| Literature DB >> 27714789 |
Natalia Gruba1, Jose Ignacio Rodriguez Martinez2, Renata Grzywa3, Magdalena Wysocka1, Marcin Skoreński3, Michał Burmistrz2,4, Maria Łęcka3, Adam Lesner5, Marcin Sieńczyk6, Krzysztof Pyrć7,8.
Abstract
Zika virus (ZIKV), isolated from macaques in Uganda in 1947, was not considered to be a dangerous human pathogen. However, this view has recently changed as ZIKV infections are now associated with serious pathological disorders including microcephaly and Guillain-Barré syndrome. Similar to other viruses in the Flaviviridae family, ZIKV expresses the serine protease NS3 which is responsible for viral protein processing and replication. Herein, we report the expression of an active NS3pro domain fused with the NS2B cofactor (NS2BLN NS3pro ) in a prokaryotic expression system and profile its specificity for synthesized FRET-type substrate libraries. Our findings pave way for screening potential intracellular substrates of NS3 and for developing specific inhibitors of this ZIKV protease.Entities:
Keywords: NS2B-NS3 protease; Zika virus; combinatorial chemistry; substrate library; substrate mapping
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Year: 2016 PMID: 27714789 DOI: 10.1002/1873-3468.12443
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124