Literature DB >> 17149884

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

Kevin B Clairmont1, Thomas M Buckholz, Carla M Pellegrino, Joanne M Buxton, Nicole Barucci, Andrea Bell, Sha Ha, Fugang Li, Thomas H Claus, Arthur I Salhanick, Kevin J Lumb.   

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.

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Year:  2006        PMID: 17149884     DOI: 10.1021/jm0609059

Source DB:  PubMed          Journal:  J Med Chem        ISSN: 0022-2623            Impact factor:   7.446


  2 in total

1.  Salinity-induced regulation of the myo-inositol biosynthesis pathway in tilapia gill epithelium.

Authors:  Romina Sacchi; Johnathon Li; Fernando Villarreal; Alison M Gardell; Dietmar Kültz
Journal:  J Exp Biol       Date:  2013-09-26       Impact factor: 3.312

2.  Structural definition and substrate specificity of the S28 protease family: the crystal structure of human prolylcarboxypeptidase.

Authors:  Stephen M Soisson; Sangita B Patel; Pravien D Abeywickrema; Noel J Byrne; Ronald E Diehl; Dawn L Hall; Rachael E Ford; John C Reid; Keith W Rickert; Jennifer M Shipman; Sujata Sharma; Kevin J Lumb
Journal:  BMC Struct Biol       Date:  2010-06-11
  2 in total

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