CA2390312A1 - Oligomer array with pna and/or dna oligomers on a surface - Google Patents

Oligomer array with pna and/or dna oligomers on a surface Download PDF

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Publication number
CA2390312A1
CA2390312A1 CA002390312A CA2390312A CA2390312A1 CA 2390312 A1 CA2390312 A1 CA 2390312A1 CA 002390312 A CA002390312 A CA 002390312A CA 2390312 A CA2390312 A CA 2390312A CA 2390312 A1 CA2390312 A1 CA 2390312A1
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Canada
Prior art keywords
general formula
oligomers
oligomer
array according
sequence
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CA002390312A
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French (fr)
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CA2390312C (en
Inventor
Kurt Berlin
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Epigenomics AG
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Epigenomics Ag
Kurt Berlin
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Publication date
Application filed by Epigenomics Ag, Kurt Berlin filed Critical Epigenomics Ag
Publication of CA2390312A1 publication Critical patent/CA2390312A1/en
Application granted granted Critical
Publication of CA2390312C publication Critical patent/CA2390312C/en
Anticipated expiration legal-status Critical
Expired - Fee Related 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
    • C12Q1/68Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
    • C12Q1/6813Hybridisation assays
    • C12Q1/6827Hybridisation assays for detection of mutation or polymorphism
    • 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
    • C12Q1/68Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
    • C12Q1/6813Hybridisation assays
    • C12Q1/6834Enzymatic or biochemical coupling of nucleic acids to a solid phase
    • C12Q1/6837Enzymatic or biochemical coupling of nucleic acids to a solid phase using probe arrays or probe chips

Abstract

The invention relates to an oligomer array with PNA (Peptide Nucleic Acid) and/or DNA oligomers on a surface, said oligomers comprising oligomers of 6 to 20 monomers or nucleobases each. Said monomers or nucleobases comprise at least one sequence of the general formula DDCGDD or of the general formula DDTGDD or of the general formula HHCGHH or of the general formula HHCAHH, wherein H represents any of the bases adenine (A), cytosine (C) or thymine (T) and D represents any of the bases adenine (A), guanine (G) or thymine (T). The location of the oligomers on the surface is correlated with the sequence of the oligomers. The inventive oligomer arrays are used to detect cytosine methylations in genomic DNA.

Claims (11)

1. An oligomer array with PNA (peptide nucleic acids) and/or DNA oligomers on a surface, each comprising oligomers of between 6 and 20 monomers or nucleobases, whereby the latter each contain at least one sequence of the general formula DDCGDD or of the general formula DDTGDD or of the general formula HHCGHH or of the general formula HHCAHH, wherein H indicates one of the bases: adenine (A), cytosine (C), or thymine (T) and D represents one of the bases: adenine (A), guanine (G) or thymine (T), and wherein the site of the oligomers on the surface is correlated with the sequence of the oligomers, characterized in that at least 75% of the oligonudeotides contain a sequence of the general formula DDCGDD or of the general formula DDTGDD or of the general formula HHCGHH or of the general formula HHCAHH and that, fitted to each oligomer, which contains a CG sequence, an analogous oligomer is immobilized, which differs from said [first] oligomer only by the fact that it contains a TG
or a CA sequence instead of the CG sequence.
2. The oligomer array according to claim 1, further characterized in that the surface is planar and the oligomers are arranged thereon in a rectangular or hexagonal grid, which permits assignment to coordinates.
3. The oligomer array according to one of the preceding claims, comprising sequences of the general formula DDCGDD and of the general formula DDTGDD and of the general formula HHCGHH and of the general formula HHCAHH.
4. The oligomer array according to one of claims 1 to 2, comprising sequences of the general formula DDCGDD and of the general formula DDTGDD or sequences of the general formula HHCGHH and of the general formula HHCAHH.
5. The oligomer array according to one of the preceding claims, further characterized in that it comprises at least 100 different oligomers.
6. The oligomer array according to one of the preceding claims, further characterized in that the surface is [made] of glass.
7. The oligomer array according to one of claims 1 to 5, further characterized in that the surface is [made] of metal or another conductive material.
8. The oligomer array according to claim 7, further characterized in that the surface is the target of a MALDI mass spectrometer.
9. Use of an oligomer array according to claim 1 for the hybridization of DNA
fragments after prior amplification.
10. The use according to claim 9, further characterized in that the DNA is treated with a bisulfite solution (or hydrogen sulfite solution, disulfite solution) prior to the amplification.
11. The use of an oligomer array according to claim 1 for the detection of cytosine methylations in genomic DNA.
CA2390312A 1999-11-25 2000-11-24 Oligomer array with pna and/or dna oligomers on a surface Expired - Fee Related CA2390312C (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
DE19957827A DE19957827C2 (en) 1999-11-25 1999-11-25 Use of an oligomer array with PNA and / or DNA oligomers on a surface
DE19957827.3 1999-11-25
PCT/DE2000/004301 WO2001038565A2 (en) 1999-11-25 2000-11-24 Oligomer array with pna and/or dna oligomers on a surface

Publications (2)

Publication Number Publication Date
CA2390312A1 true CA2390312A1 (en) 2001-05-31
CA2390312C CA2390312C (en) 2011-05-31

Family

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Family Applications (1)

Application Number Title Priority Date Filing Date
CA2390312A Expired - Fee Related CA2390312C (en) 1999-11-25 2000-11-24 Oligomer array with pna and/or dna oligomers on a surface

Country Status (16)

Country Link
US (1) US6936419B1 (en)
EP (2) EP1232287B1 (en)
JP (2) JP2003514570A (en)
CN (1) CN1413263B (en)
AT (1) ATE362548T1 (en)
AU (1) AU784238B2 (en)
CA (1) CA2390312C (en)
DE (2) DE19957827C2 (en)
DK (1) DK1232287T3 (en)
ES (1) ES2287049T3 (en)
IL (1) IL149801A0 (en)
IS (1) IS2445B (en)
MX (1) MXPA02005221A (en)
NZ (1) NZ518548A (en)
PT (1) PT1232287E (en)
WO (1) WO2001038565A2 (en)

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Publication number Publication date
WO2001038565A3 (en) 2001-11-15
CN1413263B (en) 2012-07-04
AU2827001A (en) 2001-06-04
IL149801A0 (en) 2002-11-10
DE19957827A1 (en) 2001-06-21
ES2287049T3 (en) 2007-12-16
IS2445B (en) 2008-11-15
EP1816216A2 (en) 2007-08-08
ATE362548T1 (en) 2007-06-15
PT1232287E (en) 2007-08-21
DK1232287T3 (en) 2007-09-24
EP1232287B1 (en) 2007-05-16
NZ518548A (en) 2004-12-24
WO2001038565A2 (en) 2001-05-31
DE50014333D1 (en) 2007-06-28
JP2003514570A (en) 2003-04-22
EP1232287A2 (en) 2002-08-21
DE19957827C2 (en) 2003-06-12
IS6364A (en) 2002-04-26
AU784238B2 (en) 2006-02-23
EP1816216A3 (en) 2009-06-03
CN1413263A (en) 2003-04-23
JP2007175051A (en) 2007-07-12
CA2390312C (en) 2011-05-31
US6936419B1 (en) 2005-08-30
MXPA02005221A (en) 2004-08-23

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