Exploiting the unique features of Zika and Dengue proteases for inhibitor design

0517405 - ÚOCHB 2020 RIV FR eng J - Článek v odborném periodiku
Majerová, Taťána - Novotný, Pavel - Krýsová, Eliška - Konvalinka, Jan
Exploiting the unique features of Zika and Dengue proteases for inhibitor design.
Biochimie. Roč. 166, Nov (2019), s. 132-141. ISSN 0300-9084. E-ISSN 1638-6183
Grant CEP: GA MŠMT LO1302
Institucionální podpora: RVO:61388963
Klíčová slova: active-site inhibitors * allosteric inhibitors * aptamers * precursor * Dengue protease * Zika protease
Obor OECD: Biochemistry and molecular biology
Impakt faktor: 3.413, rok: 2019
Způsob publikování: Omezený přístup
https://www.sciencedirect.com/science/article/abs/pii/S0300908419301439?via%3Dihub

Zika and Dengue viruses have attracted substantial attention from researchers in light of recent outbreaks of Dengue fever and increases in cases of congenital microcephaly in areas with Zika incidence. This review summarizes the current state of knowledge about Zika and Dengue proteases. These enzymes have several interesting features: 1) NS3 serine protease requires the activating co-factor NS2B, which is anchored in the membrane of the endoplasmic reticulum, 2) NS2B displays extensive conformational dynamics, 3) NS3 is a multidomain protein with proteolytic, NTPase, RNA 5' triphosphatase and helicase activity and has many protein-protein interaction partners, 4) NS3 is autoproteolytically released from its precursor. Attempts to design tight-binding and specific active-site inhibitors are complicated by the facts that the substrate pocket of the NS2B-NS3 protease is flat and the active-site ligands are charged. The ionic character of potential active-site inhibitors negatively influences their cell permeability. Possibilities to block cis-autoprocessing of the protease precursor have recently been considered. Additionally, potential allosteric sites on NS2B-NS3 proteases have been identified and allosteric compounds have been designed to impair substrate binding and/or block the NS2B-NS3 interaction. Such compounds could be specific to viral proteases, without off-target effects on host serine proteases, and could have favorable pharmacokinetic profiles. This review discusses various groups of inhibitors of these proteases according to their mechanisms of action and chemical structures.
Trvalý link: http://hdl.handle.net/11104/0302990