FR2419278A1 - Procede de synthese de chaines peptidiques - Google Patents

Procede de synthese de chaines peptidiques

Info

Publication number
FR2419278A1
FR2419278A1 FR7807016A FR7807016A FR2419278A1 FR 2419278 A1 FR2419278 A1 FR 2419278A1 FR 7807016 A FR7807016 A FR 7807016A FR 7807016 A FR7807016 A FR 7807016A FR 2419278 A1 FR2419278 A1 FR 2419278A1
Authority
FR
France
Prior art keywords
complex
reacted
precursor
polynucleotide
acid
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.)
Granted
Application number
FR7807016A
Other languages
English (en)
Other versions
FR2419278B1 (fr
Inventor
Garfield Paul Royer
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Pierce Chemical Co
Original Assignee
Pierce Chemical Co
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 Pierce Chemical Co filed Critical Pierce Chemical Co
Priority to FR7807016A priority Critical patent/FR2419278A1/fr
Publication of FR2419278A1 publication Critical patent/FR2419278A1/fr
Application granted granted Critical
Publication of FR2419278B1 publication Critical patent/FR2419278B1/fr
Granted legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/08—Tripeptides
    • C07K5/0802—Tripeptides with the first amino acid being neutral
    • C07K5/0804—Tripeptides with the first amino acid being neutral and aliphatic
    • C07K5/0808—Tripeptides with the first amino acid being neutral and aliphatic the side chain containing 2 to 4 carbon atoms, e.g. Val, Ile, Leu
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K1/00—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
    • C07K1/04—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length on carriers
    • C07K1/042—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length on carriers characterised by the nature of the carrier

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Genetics & Genomics (AREA)
  • Biochemistry (AREA)
  • Biophysics (AREA)
  • General Health & Medical Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Molecular Biology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Analytical Chemistry (AREA)
  • Peptides Or Proteins (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)

Abstract

L'invention concerne un procédé amélioré de synthèse d'une chaîne peptidique. On fait réagir en solution aqueuse un complexe précurseur d'amino-acide contenant un groupement alpha -amino ou carboxy bloqué et un polynucléotide porteur avec un second segment amino-acide ; on sépare le complexe ayant réagi de l'acide n'ayant pas réagi en copulant de façon réversible le polynucléotide du complexe à un polynucléotide adsorbant complémentaire immobilisé sur un support insoluble et on élue le complexe du support sous forme d'une solution aqueuse On débloque par voie enzymatique le complexe et on l'utilise comme précurseur pour répéter la réaction avec un autre acide, et ainsi de suite jusqu'à ce qu'on ait fixé au précurseur le nombre d'acides désiré. De préférence, au cours du procédé, on enlève par dégradation enzymatique les chaînes qui n'ont pas réagi avec un acide donné. Ce procédé permet d'obtenir de façon sûre des chaînes peptidiques de poids moléculaire élevé correspondant réellement à la chaîne peptidique désirée.
FR7807016A 1978-03-10 1978-03-10 Procede de synthese de chaines peptidiques Granted FR2419278A1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
FR7807016A FR2419278A1 (fr) 1978-03-10 1978-03-10 Procede de synthese de chaines peptidiques

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR7807016A FR2419278A1 (fr) 1978-03-10 1978-03-10 Procede de synthese de chaines peptidiques

Publications (2)

Publication Number Publication Date
FR2419278A1 true FR2419278A1 (fr) 1979-10-05
FR2419278B1 FR2419278B1 (fr) 1981-05-29

Family

ID=9205640

Family Applications (1)

Application Number Title Priority Date Filing Date
FR7807016A Granted FR2419278A1 (fr) 1978-03-10 1978-03-10 Procede de synthese de chaines peptidiques

Country Status (1)

Country Link
FR (1) FR2419278A1 (fr)

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2108520A5 (fr) * 1970-09-26 1972-05-19 Hoffmann La Roche

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2108520A5 (fr) * 1970-09-26 1972-05-19 Hoffmann La Roche

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
CA1977 *

Also Published As

Publication number Publication date
FR2419278B1 (fr) 1981-05-29

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