CA2361927A1 - Selection finale d'une evolution dirigee - Google Patents
Selection finale d'une evolution dirigee Download PDFInfo
- Publication number
- CA2361927A1 CA2361927A1 CA002361927A CA2361927A CA2361927A1 CA 2361927 A1 CA2361927 A1 CA 2361927A1 CA 002361927 A CA002361927 A CA 002361927A CA 2361927 A CA2361927 A CA 2361927A CA 2361927 A1 CA2361927 A1 CA 2361927A1
- Authority
- CA
- Canada
- Prior art keywords
- yes
- sequence
- polynucleotide
- progeny
- polynucleotides
- Prior art date
- 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.)
- Abandoned
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
- C12N15/10—Processes for the isolation, preparation or purification of DNA or RNA
- C12N15/1034—Isolating an individual clone by screening libraries
- C12N15/1058—Directional evolution of libraries, e.g. evolution of libraries is achieved by mutagenesis and screening or selection of mixed population of organisms
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
- C12N15/10—Processes for the isolation, preparation or purification of DNA or RNA
- C12N15/102—Mutagenizing nucleic acids
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
- C12N15/10—Processes for the isolation, preparation or purification of DNA or RNA
- C12N15/102—Mutagenizing nucleic acids
- C12N15/1027—Mutagenizing nucleic acids by DNA shuffling, e.g. RSR, STEP, RPR
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
- C12N15/10—Processes for the isolation, preparation or purification of DNA or RNA
- C12N15/1034—Isolating an individual clone by screening libraries
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
- C12N9/14—Hydrolases (3)
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Genetics & Genomics (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Zoology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biomedical Technology (AREA)
- Biotechnology (AREA)
- General Engineering & Computer Science (AREA)
- Microbiology (AREA)
- Molecular Biology (AREA)
- General Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Biophysics (AREA)
- Physics & Mathematics (AREA)
- Crystallography & Structural Chemistry (AREA)
- Plant Pathology (AREA)
- Bioinformatics & Computational Biology (AREA)
- Ecology (AREA)
- Medicinal Chemistry (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
- Enzymes And Modification Thereof (AREA)
- Peptides Or Proteins (AREA)
Abstract
Cette invention concerne des techniques permettant d'obtenir des polynucléotides et des polynucléotides codés en utilisant des techniques non stochastiques d'évolution dirigées (DirectEvolution). La possibilité de récupérer des polynucléotides de pleine longueur issus d'une bibliothèque de molécules d'une lignée générées par mutagenèse présente un avantage particulier dans les techniques fondées sur une sélection finale. Ces techniques comprennent des mutagenèses à saturation de site non stochastiques de polynucléotides (Gene Site Saturation Mutagenesis) et un réassemblage de polynucléotides non stochastique (GeneReassembly). Cette invention concerne des techniques permettant d'obtenir des enzymes aux propriétés physiques et/ou biologiques optimisées. Par l'utilisation de ces techniques de l'invention, on peut faire évoluer des vaccins génétiques, des enzymes, de petites molécules et d'autres molécules qui conviennent vers les propriétés souhaitées. On peut, par exemple, obtenir des vecteurs de vaccin qui font preuve d'une meilleure efficacité lorsqu'on les utilise comme vaccins génétiques. Les vecteurs ainsi obtenus peuvent avoir, par exemple, une expression antigénique renforcée, une absorption dans la cellule améliorée, une meilleure stabilité dans la cellule, une capacité à concevoir une réponse immune et d'autres propriétés de ce genre. Cette invention concerne en outre des techniques permettant d'obtenir diverses molécules biologiques actives, dans le domaine des antibiotiques, des pharmacothérapeutiques, et des caractères transgéniques.
Applications Claiming Priority (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US09/267,118 US6238884B1 (en) | 1995-12-07 | 1999-03-09 | End selection in directed evolution |
US09/267,118 | 1999-03-09 | ||
US09/276,860 US6352842B1 (en) | 1995-12-07 | 1999-03-26 | Exonucease-mediated gene assembly in directed evolution |
US09/276,860 | 1999-06-14 | ||
US09/332,835 US6537776B1 (en) | 1999-06-14 | 1999-06-14 | Synthetic ligation reassembly in directed evolution |
US09/332,835 | 1999-06-14 | ||
PCT/US2000/006497 WO2000053744A2 (fr) | 1999-03-09 | 2000-03-09 | Selection finale d'une evolution dirigee |
Publications (1)
Publication Number | Publication Date |
---|---|
CA2361927A1 true CA2361927A1 (fr) | 2000-09-14 |
Family
ID=27401940
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA002361927A Abandoned CA2361927A1 (fr) | 1999-03-09 | 2000-03-09 | Selection finale d'une evolution dirigee |
Country Status (6)
Country | Link |
---|---|
EP (1) | EP1161529A2 (fr) |
JP (1) | JP2002537836A (fr) |
AU (1) | AU3879300A (fr) |
CA (1) | CA2361927A1 (fr) |
IL (1) | IL145165A0 (fr) |
WO (1) | WO2000053744A2 (fr) |
Families Citing this family (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6537776B1 (en) * | 1999-06-14 | 2003-03-25 | Diversa Corporation | Synthetic ligation reassembly in directed evolution |
US6326204B1 (en) | 1997-01-17 | 2001-12-04 | Maxygen, Inc. | Evolution of whole cells and organisms by recursive sequence recombination |
JP2002526107A (ja) | 1998-10-07 | 2002-08-20 | マキシジェン, インコーポレイテッド | マイコトキシンの解毒のための核酸を生成するためのdnaシャッフリング |
US6368861B1 (en) | 1999-01-19 | 2002-04-09 | Maxygen, Inc. | Oligonucleotide mediated nucleic acid recombination |
IL138206A (en) * | 1999-02-04 | 2011-06-30 | Verenium Corp | Methods for non-stochastic generation of progeny polypeptides and hybrid polynucleotides |
US6531316B1 (en) | 1999-03-05 | 2003-03-11 | Maxyag, Inc. | Encryption of traits using split gene sequences and engineered genetic elements |
US6686515B1 (en) | 1999-11-23 | 2004-02-03 | Maxygen, Inc. | Homologous recombination in plants |
US7094875B2 (en) | 2000-06-23 | 2006-08-22 | Maxygen, Inc. | Co-stimulatory polypeptides |
US6858422B2 (en) | 2000-07-13 | 2005-02-22 | Codexis, Inc. | Lipase genes |
JP2002199890A (ja) * | 2000-10-23 | 2002-07-16 | Inst Of Physical & Chemical Res | 生分解性ポリエステル合成酵素の改変方法 |
US6958217B2 (en) | 2001-01-24 | 2005-10-25 | Genomic Expression Aps | Single-stranded polynucleotide tags |
WO2002059357A2 (fr) * | 2001-01-24 | 2002-08-01 | Genomic Expression Aps | Dosage et kit d'analyse d'expression genique |
US8008459B2 (en) | 2001-01-25 | 2011-08-30 | Evolva Sa | Concatemers of differentially expressed multiple genes |
DK1356037T3 (da) | 2001-01-25 | 2011-06-27 | Evolva Ltd | Bibliotek med en samling af celler |
WO2002092780A2 (fr) * | 2001-05-17 | 2002-11-21 | Diversa Corporation | Nouvelles molecules de liaison a un antigene destinees a des applications therapeutiques, diagnostiques, prophylactiques, enzymatiques, industrielles et agricoles et procedes de generation et de criblage de telles molecules |
WO2004073657A2 (fr) * | 2003-02-19 | 2004-09-02 | Protein Design Labs, Inc. | Methode de diagnostic du cancer, composition et methodes de criblage destinees a identifier des modulateurs du cancer |
EP2374875B1 (fr) | 2006-10-30 | 2015-09-02 | Promega Corporation | Protéines d'hydrolase mutante avec expressions cinétique et fonctionnelle améliorées |
HRP20181319T4 (hr) | 2007-03-30 | 2024-02-16 | The Research Foundation Of The State University Of New York | Oslabljeni virusi koji su korisni kao cjepiva |
EP2980217A1 (fr) * | 2007-12-31 | 2016-02-03 | XOMA Technology Ltd. | Procédés et matériaux pour mutagenèse ciblée |
CN110498822A (zh) * | 2019-09-04 | 2019-11-26 | 上海药明康德新药开发有限公司 | DNA编码化合物库构建中on-DNA芳基叠氮化合物的合成方法 |
Family Cites Families (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5824469A (en) * | 1986-07-17 | 1998-10-20 | University Of Washington | Method for producing novel DNA sequences with biological activity |
EP0285123A3 (fr) * | 1987-04-03 | 1989-02-01 | Stabra AG | Méthode de mutagénèse complète d'acides nucléiques |
EP0527809B1 (fr) * | 1990-04-05 | 1995-08-16 | CREA, Roberto | Mutagenese "traversante" |
US5512463A (en) * | 1991-04-26 | 1996-04-30 | Eli Lilly And Company | Enzymatic inverse polymerase chain reaction library mutagenesis |
US5223408A (en) * | 1991-07-11 | 1993-06-29 | Genentech, Inc. | Method for making variant secreted proteins with altered properties |
US6335160B1 (en) * | 1995-02-17 | 2002-01-01 | Maxygen, Inc. | Methods and compositions for polypeptide engineering |
US6117679A (en) * | 1994-02-17 | 2000-09-12 | Maxygen, Inc. | Methods for generating polynucleotides having desired characteristics by iterative selection and recombination |
US5605793A (en) * | 1994-02-17 | 1997-02-25 | Affymax Technologies N.V. | Methods for in vitro recombination |
US5965408A (en) * | 1996-07-09 | 1999-10-12 | Diversa Corporation | Method of DNA reassembly by interrupting synthesis |
WO1998013487A1 (fr) * | 1996-09-27 | 1998-04-02 | Maxygen, Inc. | Procedes permettant l'optimisation d'une therapie genique grace a un rearrangement et une selection recursifs de sequences |
GB9701425D0 (en) * | 1997-01-24 | 1997-03-12 | Bioinvent Int Ab | A method for in vitro molecular evolution of protein function |
US6153410A (en) * | 1997-03-25 | 2000-11-28 | California Institute Of Technology | Recombination of polynucleotide sequences using random or defined primers |
GB9712512D0 (en) * | 1997-06-16 | 1997-08-20 | Bioinvent Int Ab | A method for in vitro molecular evolution of protein function |
-
2000
- 2000-03-09 EP EP00917887A patent/EP1161529A2/fr not_active Withdrawn
- 2000-03-09 CA CA002361927A patent/CA2361927A1/fr not_active Abandoned
- 2000-03-09 WO PCT/US2000/006497 patent/WO2000053744A2/fr not_active Application Discontinuation
- 2000-03-09 IL IL14516500A patent/IL145165A0/xx unknown
- 2000-03-09 JP JP2000603365A patent/JP2002537836A/ja active Pending
- 2000-03-09 AU AU38793/00A patent/AU3879300A/en not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
EP1161529A2 (fr) | 2001-12-12 |
IL145165A0 (en) | 2002-06-30 |
AU3879300A (en) | 2000-09-28 |
WO2000053744A3 (fr) | 2001-01-18 |
WO2000053744A2 (fr) | 2000-09-14 |
JP2002537836A (ja) | 2002-11-12 |
WO2000053744A9 (fr) | 2001-06-28 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CA2374667C (fr) | Reassemblage synthetique par ligature a evolution dirigee | |
US6773900B2 (en) | End selection in directed evolution | |
US6713282B2 (en) | End selection in directed evolution | |
US6635449B2 (en) | Exonuclease-mediated nucleic acid reassembly in directed evolution | |
US6352842B1 (en) | Exonucease-mediated gene assembly in directed evolution | |
US6696275B2 (en) | End selection in directed evolution | |
AU4039400A (en) | Exonuclease-mediated nucleic acid reassembly in directed evolution | |
CA2361927A1 (fr) | Selection finale d'une evolution dirigee | |
US6939689B2 (en) | Exonuclease-mediated nucleic acid reassembly in directed evolution | |
AU2009212959B2 (en) | Synthetic ligation reassembly in directed evolution | |
US20040023327A1 (en) | End selection in directed evolution | |
AU2005203018A1 (en) | Exonuclease-mediated nucleic acid reassembly in directed evolution | |
Class et al. | Patent application title: SYNTHETIC LIGATION REASSEMBLY IN DIRECTED EVOLUTION Inventors: Jay M. Short (Del Mar, CA, US) | |
AU2005203719A1 (en) | End selection in directed evolution |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
EEER | Examination request | ||
FZDE | Discontinued |