| Literature DB >> 27241372 |
Melgious J Y Ang1, Huichang A Lim1, Anders Poulsen1, John Liang Kuan Wee1, Fui Mee Ng1, Joma Joy1, Jeffrey Hill1, C S Brian Chia1.
Abstract
The mosquito-borne West Nile virus (WNV) causes a wide range of symptoms ranging from fever to the often fatal viral encephalitis. To date, no vaccine or drug therapy is available. The trypsin-like WNV NS2B-NS3 protease is deemed a plausible drug target and was shown to be inhibited by bovine pancreatic trypsin inhibitor (BPTI), a 58-residue protein isolated from bovine lung. Herein, we report a protein truncation study that resulted in a novel 14-residue cyclic peptide with equipotent inhibitory activity to native BPTI. We believe our truncation strategy can be further applied in the development of peptide-based inhibitors targeting trypsin-like proteases.Entities:
Keywords: Aprotinin; BPTI; NS3 protease; West Nile virus; peptide
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Year: 2016 PMID: 27241372 DOI: 10.1080/14756366.2016.1190713
Source DB: PubMed Journal: J Enzyme Inhib Med Chem ISSN: 1475-6366 Impact factor: 5.051