Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10870139 | FEBS Letters | 2014 | 6 Pages |
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.
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Authors
Hua Li, Lei Zhu, Shulin Hou, Jing Yang, Junfeng Wang, Jinsong Liu,