MXPA03011453A - Acetilacion de fragmentos de gp41. - Google Patents

Acetilacion de fragmentos de gp41.

Info

Publication number
MXPA03011453A
MXPA03011453A MXPA03011453A MXPA03011453A MXPA03011453A MX PA03011453 A MXPA03011453 A MX PA03011453A MX PA03011453 A MXPA03011453 A MX PA03011453A MX PA03011453 A MXPA03011453 A MX PA03011453A MX PA03011453 A MXPA03011453 A MX PA03011453A
Authority
MX
Mexico
Prior art keywords
peptide
antifusogenic
fusion
amino acids
host cell
Prior art date
Application number
MXPA03011453A
Other languages
English (en)
Inventor
Tischer Wilhelm
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 MXPA03011453A publication Critical patent/MXPA03011453A/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K19/00Hybrid peptides, i.e. peptides covalently bound to nucleic acids, or non-covalently bound protein-protein complexes
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K14/00Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/005Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from viruses
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • A61P31/14Antivirals for RNA viruses
    • A61P31/18Antivirals for RNA viruses for HIV
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12PFERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P21/00Preparation of peptides or proteins
    • C12P21/02Preparation of peptides or proteins having a known sequence of two or more amino acids, e.g. glutathione
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K2319/00Fusion polypeptide
    • 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
    • C12N2740/00Reverse transcribing RNA viruses
    • C12N2740/00011Details
    • C12N2740/10011Retroviridae
    • C12N2740/15011Lentivirus, not HIV, e.g. FIV, SIV
    • C12N2740/15022New viral proteins or individual genes, new structural or functional aspects of known viral proteins or genes
    • 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
    • C12N2740/00Reverse transcribing RNA viruses
    • C12N2740/00011Details
    • C12N2740/10011Retroviridae
    • C12N2740/16011Human Immunodeficiency Virus, HIV
    • C12N2740/16111Human Immunodeficiency Virus, HIV concerning HIV env
    • C12N2740/16122New viral proteins or individual genes, new structural or functional aspects of known viral proteins or genes

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Biochemistry (AREA)
  • Molecular Biology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Virology (AREA)
  • Genetics & Genomics (AREA)
  • Medicinal Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Zoology (AREA)
  • Wood Science & Technology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Biophysics (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Communicable Diseases (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Biotechnology (AREA)
  • Microbiology (AREA)
  • Oncology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Engineering & Computer Science (AREA)
  • AIDS & HIV (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Peptides Or Proteins (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

La presente invencion se refiere a un proceso para la produccion de un peptido antifusogenico de una longitud de aproximadamente 10 hasta 50 aminoacidos en una celula hospedera procariotica, caracterizado porque, bajo tales condiciones en que los cuerpos de inclusion del peptido antifusogenico o el peptido de fusion son formados, a) en la celula hospedera existe expresado un acido nucleico que codifica el peptido antifusogenico como un peptido diferente del de fusion o que codifica un peptido de fusion de una longitud de aproximadamente 14 hasta 70 aminoacidos que consiste del peptido antifusogenico enlazado N-terminalmente a un peptido adicional de una longitud de aproximadamente 4 hasta 30 aminoacidos; b) la celula hospedera es cultivada; c) los cuerpos de inclusion son recuperados y solubilizados; d) en el caso del peptido de fusion el peptido antifusogenico es retirado por segmentacion del peptido adicional; y e) el peptido antifusogenico es aislado.
MXPA03011453A 2001-06-15 2002-05-27 Acetilacion de fragmentos de gp41. MXPA03011453A (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP01114497 2001-06-15
PCT/EP2002/005782 WO2002103026A2 (en) 2001-06-15 2002-05-27 Method for the recombinant production of peptidic antiviral fusion inhibitors, and acetylation of gb41 fragments

Publications (1)

Publication Number Publication Date
MXPA03011453A true MXPA03011453A (es) 2004-04-05

Family

ID=8177732

Family Applications (1)

Application Number Title Priority Date Filing Date
MXPA03011453A MXPA03011453A (es) 2001-06-15 2002-05-27 Acetilacion de fragmentos de gp41.

Country Status (10)

Country Link
US (2) US6858410B2 (es)
EP (1) EP1402050B1 (es)
JP (1) JP4267444B2 (es)
KR (2) KR100614714B1 (es)
CN (1) CN1255548C (es)
AU (1) AU2002314111A1 (es)
CA (1) CA2450548C (es)
ES (1) ES2525317T3 (es)
MX (1) MXPA03011453A (es)
WO (1) WO2002103026A2 (es)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1255548C (zh) 2001-06-15 2006-05-10 霍夫曼-拉罗奇有限公司 gp41片段的乙酰化
CA2443365C (en) * 2002-11-19 2010-01-12 F. Hoffmann-La Roche Ag Methods for the recombinant production of antifusogenic peptides
JP2007515965A (ja) * 2003-12-23 2007-06-21 セントカー・インコーポレーテツド 抗レトロウイルス性の剤、組成物、方法および用途
WO2007056083A2 (en) * 2005-11-02 2007-05-18 Ambrx, Inc. Biosynthetic polypeptide fusion inhibitors
GB0608368D0 (en) * 2006-04-28 2006-06-07 Isis Innovation Process for making Oligopeptides
TW200817438A (en) * 2006-08-17 2008-04-16 Hoffmann La Roche A conjugate of an antibody against CCR5 and an antifusogenic peptide
US20090143288A1 (en) 2007-03-13 2009-06-04 Roche Palo Alto Llc Peptide-complement conjugates
AU2012362121B2 (en) * 2011-12-29 2017-08-03 Dana-Farber Cancer Institute, Inc. Stabilized antiviral fusion helices
WO2014012090A1 (en) 2012-07-13 2014-01-16 The Broad Institute, Inc. Molecular sleds comprising a positively-charged amino acid sequence and a molecular cargo and uses thereof
CN109069578A (zh) 2016-02-29 2018-12-21 达纳-法伯癌症研究所股份有限公司 用于治疗感染的钉合的细胞内靶向抗微生物肽
US11325955B2 (en) 2017-07-19 2022-05-10 Dana-Farber Cancer Institute, Inc. Stabilized anti-microbial peptides for the treatment of antibiotic-resistant bacterial infections

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US9667A (en) * 1853-04-12 Washiug-machine
US123039A (en) * 1872-01-23 Improvement in canal-boats
DE3034045A1 (de) 1980-09-10 1982-04-22 Boehringer Mannheim Gmbh, 6800 Mannheim Endoproteinase-lys-c aus bakterien, verfahren zu ihrer gewinnung und verwendung
US6936694B1 (en) 1982-05-06 2005-08-30 Intermune, Inc. Manufacture and expression of large structural genes
US4511503A (en) * 1982-12-22 1985-04-16 Genentech, Inc. Purification and activity assurance of precipitated heterologous proteins
US5453363A (en) 1985-10-23 1995-09-26 Boehringer Mannheim Gmbh Process for the activation of t-PA or Ing after genetic expression in prokaryotes
CU22222A1 (es) * 1989-08-03 1995-01-31 Cigb Procedimiento para la expresion de proteinas heterologicas producidas de forma fusionada en escherichia coli, su uso, vectores de expresion y cepas recombinantes
US5595887A (en) 1990-07-16 1997-01-21 Bionebraska, Inc. Purification directed cloning of peptides using carbonic anhydrase as the affinity binding segment
DE69332377T2 (de) 1992-07-13 2003-07-03 Bionebraska, Inc. Verfahren zur modifizierung rekombinanter polypeptide
US5656456A (en) 1992-07-13 1997-08-12 Bionebraska, Inc. Chemical method for selective modification of the N- and/or C-terminal amino acid α-carbon reactive group of a recombinant polypeptide or a portion thereof
WO1994002505A1 (en) 1992-07-20 1994-02-03 Duke University Compounds which inhibit hiv replication
DE69332740T2 (de) * 1992-08-21 2004-02-05 The University Of British Columbia, Vancouver Kationische peptide und verfahren zu deren herstellung
US6017536A (en) 1993-06-07 2000-01-25 Trimeris, Inc. Simian immunodeficiency virus peptides with antifusogenic and antiviral activities
US6479055B1 (en) 1993-06-07 2002-11-12 Trimeris, Inc. Methods for inhibition of membrane fusion-associated events, including respiratory syncytial virus transmission
US5464933A (en) 1993-06-07 1995-11-07 Duke University Synthetic peptide inhibitors of HIV transmission
US5512459A (en) 1993-07-20 1996-04-30 Bionebraska, Inc. Enzymatic method for modification or recombinant polypeptides
US5648244A (en) * 1993-09-27 1997-07-15 President And Fellows Of Harvard College Production, purification, cleavage and use of fusion peptides
DE4405810A1 (de) * 1994-02-23 1995-08-24 Behringwerke Ag Von einem Retrovirus aus der HIV-Gruppe abgeleitete Peptide und deren Verwendung
CA2224008C (en) * 1995-06-07 2009-08-18 Trimeris, Inc. The treatment of hiv and other viral infections using combinatorial therapy
US6846905B2 (en) * 1997-08-15 2005-01-25 Abbott Laboratories Antigen constructs useful in the detection and differentiation of antibodies to HIV
CA2324348C (en) 1998-03-23 2006-03-14 Trimeris, Inc. Methods and compositions for peptide synthesis
US6258782B1 (en) 1998-05-20 2001-07-10 Trimeris, Inc. Hybrid polypeptides with enhanced pharmacokinetic properties
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CN1170932C (zh) * 1998-07-10 2004-10-13 赛欧斯公司 生产等电点高于8或低于5的多肽的方法
WO2000031279A2 (en) 1998-11-20 2000-06-02 Micrologix Biotech Inc. Producing antimicrobial cationic peptides as fusion proteins
EP1149115A4 (en) * 1999-01-08 2005-11-02 Panacos Pharmaceuticals Inc TECHNIQUES FOR ELICITATION OF NEUTRALIZING ANTIBODIES TARGETING HIV-1 gp41
US7582301B1 (en) 1999-05-17 2009-09-01 Conjuchem Biotechnologies, Inc. Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides
ES2296665T3 (es) * 1999-12-16 2008-05-01 Whitehead Institute For Biomedical Research Proteina cinco-helice.
CN1255548C (zh) 2001-06-15 2006-05-10 霍夫曼-拉罗奇有限公司 gp41片段的乙酰化

Also Published As

Publication number Publication date
KR20040010705A (ko) 2004-01-31
WO2002103026A2 (en) 2002-12-27
KR100694919B1 (ko) 2007-03-14
US6858410B2 (en) 2005-02-22
WO2002103026A3 (en) 2003-11-20
US20050058659A1 (en) 2005-03-17
CN1255548C (zh) 2006-05-10
US20030104581A1 (en) 2003-06-05
JP4267444B2 (ja) 2009-05-27
AU2002314111A1 (en) 2003-01-02
KR100614714B1 (ko) 2006-08-21
CA2450548A1 (en) 2002-12-27
US7348423B2 (en) 2008-03-25
CA2450548C (en) 2012-05-01
ES2525317T3 (es) 2014-12-22
KR20060035814A (ko) 2006-04-26
JP2004529660A (ja) 2004-09-30
EP1402050A2 (en) 2004-03-31
EP1402050B1 (en) 2014-10-29
CN1516738A (zh) 2004-07-28

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