DK3066219T3 - Fremgangsmåder til påvisning af oligonukleotider - Google Patents
Fremgangsmåder til påvisning af oligonukleotider Download PDFInfo
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- DK3066219T3 DK3066219T3 DK14860026.5T DK14860026T DK3066219T3 DK 3066219 T3 DK3066219 T3 DK 3066219T3 DK 14860026 T DK14860026 T DK 14860026T DK 3066219 T3 DK3066219 T3 DK 3066219T3
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- certain embodiments
- oligonucleotide
- modified
- sugar
- nucleosides
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- 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
- C12Q1/6834—Enzymatic or biochemical coupling of nucleic acids to a solid phase
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- 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
- C12Q1/6834—Enzymatic or biochemical coupling of nucleic acids to a solid phase
- C12Q1/6837—Enzymatic or biochemical coupling of nucleic acids to a solid phase using probe arrays or probe chips
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- 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
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- 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
- C12Q1/6825—Nucleic acid detection involving sensors
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Zoology (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Analytical Chemistry (AREA)
- Molecular Biology (AREA)
- Microbiology (AREA)
- Immunology (AREA)
- Biotechnology (AREA)
- Biochemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Physics & Mathematics (AREA)
- Biophysics (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Claims (17)
1. Fremgangsmåde til påvisning eller kvantificering af et måloligonukleotid i en legemsvæske eller -ekstrakt hvor måloligonukleotidet er 14 til 40 nukleosider i længde og omfatter mindst ét modificeret nukleosid omfattende en modificeret sukkergruppe der giver øget bindingsaffinitet til en målnukleinsyre, omfattende: at danne en testprøve ved at bringe legemsvæsken eller -ekstrakt i kontakt med en indfangningsprobe, hvor: indfangningsproben er komplementær med en første del af måloligonukleotidet; og indfangningsproben omfatter en bindingsgruppe, hvor bindingsgruppen er kovalent bundet til indfangningsproben; testprøven bringes i kontakt med en fast bærer, hvor den faste bærer omfatter en bindingspartner af bindingsgruppen af indfangningsproben; testprøven bringes i kontakt med en påvisningsprobe, hvor: påvisningsproben er komplementær med en anden del af måloligonukleotidet, hvor den første del og den anden del af måloligonukleotidet ikke overlapper; og påvisningsproben omfatter en elektrochemiluminescerende gruppe, hvor den elektrochemiluminescerende gruppe er kovalent bundet til påvisningsproben; vaskning af testprøven for at fjerne ubundet probe; detektere tilstedeværelsen eller mængde af den elektrochemiluminescerende gruppe i testprøven; og derved identificere eller kvantificere måloligonukleotidet i legemsvæsken eller -ekstrakt.
2. Fremgangsmåden ifølge krav 1, hvor det mindst ene modificerede nukleosid omfattende en modificeret sukkergruppe der giver øget bindingsaffinitet til en målnukleinsyre omfatter en 2'-O-methoxyethylmodifikation.
3. Fremgangsmåden ifølge krav 1 eller 2, hvor det mindst ene modificerede nukleosid omfattende en modificeret sukkergruppe der giver øget bindingsaffinitet til en målnukleinsyre omfatter et bicyklisk nukleosid.
4. Fremgangsmåden ifølge et hvilket som helst af kravene 1-3, hvor indfangningsproben omfatter mindst én sukkermodifikation.
5. Fremgangsmåden ifølge et hvilket som helst af kravene 1-4, hvor påvisningsproben omfatter mindst én sukkermodifikation.
6. Fremgangsmåden ifølge et hvilket som helst af kravene 1-5, hvor indfangningsproben omfatter mindst én 2'-O-methoxyethyl sukkermodifikation.
7. Fremgangsmåden ifølge et hvilket som helst af kravene 1-6, hvor indfangningsproben omfatter mindst én cEt-sukkermodifikation.
8. Fremgangsmåden ifølge et hvilket som helst af kravene 1-7, hvor indfangningsproben omfatter mindst én 2'-F-sukkermodifikation.
9. Fremgangsmåden ifølge et hvilket som helst af kravene 1-8, hvor påvisningsproben omfatter mindst én 2'-O-methoxyethyl-sukkermodifikation.
10. Fremgangsmåden ifølge et hvilket som helst af kravene 1-9, hvor påvisningsproben omfatter mindst én cEt-sukkermodifikation.
11. Fremgangsmåden ifølge et hvilket som helst af kravene 1-10, hvor påvisningsproben omfatter mindst én 2'-F sukkermodifikation.
12. Fremgangsmåden ifølge et hvilket som helst af kravene 1-11, hvor legemsvæsken er cerebrospinalvæske.
13. Fremgangsmåden ifølge et hvilket som helst af kravene 1-12, hvor den elektrochemiluminescerende gruppe er tris(2,2-bipyridin) Ruthenium (II) tag.
14. Fremgangsmåden ifølge et hvilket som helst af kravene 1-13, hvor fremgangsmåden har en sensitivitet på mindre end 1 ng/ml af måloligonukleotidet.
15. Fremgangsmåden ifølge et hvilket som helst af kravene 1-14, yderligere omfattende at bringe testprøven i kontakt med en protease, eventuelt hvor proteasen er Proteinase K.
16. Fremgangsmåden ifølge et hvilket som helst af kravene 1-15, hvor indfangnings- og påvisningsproberne hver er 7-10 nukleotider i længde.
17. Fremgangsmåden ifølge et hvilket som helst af kravene 1-16, hvor måloligonukleotidet er 18-40, 20-40, 10-30, 14-30, 18-30, 20-30, 10-22, 14-22, 18-22 eller 20-22 nukleosider i længde.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201361902112P | 2013-11-08 | 2013-11-08 | |
PCT/US2014/064874 WO2015070173A1 (en) | 2013-11-08 | 2014-11-10 | Compounds and methods for detecting oligonucleotides |
Publications (1)
Publication Number | Publication Date |
---|---|
DK3066219T3 true DK3066219T3 (da) | 2019-03-11 |
Family
ID=53042205
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DK14860026.5T DK3066219T3 (da) | 2013-11-08 | 2014-11-10 | Fremgangsmåder til påvisning af oligonukleotider |
Country Status (4)
Country | Link |
---|---|
US (1) | US10752940B2 (da) |
EP (1) | EP3066219B1 (da) |
DK (1) | DK3066219T3 (da) |
WO (1) | WO2015070173A1 (da) |
Families Citing this family (8)
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CA3011894A1 (en) | 2016-01-31 | 2017-08-03 | University Of Massachusetts | Branched oligonucleotides |
WO2018031933A2 (en) | 2016-08-12 | 2018-02-15 | University Of Massachusetts | Conjugated oligonucleotides |
EP4035659A1 (en) | 2016-11-29 | 2022-08-03 | PureTech LYT, Inc. | Exosomes for delivery of therapeutic agents |
SG11202101288TA (en) | 2018-08-10 | 2021-03-30 | Univ Massachusetts | Modified oligonucleotides targeting snps |
WO2021087164A1 (en) * | 2019-10-30 | 2021-05-06 | Shire Human Genetic Therapies, Inc. | Methods for detecting oligonucleotides |
WO2021146548A1 (en) * | 2020-01-17 | 2021-07-22 | Anastasia Khvorova | Universal dynamic pharmacokinetic-modifying anchors |
WO2022271786A1 (en) | 2021-06-23 | 2022-12-29 | University Of Massachusetts | Optimized anti-flt1 oligonucleotide compounds for treatment of preeclampsia and other angiogenic disorders |
WO2023129884A1 (en) * | 2021-12-30 | 2023-07-06 | Meso Scale Technologies, Llc. | Methods for electrochemiluminescence detection |
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2014
- 2014-11-10 US US15/034,508 patent/US10752940B2/en active Active
- 2014-11-10 EP EP14860026.5A patent/EP3066219B1/en active Active
- 2014-11-10 WO PCT/US2014/064874 patent/WO2015070173A1/en active Application Filing
- 2014-11-10 DK DK14860026.5T patent/DK3066219T3/da active
Also Published As
Publication number | Publication date |
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EP3066219A4 (en) | 2017-06-14 |
WO2015070173A1 (en) | 2015-05-14 |
US20160281148A1 (en) | 2016-09-29 |
EP3066219B1 (en) | 2018-12-26 |
US10752940B2 (en) | 2020-08-25 |
EP3066219A1 (en) | 2016-09-14 |
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