Effects of surface water on protein dynamics studied by a novel coarse-grained normal mode approach. Export

@article{citeulike:2647548, abstract = {Normal mode analysis (NMA) has received much attention as a direct approach to extract the collective motions of macromolecules. However, the stringent requirement of computational resources by classical all-atom NMA limits the size of the macromolecules to which the method is normally applied. We implemented a novel coarse-grained normal mode approach based on partitioning the all-atom Hessian matrix into relevant and nonrelevant parts. It is interesting to note that, using classical all-atom NMA results as a reference, we found that this method generates more accurate results than do other coarse-grained approaches, including elastic network model and block normal mode approaches. Moreover, this new method is effective in incorporating the energetic contributions from the nonrelevant atoms, including surface water molecules, into the coarse-grained protein motions. The importance of such improvements is demonstrated by the effect of surface water to shift vibrational modes to higher frequencies and by an increase in overlap of the coarse-grained eigenvector space (the motion directions) with that obtained from molecular dynamics simulations of solvated protein in a water box. These results not only confirm the quality of our method but also point out the importance of incorporating surface structural water in studying protein dynamics.}, address = {Ctr. for Neurobiol. \& Behavior, Columbia University.}, author = {Zhou, L. and Siegelbaum, S. A.}, citeulike-article-id = {2647548}, citeulike-linkout-0 = {http://dx.doi.org/10.1529/biophysj.107.115956}, citeulike-linkout-1 = {http://www.biophysj.org/cgi/content/abstract/94/9/3461}, citeulike-linkout-2 = {http://view.ncbi.nlm.nih.gov/pubmed/18212016}, citeulike-linkout-3 = {http://www.hubmed.org/display.cgi?uids=18212016}, day = {1}, doi = {10.1529/biophysj.107.115956}, issn = {1542-0086}, journal = {Biophysical journal}, keywords = {coarse-grained, solvent-effects}, month = {May}, number = {9}, pages = {3461--3474}, posted-at = {2008-04-10 01:04:40}, priority = {3}, title = {Effects of surface water on protein dynamics studied by a novel coarse-grained normal mode approach.}, url = {http://dx.doi.org/10.1529/biophysj.107.115956}, volume = {94}, year = {2008} }

TY - JOUR ID - citeulike:2647548 L3 - citeulike-article-id:2647548 N2 - Normal mode analysis (NMA) has received much attention as a direct approach to extract the collective motions of macromolecules. However, the stringent requirement of computational resources by classical all-atom NMA limits the size of the macromolecules to which the method is normally applied. We implemented a novel coarse-grained normal mode approach based on partitioning the all-atom Hessian matrix into relevant and nonrelevant parts. It is interesting to note that, using classical all-atom NMA results as a reference, we found that this method generates more accurate results than do other coarse-grained approaches, including elastic network model and block normal mode approaches. Moreover, this new method is effective in incorporating the energetic contributions from the nonrelevant atoms, including surface water molecules, into the coarse-grained protein motions. The importance of such improvements is demonstrated by the effect of surface water to shift vibrational modes to higher frequencies and by an increase in overlap of the coarse-grained eigenvector space (the motion directions) with that obtained from molecular dynamics simulations of solvated protein in a water box. These results not only confirm the quality of our method but also point out the importance of incorporating surface structural water in studying protein dynamics. IS - 9 JF - Biophysical journal SN - 1542-0086 AD - Ctr. for Neurobiol. & Behavior, Columbia University. EP - 3474 TI - Effects of surface water on protein dynamics studied by a novel coarse-grained normal mode approach. VL - 94 SP - 3461 KW - coarse-grained KW - solvent-effects AU - Zhou, L AU - Siegelbaum, SA PY - 2008/05/01/ UR - http://dx.doi.org/10.1529/biophysj.107.115956 ER -