DUAL FUNCTION OF ZIKA VIRUS NS2B-NS3 PROTEASE

Abstract

Zika virus (ZIKV) serine protease, indispensable for viral polyprotein processing and replication, is composed of the membrane-anchored NS2B polypeptide and the N-terminal domain of the NS3 polypeptide (NS3pro). The C-terminal domain of the NS3 polypeptide (NS3hel) is necessary for helicase activity and contains an ATP-binding site. We discovered that ZIKV NS2B-NS3pro can bind single-stranded RNA with a Kd of [~]0.3 M, suggesting a novel function. We tested various structural modifications of NS2B-NS3pro and observed that constructs stabilized in the recently discovered "super-open" conformation do not bind RNA. Likewise, stabilization of NS2B-NS3pro in the "closed" (proteolytically active) conformation using substrate inhibitors abolished RNA binding. We posit that RNA binding occurs when ZIKV NS2B-NS3pro adopts the "open" conformation, which we modeled using highly homologous dengue NS2B-NS3pro crystallized in the open conformation. We identified two positively charged fork-like structures present only in the open conformation of NS3pro. These forks are conserved across Flaviviridae family and could be aligned contiguously with the positively charged grove on NS3hel that binds RNA. This led us to propose the "reverse inchworm" model for a tightly intertwined NS2B-NS3 helicase-protease machinery, which suggests that the cycles of NS2B-NS3pro binding and releasing RNA enable the unlimited processivity of NS3hel. The transition to the closed conformation, likely induced by the substrate, enables the classical protease activity of NS2B-NS3pro.