Hepatitis C virus helicase is a molecular motor that splits duplex DNA while actively moving over it. An approximate coarse-grained dynamical description of this protein, including its interactions with DNA and ATP, is constructed. Using such a mechanical model, entire operation cycles of an important protein machine could be followed in structurally resolved dynamical simulations. Ratcheting inchworm translocation and spring-loaded DNA unwinding, suggested by experimental data, were reproduced. Thus, feasibility of coarse-grained simulations, bridging a gap between full molecular dynamics and reduced phenomenological theories of molecular motors, has been demonstrated. molecular machines | elastic-network models | conformational relaxation | mechanochemical motions | nonequilibrium dynamics P rotein machines and, particularly, molecular motors are of fundamental importance for biological cells. Underlying their organized activity are ordered conformational motions driven in proteins by ATP hydrolysis (1). Such cyclic motions are on the scales of milliseconds and thus are too slow to be followed in molecular dynamics (MD) simulations. On the other hand, simple physical modeling in terms of stochastic automata, oscillators, or Brownian ratchets lacks conformational aspects of protein dynamics (2-4). Coarse-grained models of molecular motors, which allow structurally resolved dynamical simulations of entire operation cycles, are therefore needed.In the last decade, coarse-grained descriptions of proteins, based on elastic-network models (ENM), have been proposed and investigated (5-9). In such models, each residue is usually considered as a single particle. The particles interact via elastic potentials, introduced in such a way that the minimum of elastic energy for a network is reached for a configuration coinciding with the known equilibrium conformation of the considered protein. Despite their high simplicity, ENM are able to correctly predict conformational changes induced by ligand binding. Such network models have also been used to describe conformational relaxation (10, 11) and functional mechanochemical motions in motor proteins (10, 12). Moreover, coarse-grained descriptions of DNA molecules, modeling them as semiflexible elastic polymers, are broadly used (13-15). Here, we show that entire operation cycles of a protein motor, involving its interactions with DNA, can be computationally traced by combining the elastic-network relaxation description for a protein with the elastic polymer description for DNA.Hepatitis C virus (HCV) helicase is a motor protein that, translocating itself, unwinds duplex RNA or DNA (see review in ref. 16). Experimental and theoretical investigations of this motor, representative for a broad class of helicases (17), have been performed (18)(19)(20)(21)(22)(23)(24)(25)(26)(27). Experimental data suggest that ratcheting inchworm translocation (19,27,28) and spring-loaded DNA unwinding (26) constitute the principal mechanism of its operation. The elasticnetwork description for HCV ...