターゼによるc-Metのプロセシングに影響を与える化合物をスクリーニングする方法であって、以下のステップ:   (i)候補化合物の存在下および非存在下で、γ-セクレターゼまたはその生物学的に活性な断片を含む第1の生物学的組成物と、c-Metを含む第2の生物学的組成物とを接触させ;   (ii)当該候補化合物の存在下および非存在下における当該c-Metの開裂をそれぞれ測定し;   (iii)γ-セクレターゼによる当該c-Metの開裂に影響を与える候補化合物を選択し;そして   (iv)前記(iii)で得られた候補化合物を、γ-セクレターゼによるc-Metのプロセシングに影響を与える化合物であると同定する、 ことを含む、上記方法。
PCT/JP2008/063037 2007-07-19 2008-07-18 γ-セクレターゼの新規基質c-Metを利用したスクリーニング方法 Ceased WO2009011426A1 (ja)

Priority Applications (2)

Application Number Priority Date Filing Date Title
JP2009523688A JPWO2009011426A1 (ja) 2007-07-19 2008-07-18 γ−セクレターゼの新規基質c−Metを利用したスクリーニング方法
EP08791346A EP2177623A4 (en) 2007-07-19 2008-07-18 SCREENING METHOD USING C-MET, A NEW SUBSTRATE FOR GAMMA SECRETASE

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US95062107P 2007-07-19 2007-07-19
US60/950,621 2007-07-19
US95149307P 2007-07-24 2007-07-24
US60/951,493 2007-07-24

Publications (1)

Publication Number Publication Date
WO2009011426A1 true WO2009011426A1 (ja) 2009-01-22

Family

ID=40259752

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP2008/063037 Ceased WO2009011426A1 (ja) 2007-07-19 2008-07-18 γ-セクレターゼの新規基質c-Metを利用したスクリーニング方法

Country Status (4)

Country Link
US (1) US20090191580A1 (ja)
EP (1) EP2177623A4 (ja)
JP (1) JPWO2009011426A1 (ja)
WO (1) WO2009011426A1 (ja)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2166110B1 (en) * 2007-06-08 2012-02-22 Eisai R&D Management Co., Ltd. Screening method utilizing novel substrate epha4 for gamma-secretase
JPWO2009017234A1 (ja) * 2007-08-01 2010-10-28 エーザイ・アール・アンド・ディー・マネジメント株式会社 γ−セクレターゼの新規基質c−Retを利用したスクリーニング方法
US8530181B2 (en) * 2007-11-15 2013-09-10 Eisai R&D Management Co., Ltd. Method of screening for compounds which affect the cleavage of EphA7 byγ-secretase
DK2223999T3 (en) * 2007-11-30 2017-12-18 Eisai R&D Man Co Ltd EPHA4 POLYPEPTIDE WITH UNKNOWN ACTIVITY AND USE THEREOF
BR112013010687A2 (pt) 2010-11-03 2016-08-02 Argen X Bv combinações de anticorpos c-met
US8865426B2 (en) 2010-12-17 2014-10-21 Eisai R&D Management Co., Ltd. Screening method using gelatinase-mediated EphA4 cleavage reaction as an indicator
JP5961608B2 (ja) 2011-04-25 2016-08-02 エーザイ・アール・アンド・ディー・マネジメント株式会社 EphA4細胞外ドメインの測定による認知機能障害を伴う神経系疾患の検出方法
AR119303A1 (es) 2019-07-01 2021-12-09 Eisai R&D Man Co Ltd Anticuerpo anti-epha4 humano

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US20020068361A1 (en) * 1997-04-08 2002-06-06 Douglas Clary Methods of evaluating specific cellular functions of receptor protein tyrosine kinases in a ligand independent manner
US20070026409A1 (en) * 2001-08-14 2007-02-01 The General Hospital Corporation Nucleic acid and amino acid sequences involved in pain
US20060241074A1 (en) * 2001-08-14 2006-10-26 The General Hospital Corporation Methods for treatment of pain
EP1478772A2 (en) * 2001-08-14 2004-11-24 The General Hospital Corporation Nucleic acid and amino acid sequences involved in pain
JP2004000060A (ja) * 2002-05-31 2004-01-08 Otsuka Pharmaceut Co Ltd アミロイドβ産生に影響を与える化合物のスクリーニング方法
EP1662259A1 (en) * 2004-11-25 2006-05-31 Cellzome Ag Use of Eph receptor inhibitors for the treatment of neurodegenerative diseases
EP1947193A1 (en) * 2007-01-17 2008-07-23 Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V. Screening method for anti-diabetic compounds
EP2166110B1 (en) * 2007-06-08 2012-02-22 Eisai R&D Management Co., Ltd. Screening method utilizing novel substrate epha4 for gamma-secretase
US20090023158A1 (en) * 2007-07-13 2009-01-22 Elan Pharmaceuticals, Inc. Compositions and Methods for Identifying Substrate Specificity of Inhibitors of Gamma Secretase
JPWO2009017234A1 (ja) * 2007-08-01 2010-10-28 エーザイ・アール・アンド・ディー・マネジメント株式会社 γ−セクレターゼの新規基質c−Retを利用したスクリーニング方法
US20090163594A1 (en) * 2007-10-31 2009-06-25 Elan Pharmaceuticals, Inc. Triple Assay System for Identifying Substrate Selectivity of Gamma Secretase Inhibitors
US8530181B2 (en) * 2007-11-15 2013-09-10 Eisai R&D Management Co., Ltd. Method of screening for compounds which affect the cleavage of EphA7 byγ-secretase
DK2223999T3 (en) * 2007-11-30 2017-12-18 Eisai R&D Man Co Ltd EPHA4 POLYPEPTIDE WITH UNKNOWN ACTIVITY AND USE THEREOF
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GEORGAKOPOULOS A. ET AL.: "Metalloproteinase/Presenilin1 processing of ephrinB regulates EphB-induced Src phosphorylation and signaling", EMBO J., vol. 25, March 2006 (2006-03-01), pages 1242 - 1252, XP008129422 *
KOPAN R. ET AL.: "Gamma-secretase: proteasome of the membrane?", NAT. REV. MOL. CELL BIOL., vol. 5, June 2004 (2004-06-01), pages 499 - 504, XP008061885 *
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See also references of EP2177623A4
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Also Published As

Publication number Publication date
US20090191580A1 (en) 2009-07-30
JPWO2009011426A1 (ja) 2010-09-24
EP2177623A4 (en) 2010-12-29
EP2177623A1 (en) 2010-04-21

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