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Peptides conjugated to 2-alkoxy-8-oxo-adenine as potential synthetic vaccines triggering TLR7.

Authors :
Gential GPP
Hogervorst TP
Tondini E
van de Graaff MJ
Overkleeft HS
Codée JDC
van der Marel GA
Ossendorp F
Filippov DV
Source :
Bioorganic & medicinal chemistry letters [Bioorg Med Chem Lett] 2019 Jun 01; Vol. 29 (11), pp. 1340-1344. Date of Electronic Publication: 2019 Mar 30.
Publication Year :
2019

Abstract

Covalent linking of immunogenic oligopeptides with synthetic Toll-like receptor ligands is a useful approach to develop self-adjuvanting vaccines. In particular, small-molecule based agonists of Toll-like receptor 7 (TLR7) that are derived from 8-oxo-adenine core are potentially promising because these chemically robust TLR7 ligands can be connected to peptide T-cell epitopes via straightforward solid-phase peptide synthesis. In this contribution we present the synthesis of a Boc-protected 9-benzyl-2-alkoxy-8-oxo-adenine building block and its application in the online solid phase synthesis of three peptide conjugates that differ in the position of the TLR7 ligand within the peptide. The conjugates are able to induce dendritic cell maturation and T cell proliferation while the position of the ligand impacts T cell proliferation potency.<br /> (Copyright © 2019 The Authors. Published by Elsevier Ltd.. All rights reserved.)

Details

Language :
English
ISSN :
1464-3405
Volume :
29
Issue :
11
Database :
MEDLINE
Journal :
Bioorganic & medicinal chemistry letters
Publication Type :
Academic Journal
Accession number :
30952595
Full Text :
https://doi.org/10.1016/j.bmcl.2019.03.048