Synthetic Neoglycoconjugates of Hepta- and Nonamannoside Ligands for Eliciting Oligomannose-Specific HIV-1-Neutralizing Antibodies.
HIV/AIDS
glycoconjugates
glycosylation
oligomannosides
synthesis
Journal
Chembiochem : a European journal of chemical biology
ISSN: 1439-7633
Titre abrégé: Chembiochem
Pays: Germany
ID NLM: 100937360
Informations de publication
Date de publication:
05 04 2022
05 04 2022
Historique:
revised:
01
02
2022
received:
28
01
2022
pubmed:
2
2
2022
medline:
8
4
2022
entrez:
1
2
2022
Statut:
ppublish
Résumé
Oligomannose-type glycans on the spike protein of HIV-1 constitute relevant epitopes to elicit broadly neutralizing antibodies (bnAbs). Herein we describe an improved synthesis of α- and β-linked hepta- and nonamannosyl ligands that were subsequently converted into BSA and CRM
Identifiants
pubmed: 35104013
doi: 10.1002/cbic.202200061
pmc: PMC9108342
mid: NIHMS1801167
doi:
Substances chimiques
Antibodies, Neutralizing
0
Epitopes
0
HIV Antibodies
0
Ligands
0
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
e202200061Subventions
Organisme : NIAID NIH HHS
ID : R01 AI134299
Pays : United States
Informations de copyright
© 2022 The Authors. ChemBioChem published by Wiley-VCH GmbH.
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