کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
5822744 | 1117968 | 2011 | 6 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: Tripeptide inhibitors of dengue and West Nile virus NS2B-NS3 protease Tripeptide inhibitors of dengue and West Nile virus NS2B-NS3 protease](/preview/png/5822744.png)
A series of tripeptide aldehyde inhibitors were synthesized and their inhibitory effect against dengue virus type 2 (DENV2) and West Nile virus (WNV) NS3 protease was evaluated side by side with the aim to discover potent flaviviral protease inhibitors and to examine differences in specificity of the two proteases. The synthesized inhibitors feature a varied N-terminal cap group and side chain modifications of a P2-lysine residue. In general a much stronger inhibitory effect of the tripeptide inhibitors was observed toward WNV protease. The inhibitory concentrations against DENV2 protease were in the micromolar range while they were submicromolar against WNV. The data suggest that a P2-arginine shifts the specificity toward DENV2 protease while WNV protease favors a lysine in the P2 position. Peptides with an extended P2-lysine failed to inhibit DENV2 protease suggesting a size-constrained S2 pocket. Our results generally encourage the investigation of di- and tripeptide aldehydes as inhibitors of DENV and WNV protease.
⺠Tripeptide inhibitors with aldehyde warhead potently inhibit WNV protease but not DENV protease. ⺠DENV2 protease prefers P2-arginine over P2-lysine that is preferred by WNV NS2B-NS3. ⺠Phenylacetyl-KRR-H is the new low micromolar inhibitor of DENV2 protease.
Journal: Antiviral Research - Volume 92, Issue 1, October 2011, Pages 96-101