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MX2021011837A - Método para la generación de una célula que expresa el receptor neonatal de región de fragmento cristalizable (fcrn) mediante la integración dirigida de múltiples casetes de expresión en una organización definida. - Google Patents

Método para la generación de una célula que expresa el receptor neonatal de región de fragmento cristalizable (fcrn) mediante la integración dirigida de múltiples casetes de expresión en una organización definida.

Info

Publication number
MX2021011837A
MX2021011837A MX2021011837A MX2021011837A MX2021011837A MX 2021011837 A MX2021011837 A MX 2021011837A MX 2021011837 A MX2021011837 A MX 2021011837A MX 2021011837 A MX2021011837 A MX 2021011837A MX 2021011837 A MX2021011837 A MX 2021011837A
Authority
MX
Mexico
Prior art keywords
fcrn
expression cassette
cassette encoding
generation
expression cassettes
Prior art date
Application number
MX2021011837A
Other languages
English (en)
Inventor
Stefan Seeber
Tilman Schlothauer
Jasmin Maria Wehrstein
Original Assignee
Hoffmann La Roche
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 Hoffmann La Roche filed Critical Hoffmann La Roche
Publication of MX2021011837A publication Critical patent/MX2021011837A/es

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K14/00Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/705Receptors; Cell surface antigens; Cell surface determinants
    • C07K14/70503Immunoglobulin superfamily
    • C07K14/70535Fc-receptors, e.g. CD16, CD32, CD64 (CD2314/705F)
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D15/00Separating processes involving the treatment of liquids with solid sorbents; Apparatus therefor
    • B01D15/08Selective adsorption, e.g. chromatography
    • B01D15/26Selective adsorption, e.g. chromatography characterised by the separation mechanism
    • B01D15/38Selective adsorption, e.g. chromatography characterised by the separation mechanism involving specific interaction not covered by one or more of groups B01D15/265 and B01D15/30 - B01D15/36, e.g. affinity, ligand exchange or chiral chromatography
    • B01D15/3804Affinity chromatography
    • B01D15/3809Affinity chromatography of the antigen-antibody type, e.g. protein A, G or L chromatography
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K14/00Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/46Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
    • C07K14/47Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K14/00Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/705Receptors; Cell surface antigens; Cell surface determinants
    • C07K14/70503Immunoglobulin superfamily
    • C07K14/70539MHC-molecules, e.g. HLA-molecules
    • 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
    • C12N15/63Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
    • C12N15/79Vectors or expression systems specially adapted for eukaryotic hosts
    • C12N15/85Vectors or expression systems specially adapted for eukaryotic hosts for animal cells
    • 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
    • C12N9/00Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
    • C12N9/93Ligases (6)
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12YENZYMES
    • C12Y603/00Ligases forming carbon-nitrogen bonds (6.3)
    • C12Y603/04Other carbon-nitrogen ligases (6.3.4)
    • C12Y603/04015Biotin-[acetyl-CoA-carboxylase] ligase (6.3.4.15)
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K2319/00Fusion polypeptide
    • C07K2319/20Fusion polypeptide containing a tag with affinity for a non-protein ligand
    • C07K2319/22Fusion polypeptide containing a tag with affinity for a non-protein ligand containing a Strep-tag

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Organic Chemistry (AREA)
  • Genetics & Genomics (AREA)
  • Immunology (AREA)
  • Zoology (AREA)
  • Molecular Biology (AREA)
  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Biophysics (AREA)
  • Medicinal Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Toxicology (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Wood Science & Technology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Cell Biology (AREA)
  • General Engineering & Computer Science (AREA)
  • Biotechnology (AREA)
  • Biomedical Technology (AREA)
  • Microbiology (AREA)
  • Analytical Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Physics & Mathematics (AREA)
  • Plant Pathology (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)

Abstract

En el presente documento se informa de un método para producir el FcRn biotinilado en el extremo C-terminal que comprende los pasos de cultivar una célula de mamífero que comprende un ácido desoxirribonucleico que codifica el FcRn y la ligasa biotina-[acetil-CoA-carboxilasa] (BirA) de E. coli en un medio que contiene biotina, y recuperar el FcRn biotinilado en el extremo C-terminal de la célula o del medio de cultivo, en donde el ácido desoxirribonucleico que codifica el FcRn y la BirA de E. coli está integrado de manera estable en el genoma de la célula de mamífero y comprende en la dirección 5' a 3' un primer casete de expresión que codifica la proteína similar al complejo principal de histocompatibilidad clase I (a-FcRn) que comprende una etiqueta HisAvi en el extremo C-terminal, un segundo casete de expresión que codifica la ß2-microglobulina (ß2m), un tercer casete de expresión que codifica la proteína similar al complejo principal de histocompatibilidad clase I (a-FcRn) que comprende una etiqueta HisAvi en el extremo C-terminal, un cuarto casete de expresión que codifica la ß2-microglobulina (ß2m), y un quinto casete de expresión que codifica la ligasa biotina-[acetil-CoA-car boxilasa] de E.
MX2021011837A 2019-03-29 2020-03-26 Método para la generación de una célula que expresa el receptor neonatal de región de fragmento cristalizable (fcrn) mediante la integración dirigida de múltiples casetes de expresión en una organización definida. MX2021011837A (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP19166030 2019-03-29
PCT/EP2020/058452 WO2020200983A1 (en) 2019-03-29 2020-03-26 Method for the generation of an fcrn expressing cell by targeted integration of multiple expression cassettes in a defined organization

Publications (1)

Publication Number Publication Date
MX2021011837A true MX2021011837A (es) 2021-10-22

Family

ID=66239740

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2021011837A MX2021011837A (es) 2019-03-29 2020-03-26 Método para la generación de una célula que expresa el receptor neonatal de región de fragmento cristalizable (fcrn) mediante la integración dirigida de múltiples casetes de expresión en una organización definida.

Country Status (12)

Country Link
US (1) US20220119482A1 (es)
EP (1) EP3947437A1 (es)
JP (1) JP7250950B2 (es)
KR (1) KR20210134932A (es)
CN (1) CN113661173B (es)
AU (1) AU2020253023B2 (es)
BR (1) BR112021019368A2 (es)
CA (1) CA3130546A1 (es)
IL (1) IL286718A (es)
MX (1) MX2021011837A (es)
SG (1) SG11202109391PA (es)
WO (1) WO2020200983A1 (es)

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU650085B2 (en) 1990-11-13 1994-06-09 Immunex Corporation Bifunctional selectable fusion genes
AU6953394A (en) 1993-05-21 1994-12-20 Targeted Genetics Corporation Bifunctional selectable fusion genes based on the cytosine deaminase (cd) gene
AU2005263331B8 (en) 2004-07-20 2011-06-16 Symphogen A/S Anti-Rhesus D recombinant polyclonal antibody and methods of manufacture
WO2007124452A2 (en) * 2006-04-20 2007-11-01 The Regents Of The University Of California Methods for expressing multiple sirna and shrna from a single vector
US8293533B2 (en) * 2008-12-19 2012-10-23 E.I. Du Pont De Nemours And Company Site-specific integration and stacking of transgenes in soybean via DNA recombinase mediated cassette exchange
WO2013006142A1 (en) 2011-07-05 2013-01-10 Nanyang Technological University A novel process and reagent for rapid genetic alterations in eukaryotic cells
CA2860600C (en) 2012-02-15 2022-07-26 F. Hoffmann-La Roche Ag Fc-receptor based affinity chromatography
AU2014246731A1 (en) * 2013-03-30 2015-11-19 Usha Biotech Limited Methods and constructs for expressing biologically active proteins in mammalian cells
HK1218486A2 (zh) * 2015-12-09 2017-02-17 Ka Lun Alan Ng 提高魚生長的手段和方法
SG11201807881VA (en) * 2016-04-20 2018-10-30 Regeneron Pharma Compositions and methods for making antibodies based on use of an expression-enhancing locus
MX2019010575A (es) 2017-03-10 2019-10-15 Hoffmann La Roche Metodo para producir anticuerpos multiespecificos.
EP3615678B1 (en) * 2017-04-28 2024-07-31 F. Hoffmann-La Roche AG Antibody selection method
CN111886244A (zh) 2017-12-22 2020-11-03 豪夫迈·罗氏有限公司 核酸的靶向整合

Also Published As

Publication number Publication date
JP2022526556A (ja) 2022-05-25
EP3947437A1 (en) 2022-02-09
AU2020253023A1 (en) 2021-09-23
BR112021019368A2 (pt) 2021-12-07
SG11202109391PA (en) 2021-09-29
CA3130546A1 (en) 2020-10-08
AU2020253023B2 (en) 2022-07-14
WO2020200983A1 (en) 2020-10-08
JP7250950B2 (ja) 2023-04-03
CN113661173B (zh) 2024-10-01
KR20210134932A (ko) 2021-11-11
IL286718A (en) 2021-10-31
CN113661173A (zh) 2021-11-16
US20220119482A1 (en) 2022-04-21

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