SG10201909816PA - Methods of polynucleotide preparation using multivalent cation salt compositions - Google Patents

Methods of polynucleotide preparation using multivalent cation salt compositions

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Publication number
SG10201909816PA
SG10201909816PA SG10201909816PA SG10201909816PA SG 10201909816P A SG10201909816P A SG 10201909816PA SG 10201909816P A SG10201909816P A SG 10201909816PA SG 10201909816P A SG10201909816P A SG 10201909816PA
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SG
Singapore
Prior art keywords
polynucleotide
salt
multivalent cation
methods
preparation
Prior art date
Application number
Inventor
Premchandran Ramiya
Original Assignee
Geron Corp
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Publication date
Application filed by Geron Corp filed Critical Geron Corp
Publication of SG10201909816PA publication Critical patent/SG10201909816PA/en

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    • CCHEMISTRY; METALLURGY
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    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N15/00Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09Recombinant DNA-technology
    • C12N15/10Processes for the isolation, preparation or purification of DNA or RNA
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
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    • C12N15/00Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09Recombinant DNA-technology
    • C12N15/11DNA or RNA fragments; Modified forms thereof; Non-coding nucleic acids having a biological activity
    • C12N15/113Non-coding nucleic acids modulating the expression of genes, e.g. antisense oligonucleotides; Antisense DNA or RNA; Triplex- forming oligonucleotides; Catalytic nucleic acids, e.g. ribozymes; Nucleic acids used in co-suppression or gene silencing
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
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    • C12N15/00Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09Recombinant DNA-technology
    • C12N15/10Processes for the isolation, preparation or purification of DNA or RNA
    • C12N15/1003Extracting or separating nucleic acids from biological samples, e.g. pure separation or isolation methods; Conditions, buffers or apparatuses therefor
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N15/00Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09Recombinant DNA-technology
    • C12N15/10Processes for the isolation, preparation or purification of DNA or RNA
    • C12N15/1003Extracting or separating nucleic acids from biological samples, e.g. pure separation or isolation methods; Conditions, buffers or apparatuses therefor
    • C12N15/1006Extracting or separating nucleic acids from biological samples, e.g. pure separation or isolation methods; Conditions, buffers or apparatuses therefor by means of a solid support carrier, e.g. particles, polymers
    • C12N15/101Extracting or separating nucleic acids from biological samples, e.g. pure separation or isolation methods; Conditions, buffers or apparatuses therefor by means of a solid support carrier, e.g. particles, polymers by chromatography, e.g. electrophoresis, ion-exchange, reverse phase
    • CCHEMISTRY; METALLURGY
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    • C12N15/00Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09Recombinant DNA-technology
    • C12N15/11DNA or RNA fragments; Modified forms thereof; Non-coding nucleic acids having a biological activity
    • C12N15/113Non-coding nucleic acids modulating the expression of genes, e.g. antisense oligonucleotides; Antisense DNA or RNA; Triplex- forming oligonucleotides; Catalytic nucleic acids, e.g. ribozymes; Nucleic acids used in co-suppression or gene silencing
    • C12N15/1137Non-coding nucleic acids modulating the expression of genes, e.g. antisense oligonucleotides; Antisense DNA or RNA; Triplex- forming oligonucleotides; Catalytic nucleic acids, e.g. ribozymes; Nucleic acids used in co-suppression or gene silencing against enzymes
    • CCHEMISTRY; METALLURGY
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    • C12PFERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P19/00Preparation of compounds containing saccharide radicals
    • C12P19/26Preparation of nitrogen-containing carbohydrates
    • C12P19/28N-glycosides
    • C12P19/30Nucleotides
    • C12P19/34Polynucleotides, e.g. nucleic acids, oligoribonucleotides
    • 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
    • C12Q1/6806Preparing nucleic acids for analysis, e.g. for polymerase chain reaction [PCR] assay
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
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    • C12N2310/00Structure or type of the nucleic acid
    • C12N2310/10Type of nucleic acid
    • C12N2310/11Antisense
    • C12N2310/113Antisense targeting other non-coding nucleic acids, e.g. antagomirs
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
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    • C12N2310/00Structure or type of the nucleic acid
    • C12N2310/30Chemical structure
    • C12N2310/31Chemical structure of the backbone
    • C12N2310/314Phosphoramidates
    • C12N2310/3145Phosphoramidates with the nitrogen in 3' or 5'-position
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
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    • C12N2310/00Structure or type of the nucleic acid
    • C12N2310/30Chemical structure
    • C12N2310/35Nature of the modification
    • C12N2310/351Conjugate
    • C12N2310/3515Lipophilic moiety, e.g. cholesterol
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12YENZYMES
    • C12Y207/00Transferases transferring phosphorus-containing groups (2.7)
    • C12Y207/07Nucleotidyltransferases (2.7.7)
    • C12Y207/07049RNA-directed DNA polymerase (2.7.7.49), i.e. telomerase or reverse-transcriptase

Abstract

METHODS OF POLYNUCLEOTIDE PREPARATION USING MULTIVALENT CATION SALT COMPOSITIONS Aspects of the disclosure include methods for the preparation of a polynucleotide. In some embodiments, the method includes contacting a first polynucleotide composition including: a polynucleotide having a sequence of 7 or more nucleoside subunits and at least two of the nucleoside subunits are joined by a N3′→P5′ thiophosphoramidate inter-subunit linkage; and non-target synthetic products and reagents; with a multivalent cation salt to precipitate a polynucleotide salt including at least one multivalent cation counterion; and separating the polynucleotide salt from the contacted first polynucleotide composition to produce a second polynucleotide composition including the polynucleotide salt. In certain embodiments, the method further includes contacting the polynucleotide salt with a reverse phase chromatography support; and eluting from the chromatography support a third polynucleotide composition including the polynucleotide. Also provided are compositions including a salt of the polynucleotide including at least one multivalent cation counterion. FIG. 2
SG10201909816P 2015-04-23 2016-04-21 Methods of polynucleotide preparation using multivalent cation salt compositions SG10201909816PA (en)

Applications Claiming Priority (1)

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US201562151891P 2015-04-23 2015-04-23

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EP (1) EP3286203B1 (en)
JP (3) JP2018513127A (en)
KR (1) KR102401252B1 (en)
CN (2) CN107429247B (en)
AU (2) AU2016250576C1 (en)
BR (1) BR112017019627B1 (en)
CA (1) CA2978191C (en)
CL (1) CL2017002314A1 (en)
CO (1) CO2017009217A2 (en)
CY (1) CY1123197T1 (en)
DK (1) DK3286203T3 (en)
EA (1) EA035885B1 (en)
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HK (1) HK1251234A1 (en)
HR (1) HRP20201218T1 (en)
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PE (2) PE20221275A1 (en)
PH (1) PH12017501927A1 (en)
PT (1) PT3286203T (en)
RS (1) RS60645B1 (en)
SA (1) SA517390103B1 (en)
SG (2) SG10201909816PA (en)
SI (1) SI3286203T1 (en)
TN (1) TN2017000411A1 (en)
TW (1) TWI736532B (en)
UA (1) UA124521C2 (en)
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ZA (1) ZA201706041B (en)

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EP3668977A4 (en) * 2017-08-18 2021-04-21 Modernatx, Inc. Analytical hplc methods
CN111542606A (en) * 2017-09-22 2020-08-14 科罗拉多州立大学董事会法人团体 Thiomorpholino oligonucleotides for treating muscular dystrophy
JP2021507695A (en) * 2017-12-18 2021-02-25 ヴェンタナ メディカル システムズ, インク. Peptide nucleic acid conjugate

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BR112017019627B1 (en) 2022-11-29
MD3286203T2 (en) 2020-08-31
US10745687B2 (en) 2020-08-18
AU2016250576C1 (en) 2021-05-06
BR112017019627A2 (en) 2018-05-15
CN107429247A (en) 2017-12-01
US20200339975A1 (en) 2020-10-29
KR20170138399A (en) 2017-12-15
ZA201706041B (en) 2020-11-25
HUE051148T2 (en) 2021-03-01
EA035885B1 (en) 2020-08-27
HRP20201218T1 (en) 2020-12-11
RS60645B1 (en) 2020-09-30
AU2021202803A1 (en) 2021-06-03
MY187804A (en) 2021-10-26
JP2021152079A (en) 2021-09-30
CN107429247B (en) 2021-08-13
CO2017009217A2 (en) 2018-02-20
LT3286203T (en) 2020-07-27
PE20171785A1 (en) 2017-12-27
AU2016250576B2 (en) 2021-02-04
TWI736532B (en) 2021-08-21
CL2017002314A1 (en) 2018-05-04
SG11201707893RA (en) 2017-11-29
AU2016250576A1 (en) 2017-09-21
US20160312227A1 (en) 2016-10-27
US11441144B2 (en) 2022-09-13
IL254222A0 (en) 2017-10-31
CY1123197T1 (en) 2021-10-29
TW201706284A (en) 2017-02-16
NZ735042A (en) 2021-11-26
PH12017501927A1 (en) 2018-03-05
EP3286203A1 (en) 2018-02-28
EA201791753A1 (en) 2018-04-30
UA124521C2 (en) 2021-10-05
TN2017000411A1 (en) 2019-01-16
EP3286203B1 (en) 2020-05-06
CA2978191C (en) 2022-10-04
ES2798270T3 (en) 2020-12-10
MA42569B1 (en) 2020-08-31
ME03811B (en) 2021-04-20
MX2017011642A (en) 2017-11-02
JP2022168017A (en) 2022-11-04
HK1251234A1 (en) 2019-01-25
KR102401252B1 (en) 2022-05-24
DK3286203T3 (en) 2020-06-02
PE20221275A1 (en) 2022-09-01
SI3286203T1 (en) 2020-10-30
CN113564168A (en) 2021-10-29
SA517390103B1 (en) 2021-07-14
PT3286203T (en) 2020-07-08
WO2016172346A1 (en) 2016-10-27
MA42157A (en) 2018-02-28
JP2018513127A (en) 2018-05-24
CA2978191A1 (en) 2016-10-27

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