Literature DB >> 24931377

An inhibition model of BPTI to unlinked dengue virus NS2B-NS3 protease.

Hua Li1, Lei Zhu2, Shulin Hou3, Jing Yang4, Junfeng Wang5, Jinsong Liu6.   

Abstract

One approach to treating the dengue virus infection is to inhibit its NS2B-NS3 protease that plays a vital role in virus maturation. However, the lack of structural information on the active conformation of the protease hindered related drug design. With a co-expression system, we obtained the active two-component protease in its unlinked form. BPTI shows strong competitive inhibitory activity (Ki = 6.5 nM) against this unlinked protease, which adopts a closed conformation. Based on the biochemical and NMR perturbation information, an inhibition model of BPTI to NS2B-NS3 protease is proposed.
Copyright © 2014 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Bovine pancreatic trypsin inhibitor; Closed/active conformation; Dengue virus; NMR spectroscopy; NS2B-NS3 protease

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Year:  2014        PMID: 24931377     DOI: 10.1016/j.febslet.2014.05.063

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  1 in total

1.  A conformational switch high-throughput screening assay and allosteric inhibition of the flavivirus NS2B-NS3 protease.

Authors:  Matthew Brecher; Zhong Li; Binbin Liu; Jing Zhang; Cheri A Koetzner; Adham Alifarag; Susan A Jones; Qishan Lin; Laura D Kramer; Hongmin Li
Journal:  PLoS Pathog       Date:  2017-05-25       Impact factor: 7.464

  1 in total

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