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Engineering of a VPAC2 receptor peptide agonist to impart dipeptidyl peptidase IV stability and enhance in vivo glucose disposal.

Authors :
Clairmont KB
Buckholz TM
Pellegrino CM
Buxton JM
Barucci N
Bell A
Ha S
Li F
Claus TH
Salhanick AI
Lumb KJ
Source :
Journal of medicinal chemistry [J Med Chem] 2006 Dec 14; Vol. 49 (25), pp. 7545-8.
Publication Year :
2006

Abstract

VPAC2P-PEG is a VPAC2 receptor agonist peptide that acts as a glucose-dependent insulin secretagogue. Proteolysis by DPPIV may contribute to the in vivo clearance of VPAC2P-PEG. Here, the N-terminus of VPAC2P-PEG is modified by N-terminal acetylation to impart DPPIV resistance. The acetylated peptide, Ac-VPAC2P-PEG, is a selective and potent VPAC2 agonist, resistant to DPPIV proteolysis, and exhibits substantially improved half-life and glucose disposal in rodents. Ac-VPAC2P-PEG has therapeutic potential for diabetes management.

Details

Language :
English
ISSN :
0022-2623
Volume :
49
Issue :
25
Database :
MEDLINE
Journal :
Journal of medicinal chemistry
Publication Type :
Academic Journal
Accession number :
17149884
Full Text :
https://doi.org/10.1021/jm0609059