Exploring the versatility of pentafulvene-maleimide cycloaddition as a ligation strategy: buffer and pH effects.
Journal
Organic & biomolecular chemistry
ISSN: 1477-0539
Titre abrégé: Org Biomol Chem
Pays: England
ID NLM: 101154995
Informations de publication
Date de publication:
09 Nov 2022
09 Nov 2022
Historique:
pubmed:
25
10
2022
medline:
11
11
2022
entrez:
24
10
2022
Statut:
epublish
Résumé
Ligation chemistries are often required to perform under stringent conditions that preserve the integrity and function of (bio)conjugates, including specific biological buffers. To explore the versatility of the pentafulvene-maleimide ligation for (bio)conjugations, we studied the stability of the coupling partners and their Diels-Alder cycloaddition (DAC) in buffers used commonly in biological assays, protein chemistry and bioconjugates. The stability of 6,6-dialkylpentafulvene and maleimide derivatives to a panel of buffers with pH values between 3.7 and 10.1 was monitored
Substances chimiques
maleimide
2519R1UGP8
Maleimides
0
Buffers
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM