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ES2684587T3 - Producción de bibliotecas químicas codificadas - Google Patents

Producción de bibliotecas químicas codificadas Download PDF

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Publication number
ES2684587T3
ES2684587T3 ES14824390T ES14824390T ES2684587T3 ES 2684587 T3 ES2684587 T3 ES 2684587T3 ES 14824390 T ES14824390 T ES 14824390T ES 14824390 T ES14824390 T ES 14824390T ES 2684587 T3 ES2684587 T3 ES 2684587T3
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ES
Spain
Prior art keywords
nucleic acid
strands
coupled
strand
chemical
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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.)
Active
Application number
ES14824390T
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English (en)
Inventor
Willy DECURTINS
Raphael FRANZINI
Dario Neri
Jörg Scheuermann
Moreno WICHERT
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Philochem AG
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Philochem AG
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First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=50071234&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=ES2684587(T3) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Philochem AG filed Critical Philochem AG
Application granted granted Critical
Publication of ES2684587T3 publication Critical patent/ES2684587T3/es
Active legal-status Critical Current
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Classifications

    • 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
    • C12N15/1034Isolating an individual clone by screening libraries
    • C12N15/1068Template (nucleic acid) mediated chemical library synthesis, e.g. chemical and enzymatical DNA-templated organic molecule synthesis, libraries prepared by non ribosomal polypeptide synthesis [NRPS], DNA/RNA-polymerase mediated polypeptide synthesis
    • CCHEMISTRY; METALLURGY
    • C40COMBINATORIAL TECHNOLOGY
    • C40BCOMBINATORIAL CHEMISTRY; LIBRARIES, e.g. CHEMICAL LIBRARIES
    • C40B20/00Methods specially adapted for identifying library members
    • C40B20/06Methods specially adapted for identifying library members using iterative deconvolution techniques
    • CCHEMISTRY; METALLURGY
    • C40COMBINATORIAL TECHNOLOGY
    • C40BCOMBINATORIAL CHEMISTRY; LIBRARIES, e.g. CHEMICAL LIBRARIES
    • C40B40/00Libraries per se, e.g. arrays, mixtures
    • C40B40/04Libraries containing only organic compounds
    • C40B40/06Libraries containing nucleotides or polynucleotides, or derivatives thereof
    • CCHEMISTRY; METALLURGY
    • C40COMBINATORIAL TECHNOLOGY
    • C40BCOMBINATORIAL CHEMISTRY; LIBRARIES, e.g. CHEMICAL LIBRARIES
    • C40B50/00Methods of creating libraries, e.g. combinatorial synthesis
    • C40B50/08Liquid phase synthesis, i.e. wherein all library building blocks are in liquid phase or in solution during library creation; Particular methods of cleavage from the liquid support
    • C40B50/10Liquid phase synthesis, i.e. wherein all library building blocks are in liquid phase or in solution during library creation; Particular methods of cleavage from the liquid support involving encoding steps
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/58Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving labelled substances
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07HSUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H21/00Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids
    • C07H21/02Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids with ribosyl as saccharide radical
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07HSUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H21/00Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids
    • C07H21/04Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids with deoxyribosyl as saccharide radical
    • 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
    • C12Q1/6869Methods for sequencing
    • C12Q1/6874Methods for sequencing involving nucleic acid arrays, e.g. sequencing by hybridisation

Landscapes

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

Abstract

Método de producción de una biblioteca química codificada por ácido nucleico que comprende; (i) producir una sub-biblioteca según un método que comprende; (a) proporcionar una población de primeras hebras de ácido nucleico, estando acoplada o pudiendo acoplarse cada hebra de ácido nucleico a un miembro de una primera población diversa de restos químicos y que comprende un espaciador no hibridable, (b) poner en contacto las primeras hebras de ácido nucleico con oligonucleótidos identificadores que comprenden una primera secuencia codificante y uno o más oligonucleótidos adaptadores, de manera que el uno o más oligonucleótidos adaptadores se hibridan con las hebras de ácido nucleico y los oligonucleótidos identificadores para formar un complejo parcialmente bicatenario, en el que cada primera hebra de ácido nucleico se pone en contacto con un oligonucleótido identificador que comprende una primera secuencia codificante que codifica para un resto químico que está acoplado o puede acoplarse a la primera hebra de ácido nucleico, y; en el que cada uno de dicho uno o más oligonucleótidos adaptadores se hibrida con más de una primera hebra de ácido nucleico en la población y más de un oligonucleótido identificador diferente, (c) ligar las primeras hebras de ácido nucleico con los oligonucleótidos identificadores en los complejos parcialmente bicatenarios, de manera que los oligonucleótidos identificadores se incorporan en las primeras hebras de ácido nucleico, produciendo de ese modo una sub-biblioteca que comprende primeras hebras de ácido nucleico acopladas o que pueden acoplarse a un miembro de una población diversa de restos químicos, en el que cada primera hebra de ácido nucleico comprende una primera secuencia codificante que codifica para el resto químico que está acoplado a la primera hebra de ácido nucleico y el espaciador no hibridable; (ii) hibridar las primeras hebras de ácido nucleico con segundas hebras de ácido nucleico para formar complejos bicatenarios, en el que las segundas hebras de ácido nucleico se acoplan con una segunda población diversa de restos químicos, comprendiendo cada segunda hebra de ácido nucleico una segunda secuencia codificante que codifica para el resto químico que está acoplado a la misma, correspondiendo la posición de la segunda secuencia codificante en las segundas hebras de ácido nucleico en el complejo bicatenario a la posición del espaciador en las primeras hebras de ácido nucleico en los complejos bicatenarios, de manera que las segundas secuencias codificantes no se hibridan preferentemente con las primeras hebras de ácido nucleico, y (iii) extender las segundas hebras de ácido nucleico a lo largo de las hebras de ácido nucleico para producir una biblioteca que comprende miembros que tienen una molécula de ácido nucleico bicatenario que comprende las hebras de ácido nucleico primera y segunda; estando acoplada la primera población diversa de restos químicos a las primeras hebras de ácido nucleico y estando acoplada la segunda población diversa de restos químicos a las segundas hebras de ácido nucleico, dichos restos químicos forman farmacóforos en los miembros de la biblioteca, en el que cada segunda hebra de ácido nucleico comprende secuencias codificantes primera y segunda que codifican para los restos químicos de las poblaciones diversas primera y segunda.
ES14824390T 2013-12-20 2014-12-11 Producción de bibliotecas químicas codificadas Active ES2684587T3 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GBGB1322692.3A GB201322692D0 (en) 2013-12-20 2013-12-20 Production of encoded chemical libraries
PCT/EP2014/077403 WO2015091207A1 (en) 2013-12-20 2014-12-11 Production of encoded chemical libraries

Publications (1)

Publication Number Publication Date
ES2684587T3 true ES2684587T3 (es) 2018-10-03

Family

ID=50071234

Family Applications (1)

Application Number Title Priority Date Filing Date
ES14824390T Active ES2684587T3 (es) 2013-12-20 2014-12-11 Producción de bibliotecas químicas codificadas

Country Status (7)

Country Link
US (2) US10240147B2 (es)
EP (1) EP3083957B1 (es)
AU (1) AU2014365162B2 (es)
CA (1) CA2934126C (es)
ES (1) ES2684587T3 (es)
GB (1) GB201322692D0 (es)
WO (1) WO2015091207A1 (es)

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2010094036A1 (en) 2009-02-13 2010-08-19 X-Chem, Inc. Methods of creating and screening dna-encoded libraries
SG10201605812YA (en) 2011-09-07 2016-09-29 Chem Inc X Methods for tagging dna-encoded libraries
KR102146721B1 (ko) * 2012-07-13 2020-08-21 엑스-켐, 인크. 폴리머라제에 의해 판독가능하지 않은 코딩 올리고뉴클레오티드 연결을 갖는 dna-코딩된 라이브러리
GB201322692D0 (en) 2013-12-20 2014-02-05 Philochem Ag Production of encoded chemical libraries
GB201603789D0 (en) 2016-03-04 2016-04-20 Apta Biosciences Ltd Oligonucleotides and methods for preparing
WO2017214067A1 (en) * 2016-06-05 2017-12-14 Dice Molecules Sv, Llc Methods of routing, compositions and uses thereof
WO2017218293A1 (en) 2016-06-16 2017-12-21 Richard Edward Watts Oligonucleotide directed and recorded combinatorial synthesis of encoded probe molecules
US20200190507A1 (en) * 2016-11-10 2020-06-18 The Scripps Research Institute Encoded Solid Phase Compound Library with Polynucleotide Based Barcoding
GB201622222D0 (en) 2016-12-23 2017-02-08 Cs Genetics Ltd Reagents and methods for molecular barcoding of nucleic acids of single cells
CN110325491B (zh) * 2017-03-17 2022-04-19 成都先导药物开发股份有限公司 编码库的合成方法及组合物
WO2018204420A1 (en) 2017-05-02 2018-11-08 Haystack Sciences Corporation Molecules for verifying oligonucleotide directed combinatorial synthesis and methods of making and using the same
WO2020092614A1 (en) * 2018-10-31 2020-05-07 Rutgers, The State University Of New Jersey Gramc: genome-scale reporter assay method for cis-regulatory modules
GB201821109D0 (en) 2018-12-21 2019-02-06 Philochem Ag Nucleic acid encoded chemical libraries
CN110346493B (zh) * 2019-05-23 2021-01-05 中国人民解放军军事科学院军事医学研究院 检测猕猴血浆中中期因子反义寡核苷酸含量的方法
CN112575389B (zh) * 2019-09-30 2023-09-19 成都先导药物开发股份有限公司 一种dna编码化合物库的液相色谱纯化方法
CN114790578A (zh) * 2021-01-26 2022-07-26 成都先导药物开发股份有限公司 一种dna编码化合物库的rna靶标筛选方法
WO2024069235A2 (en) 2022-09-30 2024-04-04 Sixfold Bioscience Ltd. Compositions containing oligonucleotides with theranostic applications

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GB201322692D0 (en) 2013-12-20 2014-02-05 Philochem Ag Production of encoded chemical libraries

Also Published As

Publication number Publication date
CA2934126A1 (en) 2015-06-25
EP3083957B1 (en) 2018-05-23
US20170009226A1 (en) 2017-01-12
AU2014365162A1 (en) 2016-07-21
WO2015091207A1 (en) 2015-06-25
AU2014365162B2 (en) 2018-03-08
CA2934126C (en) 2019-04-23
GB201322692D0 (en) 2014-02-05
US10240147B2 (en) 2019-03-26
US20200123534A1 (en) 2020-04-23
EP3083957A1 (en) 2016-10-26

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