| Literature DB >> 24931377 |
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.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