Advances in Preparation of Peptide and Protein Thioesters Aiming to Use in Medicinal Sciences.

S-cyanylation carboxypeptidase hydrazinolysis native chemical ligation protein semi-synthesis protein thioester

Journal

Chemical & pharmaceutical bulletin
ISSN: 1347-5223
Titre abrégé: Chem Pharm Bull (Tokyo)
Pays: Japan
ID NLM: 0377775

Informations de publication

Date de publication:
2022
Historique:
entrez: 1 5 2022
pubmed: 2 5 2022
medline: 4 5 2022
Statut: ppublish

Résumé

The growing interest in artificial proteins modified by synthetic functional units has fueled the demand for their facile preparation. Native chemical ligation (NCL) enables the chemoselective condensation of peptide thioesters with a cysteine-installed synthetic partner and has enjoyed great success in the production of artificial proteins with up to 100-150 residues. A practical method for converting expressed proteins to the corresponding thioesters should lead to significant progress in the NCL-mediated technology. This account describes our recent contributions to the conversion of naturally occurring peptides to the corresponding thioesters by chemical or chemoenzymatic protocols aiming at their future prevalent use in the preparation of sophisticated protein biologics.

Identifiants

pubmed: 35491186
doi: 10.1248/cpb.c21-01019
doi:

Substances chimiques

Peptides 0
Proteins 0
Sulfur Compounds 0
Cysteine K848JZ4886

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

316-323

Auteurs

Masaya Denda (M)

Institute of Biomedical Sciences and Graduate School of Pharmaceutical Sciences, Tokushima University.

Akira Otaka (A)

Institute of Biomedical Sciences and Graduate School of Pharmaceutical Sciences, Tokushima University.

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Classifications MeSH