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
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