MA42157A - Procédés de préparation de polynucléotides à l'aide de compositions de sel cationique multivalent - Google Patents

Procédés de préparation de polynucléotides à l'aide de compositions de sel cationique multivalent

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Publication number
MA42157A
MA42157A MA042157A MA42157A MA42157A MA 42157 A MA42157 A MA 42157A MA 042157 A MA042157 A MA 042157A MA 42157 A MA42157 A MA 42157A MA 42157 A MA42157 A MA 42157A
Authority
MA
Morocco
Prior art keywords
polynucleotide
salt
preparation
composition
polynucleotides
Prior art date
Application number
MA042157A
Other languages
English (en)
Inventor
Premchandran H Ramiya
Original Assignee
Geron Corp
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 Geron Corp filed Critical Geron Corp
Publication of MA42157A publication Critical patent/MA42157A/fr

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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
    • 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
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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
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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
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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
    • 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
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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
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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
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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
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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
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    • 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

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  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Biomedical Technology (AREA)
  • Organic Chemistry (AREA)
  • Zoology (AREA)
  • Wood Science & Technology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Engineering & Computer Science (AREA)
  • Biotechnology (AREA)
  • Molecular Biology (AREA)
  • Biochemistry (AREA)
  • Microbiology (AREA)
  • General Health & Medical Sciences (AREA)
  • Physics & Mathematics (AREA)
  • Biophysics (AREA)
  • Plant Pathology (AREA)
  • Analytical Chemistry (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Virology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Immunology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Saccharide Compounds (AREA)
  • Treatment Of Liquids With Adsorbents In General (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)

Abstract

Des aspects de la description comprennent des procédés pour la préparation d'un polynucléotide. Dans certains modes de réalisation, le procédé comprend la mise en contact d'une première composition polynucléotidique comprenant: un polynucléotide ayant une séquence de 7 sous-unités nucléosidiques ou plus et au moins deux des sous-unités nucléosidiques sont jointes par une liaison inter-sous-unité thiophosphoramidate n3 '→ p5'; et des produits synthétiques non ciblés et des réactifs; avec un sel de cation multivalent pour précipiter un sel de polynucléotide comprenant au moins un contre-ion de cation multivalent; et séparer le sel polynucléotidique de la première composition polynucléotidique mise en contact pour produire une seconde composition polynucléotidique comprenant le sel polynucléotidique. Dans certains modes de réalisation, le procédé comprend en outre la mise en contact du sel de polynucléotide avec un support de chromatographie en phase inverse; et en éluant à partir du support de chromatographie une troisième composition polynucléotidique comprenant le polynucléotide. L'invention concerne également des compositions comprenant un sel du polynucléotide comprenant au moins un contre-ion de cation multivalent.
MA042157A 2015-04-23 2016-04-21 Procédés de préparation de polynucléotides à l'aide de compositions de sel cationique multivalent MA42157A (fr)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US201562151891P 2015-04-23 2015-04-23

Publications (1)

Publication Number Publication Date
MA42157A true MA42157A (fr) 2018-02-28

Family

ID=55911083

Family Applications (2)

Application Number Title Priority Date Filing Date
MA042157A MA42157A (fr) 2015-04-23 2016-04-21 Procédés de préparation de polynucléotides à l'aide de compositions de sel cationique multivalent
MA42569A MA42569B1 (fr) 2015-04-23 2016-04-21 Procédés de préparation de polynucléotides à l'aide de compositions de sel cationique multivalent

Family Applications After (1)

Application Number Title Priority Date Filing Date
MA42569A MA42569B1 (fr) 2015-04-23 2016-04-21 Procédés de préparation de polynucléotides à l'aide de compositions de sel cationique multivalent

Country Status (36)

Country Link
US (2) US10745687B2 (fr)
EP (1) EP3286203B1 (fr)
JP (3) JP2018513127A (fr)
KR (1) KR102401252B1 (fr)
CN (2) CN113564168A (fr)
AU (2) AU2016250576C1 (fr)
BR (1) BR112017019627B1 (fr)
CA (1) CA2978191C (fr)
CL (1) CL2017002314A1 (fr)
CO (1) CO2017009217A2 (fr)
CY (1) CY1123197T1 (fr)
DK (1) DK3286203T3 (fr)
EA (1) EA035885B1 (fr)
ES (1) ES2798270T3 (fr)
HK (1) HK1251234A1 (fr)
HR (1) HRP20201218T1 (fr)
HU (1) HUE051148T2 (fr)
IL (1) IL254222A0 (fr)
LT (1) LT3286203T (fr)
MA (2) MA42157A (fr)
MD (1) MD3286203T2 (fr)
ME (1) ME03811B (fr)
MX (1) MX2017011642A (fr)
MY (1) MY187804A (fr)
PE (2) PE20221275A1 (fr)
PH (1) PH12017501927A1 (fr)
PT (1) PT3286203T (fr)
RS (1) RS60645B1 (fr)
SA (1) SA517390103B1 (fr)
SG (2) SG11201707893RA (fr)
SI (1) SI3286203T1 (fr)
TN (1) TN2017000411A1 (fr)
TW (1) TWI736532B (fr)
UA (1) UA124521C2 (fr)
WO (1) WO2016172346A1 (fr)
ZA (1) ZA201706041B (fr)

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SI3286203T1 (sl) 2015-04-23 2020-10-30 Geron Corporation Metode priprave polinukleotida, z uporabo sestavkov multivalentne kationske soli
WO2018111967A1 (fr) 2016-12-13 2018-06-21 Modernatx, Inc. Purification par affinité d'arn
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WO2019036683A1 (fr) * 2017-08-18 2019-02-21 Modernatx, Inc. Procédés analytiques par hplc
EP3684933A4 (fr) * 2017-09-22 2021-06-23 The Regents of the University of Colorado, A Body Corporate Oligonucléotides thiomorpholino pour le traitement de la dystrophie musculaire
WO2019120635A1 (fr) * 2017-12-18 2019-06-27 Ventana Medical Systems, Inc. Conjugués à base d'acide nucléique peptidique

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CN107429247B (zh) 2021-08-13
PH12017501927A1 (en) 2018-03-05
RS60645B1 (sr) 2020-09-30
HUE051148T2 (hu) 2021-03-01
KR102401252B1 (ko) 2022-05-24
ZA201706041B (en) 2020-11-25
SI3286203T1 (sl) 2020-10-30
SG10201909816PA (en) 2019-11-28
IL254222A0 (en) 2017-10-31
PT3286203T (pt) 2020-07-08
PE20171785A1 (es) 2017-12-27
US20160312227A1 (en) 2016-10-27
CN113564168A (zh) 2021-10-29
EA201791753A1 (ru) 2018-04-30
WO2016172346A1 (fr) 2016-10-27
CA2978191C (fr) 2022-10-04
MD3286203T2 (ro) 2020-08-31
EA035885B1 (ru) 2020-08-27
BR112017019627A2 (pt) 2018-05-15
SA517390103B1 (ar) 2021-07-14
BR112017019627B1 (pt) 2022-11-29
TW201706284A (zh) 2017-02-16
AU2016250576B2 (en) 2021-02-04
CA2978191A1 (fr) 2016-10-27
TN2017000411A1 (en) 2019-01-16
NZ735042A (en) 2021-11-26
JP2021152079A (ja) 2021-09-30
SG11201707893RA (en) 2017-11-29
MX2017011642A (es) 2017-11-02
AU2016250576C1 (en) 2021-05-06
LT3286203T (lt) 2020-07-27
CN107429247A (zh) 2017-12-01
UA124521C2 (uk) 2021-10-05
ME03811B (fr) 2021-04-20
JP2018513127A (ja) 2018-05-24
CL2017002314A1 (es) 2018-05-04
MY187804A (en) 2021-10-26
JP2022168017A (ja) 2022-11-04
US10745687B2 (en) 2020-08-18
ES2798270T3 (es) 2020-12-10
KR20170138399A (ko) 2017-12-15
US20200339975A1 (en) 2020-10-29
CY1123197T1 (el) 2021-10-29
DK3286203T3 (da) 2020-06-02
AU2016250576A1 (en) 2017-09-21
TWI736532B (zh) 2021-08-21
HK1251234A1 (zh) 2019-01-25
CO2017009217A2 (es) 2018-02-20
US11441144B2 (en) 2022-09-13
AU2021202803A1 (en) 2021-06-03
MA42569B1 (fr) 2020-08-31
EP3286203A1 (fr) 2018-02-28
PE20221275A1 (es) 2022-09-01
HRP20201218T1 (hr) 2020-12-11
EP3286203B1 (fr) 2020-05-06

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