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WO1999029905B1 - Methode de detection de l'apoptose a l'aide d'oligonucleotides marques par fret - Google Patents

Methode de detection de l'apoptose a l'aide d'oligonucleotides marques par fret

Info

Publication number
WO1999029905B1
WO1999029905B1 PCT/US1998/026432 US9826432W WO9929905B1 WO 1999029905 B1 WO1999029905 B1 WO 1999029905B1 US 9826432 W US9826432 W US 9826432W WO 9929905 B1 WO9929905 B1 WO 9929905B1
Authority
WO
WIPO (PCT)
Prior art keywords
oligonucleotide
nucleotide sequence
moiety
detectable
energy
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.)
Ceased
Application number
PCT/US1998/026432
Other languages
English (en)
Other versions
WO1999029905A2 (fr
WO1999029905A3 (fr
Inventor
William M James
Irina A Nazarenko
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Serocor Inc
Original Assignee
Intergen Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Intergen Co filed Critical Intergen Co
Priority to EP98963108A priority Critical patent/EP1036201A2/fr
Priority to JP2000524476A priority patent/JP2001526052A/ja
Priority to CA002314225A priority patent/CA2314225A1/fr
Publication of WO1999029905A2 publication Critical patent/WO1999029905A2/fr
Publication of WO1999029905A3 publication Critical patent/WO1999029905A3/fr
Publication of WO1999029905B1 publication Critical patent/WO1999029905B1/fr
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12Q—MEASURING 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
    • C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
    • C12Q1/6813—Hybridisation assays
    • C12Q1/6816—Hybridisation assays characterised by the detection means
    • C12Q1/6818—Hybridisation assays characterised by the detection means involving interaction of two or more labels, e.g. resonant energy transfer
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12Q—MEASURING 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
    • C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
    • C12Q1/6844—Nucleic acid amplification reactions
    • C12Q1/6862—Ligase chain reaction [LCR]

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Zoology (AREA)
  • Wood Science & Technology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Health & Medical Sciences (AREA)
  • Biophysics (AREA)
  • General Engineering & Computer Science (AREA)
  • Immunology (AREA)
  • Microbiology (AREA)
  • Molecular Biology (AREA)
  • Analytical Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • Genetics & Genomics (AREA)
  • Biochemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Biotechnology (AREA)
  • General Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)

Abstract

L'invention concerne des méthodes d'amplification en chaîne par polymérase induite par ligase (LM-PCR) utilisées pour détecter des fragments cibles d'acides nucléiques à double brin tels que ceux qui sont générés lors du processus apoptosique. Selon ces méthodes, un oligonucléotide détectable est incorporé dans la cible. Cet oligonucléotide détectable renferme la fraction donneur et/ou la fraction receveur d'une paire de transfert d'énergie moléculaire (MET). Un exemple de paire MET est une paire de transfert par résonance d'énergie de fluorescence (FRET) constituée d'une fraction fluorophore (donneur) et d'une fraction extinctrice de luminescence (receveur). La fraction donneur de la paire MET émet de l'énergie détectable telle que de la lumière seulement lorsque l'oligonucléotide détectable est incorporé dans la cible. Selon ces méthodes, un oligonucléotide lieur-amorce est attaché à un oligonucléotide d'aide à la liaison, ou un oligonucléotide lieur-amorce renfermant une séquence d'aide à la liaison est lié à l'extrémité 5' de chacun des brins d'un fragment d'acides nucléiques à double brin renfermant soit une extrémité franche soit un surplomb terminal. Après cette étape de liaison, un oligonucléotide détectable capable d'être attaché au complément de l'oligonuléotide lieur-amorce est incorporé dans la cible par réactions catalysées par polymérase. Selon un autre mode de réalisation, l'oligonucléotide lieur-amorce est également un oligonucléotide détectable. Eventuellement, la cible marquée par l'oligonucléotide détectable est ensuite amplifiée, l'oligonucléotide détectable étant incorporé au produit d'amplification. La cible est détectée par détection de l'énergie émise par le groupe donneur de l'oligonucléotide détectable.
PCT/US1998/026432 1997-12-12 1998-12-11 Methode de detection de l'apoptose a l'aide d'oligonucleotides marques par fret Ceased WO1999029905A2 (fr)

Priority Applications (3)

Application Number Priority Date Filing Date Title
EP98963108A EP1036201A2 (fr) 1997-12-12 1998-12-11 Methode de detection de l'apoptose a l'aide d'oligonucleotides marques par fret
JP2000524476A JP2001526052A (ja) 1997-12-12 1998-12-11 Ｆｒｅｔ標識オリゴヌクレオチドを用いたアポトーシスを検出する方法
CA002314225A CA2314225A1 (fr) 1997-12-12 1998-12-11 Methode de detection de l'apoptose a l'aide d'oligonucleotides marques par fret

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US6943497P 1997-12-12 1997-12-12
US60/069,434 1997-12-12

Publications (3)

Publication Number Publication Date
WO1999029905A2 WO1999029905A2 (fr) 1999-06-17
WO1999029905A3 WO1999029905A3 (fr) 1999-08-26
WO1999029905B1 true WO1999029905B1 (fr) 1999-10-21

Family

ID=22088952

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US1998/026432 Ceased WO1999029905A2 (fr) 1997-12-12 1998-12-11 Methode de detection de l'apoptose a l'aide d'oligonucleotides marques par fret

Country Status (4)

Country Link
EP (1) EP1036201A2 (fr)
JP (1) JP2001526052A (fr)
CA (1) CA2314225A1 (fr)
WO (1) WO1999029905A2 (fr)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE10048009A1 (de) * 2000-09-26 2002-04-11 Cytonet Gmbh & Co Kg Verfahren zum Nachweis von Pilzinfektionen
CA2426812A1 (fr) * 2000-10-24 2002-05-02 Intergen Company Detection de sequences nucleotidiques specifiques
CN1556224B (zh) * 2004-01-08 2012-08-22 湖南大学 核酸片段检测系统及其在核酸分析及相关酶研究中的应用
EP3260556B1 (fr) 2006-05-31 2019-07-31 Sequenom, Inc. Procédés pour l'extraction d'acide nucléique à partir d'un échantillon
WO2010115016A2 (fr) 2009-04-03 2010-10-07 Sequenom, Inc. Compositions constituées d'une préparation d'acides nucléiques et procédés associés
US9957393B2 (en) 2015-03-30 2018-05-01 Enzo Biochem, Inc. Monoazo dyes with cyclic amine as fluorescence quenchers
CN109182479A (zh) * 2018-07-27 2019-01-11 广州医科大学附属第医院 一种实时荧光定量pcr通用型荧光探针及其应用

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5843658A (en) * 1995-03-10 1998-12-01 Hamamatsu Photonics K.K. Method of measuring oligonucleotide decomposing activity
DK0843725T3 (da) * 1995-08-11 2002-08-12 Novozymes As Fremgangmåde til fremstilling af polypeptidvarianter
CA2240667A1 (fr) * 1995-12-18 1997-06-26 Washington University Procede d'analyse d'acide nucleique par transfert des energies de resonance par fluorescence
CA2252048C (fr) * 1996-04-12 2008-03-11 The Public Health Research Institute Of The City Of New York, Inc. Sondes, trousses et dosages de detection
US6117635A (en) * 1996-07-16 2000-09-12 Intergen Company Nucleic acid amplification oligonucleotides with molecular energy transfer labels and methods based thereon

Also Published As

Publication number Publication date
CA2314225A1 (fr) 1999-06-17
WO1999029905A2 (fr) 1999-06-17
JP2001526052A (ja) 2001-12-18
EP1036201A2 (fr) 2000-09-20
WO1999029905A3 (fr) 1999-08-26

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