ATP dependent NS3 helicase interaction with RNA: insights from molecular simulations

作者：Perez Villa Andrea; Darvas Maria; Bussi Giovanni^*

来源：Nucleic Acids Research, 2015, 43(18): 8725-8734.

DOI：10.1093/nar/gkv872

Non-structural protein 3 (NS3) helicase fromhepatitis C virus is an enzyme that unwinds and translocates along nucleic acids with an ATP-dependent mechanism and has a key role in the replication of the viral RNA. An inchworm-like mechanism for translocation has been proposed based on crystal structures and single molecule experiments. We here perform atomistic molecular dynamics in explicit solvent on the microsecond time scale of the available experimental structures. We also construct and simulate putative intermediates for the translocation process, and we perform non-equilibrium targeted simulations to estimate their relative stability. For each of the simulated structures we carefully characterize the available conformational space, the ligand binding pocket, and the RNA binding cleft. The analysis of the hydrogen bond network and of the non-equilibrium trajectories indicates an ATP-dependent stabilization of one of the protein conformers. Additionally, enthalpy calculations suggest that entropic effects might be crucial for the stabilization of the experimentally observed structures.

• 出版日期2015-10-15