Hierarchical structure of the energy landscape of proteins revisited by time series analysis.I.Mimicking protein dynamics in different time scales

摘要

Time series models,which are constructed from the projections of the molecular-dynamics(MD)runs on principal components(modes),are used to mimic the dynamics of two proteins:tendamistat and immunity protein of colicin E7(ImmE7).Four independent MD runs of tendamistat and three independent runs of ImmE7 protein in vacuum are used to investigate the energy landscapes of these proteins.It is found that mean-square displacements of residues along the modes in different time scales can be mimicked by time series models,which are utilized in dividing protein dynamics into different regimes with respect to the dominating motion type.The first two regimes constitute the dominance of intraminimum motions during the first 5 ps and the random walk motion in a hierarchically higher-level energy minimum,which comprise the initial time period of the trajectories up to 20-40 ps for tendamistat and 80-120 ps for ImmE7.These are also the time ranges within which the linear nonstationary time series are completely satisfactory in explaining protein dynamics.Encountering energy barriers enclosing higher-level energy minima constrains the random walk motion of the proteins,and pseudorelaxation processes at different levels of minima are detected in tendamistat,depending on the sampling window size.Correlation(relaxation)times of 30-40 ps and 150-200 ps are detected for two energy envelopes of successive levels for tendamistat,which gives an overall idea about the hierarchical structure of the energy landscape.However,it should be stressed that correlation times of the modes are highly variable with respect to conformational subspaces and sampling window sizes,indicating the absence of an actual relaxation.The random-walk step sizes and the time length of the second regime are used to illuminate an important difference between the dynamics of the two proteins,which cannot be clarified by the investigation of relaxation times alone:ImmE7 has lower-energy barriers enclosing the higher-level energy minimum,preventing the protein to relax and letting it move in a random-walk fashion for a longer period of time.