DK2593594T3 - Antistofbiblioteker - Google Patents

Antistofbiblioteker Download PDF

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Publication number
DK2593594T3
DK2593594T3 DK11807533.2T DK11807533T DK2593594T3 DK 2593594 T3 DK2593594 T3 DK 2593594T3 DK 11807533 T DK11807533 T DK 11807533T DK 2593594 T3 DK2593594 T3 DK 2593594T3
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sequences
library
segments
libraries
cdrh3
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DK11807533.2T
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Maximiliano Vasquez
Michael Feldhaus
Arvind Sivasubramanian
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Adimab Llc
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    • 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
    • C12N15/1089Design, preparation, screening or analysis of libraries using computer algorithms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K16/00Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • 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
    • G01N33/53Immunoassay; Biospecific binding assay; Materials therefor
    • G01N33/543Immunoassay; Biospecific binding assay; Materials therefor with an insoluble carrier for immobilising immunochemicals
    • GPHYSICS
    • G16INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
    • G16BBIOINFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR GENETIC OR PROTEIN-RELATED DATA PROCESSING IN COMPUTATIONAL MOLECULAR BIOLOGY
    • G16B35/00ICT specially adapted for in silico combinatorial libraries of nucleic acids, proteins or peptides
    • G16B35/20Screening of libraries
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K2317/00Immunoglobulins specific features
    • C07K2317/20Immunoglobulins specific features characterized by taxonomic origin
    • C07K2317/21Immunoglobulins specific features characterized by taxonomic origin from primates, e.g. man
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K2317/00Immunoglobulins specific features
    • C07K2317/50Immunoglobulins specific features characterized by immunoglobulin fragments
    • C07K2317/56Immunoglobulins specific features characterized by immunoglobulin fragments variable (Fv) region, i.e. VH and/or VL
    • C07K2317/565Complementarity determining region [CDR]
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K2317/00Immunoglobulins specific features
    • C07K2317/50Immunoglobulins specific features characterized by immunoglobulin fragments
    • C07K2317/56Immunoglobulins specific features characterized by immunoglobulin fragments variable (Fv) region, i.e. VH and/or VL
    • C07K2317/567Framework region [FR]
    • 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
    • C40B40/08Libraries containing RNA or DNA which encodes proteins, e.g. gene libraries
    • CCHEMISTRY; METALLURGY
    • C40COMBINATORIAL TECHNOLOGY
    • C40BCOMBINATORIAL CHEMISTRY; LIBRARIES, e.g. CHEMICAL LIBRARIES
    • C40B50/00Methods of creating libraries, e.g. combinatorial synthesis
    • C40B50/06Biochemical methods, e.g. using enzymes or whole viable microorganisms
    • GPHYSICS
    • G16INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
    • G16BBIOINFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR GENETIC OR PROTEIN-RELATED DATA PROCESSING IN COMPUTATIONAL MOLECULAR BIOLOGY
    • G16B35/00ICT specially adapted for in silico combinatorial libraries of nucleic acids, proteins or peptides
    • GPHYSICS
    • G16INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
    • G16CCOMPUTATIONAL CHEMISTRY; CHEMOINFORMATICS; COMPUTATIONAL MATERIALS SCIENCE
    • G16C20/00Chemoinformatics, i.e. ICT specially adapted for the handling of physicochemical or structural data of chemical particles, elements, compounds or mixtures
    • G16C20/60In silico combinatorial chemistry

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

Claims (16)

  1. ANTI STOFBIBLIOTEKER Patentkrav
    1. Fremgangsmåde til fremstilling af et bibliotek med syntetiske polynukleotider, som koder for polypeptider, der omfatter CDRH3-sekvenser, hvilken fremgangsmåde omfatter: (a) tilvejebringelse af en pulje af teoretiske segmenter, som indeholder TN1-, DH-, N2- og H3-JH-segmenter; (b) tilvejebringelse af et referencesæt af præimmune CDRH3-sekvenser med sekvensdiversiteter og længdediversiteter svarende til naturligt forekommende humane antistofsekvenser, før disse sekvenser har gennemgået negativ selektion og/eller hypermutation; (c) anvendelse af kombinationer af de TN1-, DH-, N2- og H3-JH-segmenter, som er indeholdt i puljen af teoretiske segmenter ifølge (a), til at identificere det eller de tætteste match med hver CDRFB-sekvens i referencesættet ifølge (b); (d) udvælgelse af segmenter fra det eller de i trin (c) identificerede tætteste match til inklusion i et syntetisk bibliotek; og fe) syntese af det syntetiske CDRFB-bibliotek.
  2. 2. Fremgangsmåde ifølge krav 1, hvor (a) de segmenter, der udvælges til inklusion i det syntetiske bibliotek, udvælges ud fra deres segmentanvendelsesvægt i referencesættet af CDRH3-sekvenser, (b) de segmenter, der udvælges til inklusion i det syntetiske bibliotek, udvælges ud fra en eller flere fysisk-kemiske egenskaber, (c) fremgangsmåden endvidere omfatter udvælgelse af yderligere TN1- og N2-segmenter, som forekommer i referencesættet, men ikke i puljen af teoretiske segmenter, (d) stopkodoner reduceres eller fjernes fra biblioteket, (e) de uparrede Cys-rester, N-bundne glycosyleringsmotiver og deamideringsmotiver reduceres eller fjernes fra bibliotekets translationsprodukter, (f) DH-segmenteme og H3-JH-segmenteme trunkeres gradvist inden matchning med CDRH3-sekvenserne i referencesættet, (g) fremgangsmåden endvidere omfatter indføring af et eller to degenererede kodoner i et segment udvalgt fra gruppen bestående af DH og N2 eller kombinationer deraf, eller (h) fremgangsmåden endvidere omfatter indføring af ét degenereret kodon i H3-JH-segmentet,
  3. 3. Bibliotek med syntetiske polynukleotider, som omfatter mindst ca, 104 polynukleotider, der koder for polypeptider, som omfatter forskellige CDRH3-sekvenser med strukturen: [TN 1 ] - [D H] - [N 2] ~ [H3 - JH], hvor: TN1 er et polypeptid, som omfatter et hvilket som helst af TNl-polypeptiderne fra tabellerne 10 og 18-26 eller et polypeptid, der er fremstillet ved translation af et hvilket som helst af TN 1 -polynukleotiderne fra tabellerne 25-26; DH er et polypeptid, som omfatter et hvilket som helst af DH-polypeptideme fra tabellerne 11, 17-25 og 28 eller et polypeptid, der er fremstillet ved translation af et hvilket som helst af de DH-kodende polynukleotider fra tabellerne 16, 25 og 27; N2 er et polypeptid, som omfatter et hvilket som helst af N2-polypeptideme fra tabellerne 12, 18-25 og 30 eller et polypeptid, der er fremstillet ved translation af et hvilket som helst af de N2-kodende polynukleotider fra tabellerne 25 og 29; og H3-JH er et polypeptid, som omfatter et hvilket som helst af H3-JH-polypeptiderne fra tabellerne 13, 15, 18-25 og 32 eller et polypeptid, der er fremstillet ved translation af et hvilket som helst af de H3-JH-kodende polynukleotider fra tabellerne 14, 25 og 31; hvor biblioteket er fremstillet ved fremgangsmåden ifølge krav 1.
  4. 4. Bibliotek ifølge krav 3, hvor polynukleotiderne koder for CDRH3- polypeptider, som er fremstillet ud fra TN1-, DH-, N2- og H3-JH-polypeptidsættene, der er anført i hvilke som helst af tabellerne 23-25.
  5. 5. Bibliotek ifølge krav 3, hvor polynukleotiderne koder for CDRH3- polypeptider, som er fremstillet ud fra TNl-polypeptidsættet, der er anført i tabel 26, DH-polypeptidsættet, der er anført i tabel 28, N2-polypeptidsættet, der er anført i tabel 30, og H3-JH-polypeptidsættet, der er anført i tabel 32.
  6. 6. Bibliotek ifølge krav 3, hvor antallet af N-bundne glycosyleringssteder, dearai deringsmotiver og/eller Cys-rester er reduceret eller fjernet i sammenligning med biblioteker, som er fremstillet ved amplifikation af et repertoire fra en biologisk kilde.
  7. 7. Bibliotek ifølge krav 3, som endvidere omfatter et polynukleotid, der koder for et eller flere polypeptider fra et variabelt domæne af en let kæde.
  8. 8. Bibliotek ifølge krav 7, hvor polypeptideme udtrykkes som IgG’er i fuld. længde.
  9. 9. Polypeptidekspressionsprodukter fra biblioteket ifølge et hvilket som helst af kravene 3-8.
  10. 10. Fremgangsmåde til fremstilling af et antistof af interesse ved at udtrykke biblioteket ifølge et hvilket som helst af kravene 3-8 i en værtscelle.
  11. 11. Bibliotek med vektorer, som indeholder biblioteket ifølge et hvilket som helst af kravene 3-8.
  12. 12. Bibliotek med værtsceller, som indeholder biblioteket med vektorer ifølge krav 11.
  13. 13. Bibliotek med værtsceller ifølge krav 12, hvor værtscellerne er gærceller.
  14. 14. Anvendelse af biblioteket ifølge et hvilket som helst af kravene 3-8 til at isolere et antistof, som binder sig til et antigen.
  15. 15. Kit, som indeholder biblioteket ifølge et hvilket som helst af kravene 3-8.
  16. 16. Bibliotek ifølge krav 7, hvor polypeptideme udtrykkes som intakte antistoffer.
DK11807533.2T 2010-07-16 2011-07-14 Antistofbiblioteker DK2593594T3 (da)

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US36519410P 2010-07-16 2010-07-16
PCT/US2011/044063 WO2012009568A2 (en) 2010-07-16 2011-07-14 Antibody libraries

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US (4) US9354228B2 (da)
EP (4) EP2593594B1 (da)
JP (6) JP6266343B2 (da)
KR (5) KR102024922B1 (da)
CN (2) CN103282560B (da)
AU (4) AU2011279073B2 (da)
BR (1) BR112013001175A2 (da)
CA (3) CA2805875C (da)
DK (3) DK2593594T3 (da)
HK (1) HK1256463A1 (da)
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