Role of conformational fluctuations in the enzymatic reaction of HIV-1 protease. Export

@article{citeulike:1387287, abstract = {The emergence of compensatory drug-resistant mutations in HIV-1 protease challenges the common view of the reaction mechanism of this enzyme. Here, we address this issue by performing classical and ab initio molecular dynamics simulations (MD) on a complex between the enzyme and a peptide substrate. The classical MD calculation reveals large-scale protein motions involving the flaps and the cantilever. These motions modulate the conformational properties of the substrate at the cleavage site. The ab initio calculations show in turn that substrate motion modulates the activation free energy barrier of the enzymatic reaction dramatically. Thus, the catalytic power of the enzyme does not arise from the presence of a pre-organized active site but from the protein mechanical fluctuations. The implications of this finding for the emergence of drug-resistance are discussed.}, address = {Scuola Internazionale Superiore di Studi Avanzati and Istituto Nazionale di Fisica per la Materia, Via Beirut 2-4, 34014 Trieste, Italy.}, author = {Piana, S. and Carloni, P. and Parrinello, M.}, citeulike-article-id = {1387287}, citeulike-linkout-0 = {http://dx.doi.org/10.1016/S0022-2836(02)00301-7}, citeulike-linkout-1 = {http://view.ncbi.nlm.nih.gov/pubmed/12051929}, citeulike-linkout-2 = {http://www.hubmed.org/display.cgi?uids=12051929}, comment = {id : piana2002rcf}, day = {31}, doi = {10.1016/S0022-2836(02)00301-7}, issn = {0022-2836}, journal = {J Mol Biol}, keywords = {clanokinsa, pr, protein}, month = {May}, number = {2}, pages = {567--583}, posted-at = {2007-06-13 13:27:55}, priority = {4}, title = {Role of conformational fluctuations in the enzymatic reaction of HIV-1 protease.}, url = {http://dx.doi.org/10.1016/S0022-2836(02)00301-7}, volume = {319}, year = {2002} }

TY - JOUR ID - citeulike:1387287 L3 - citeulike-article-id:1387287 N2 - The emergence of compensatory drug-resistant mutations in HIV-1 protease challenges the common view of the reaction mechanism of this enzyme. Here, we address this issue by performing classical and ab initio molecular dynamics simulations (MD) on a complex between the enzyme and a peptide substrate. The classical MD calculation reveals large-scale protein motions involving the flaps and the cantilever. These motions modulate the conformational properties of the substrate at the cleavage site. The ab initio calculations show in turn that substrate motion modulates the activation free energy barrier of the enzymatic reaction dramatically. Thus, the catalytic power of the enzyme does not arise from the presence of a pre-organized active site but from the protein mechanical fluctuations. The implications of this finding for the emergence of drug-resistance are discussed. IS - 2 JF - J Mol Biol SN - 0022-2836 AD - Scuola Internazionale Superiore di Studi Avanzati and Istituto Nazionale di Fisica per la Materia, Via Beirut 2-4, 34014 Trieste, Italy. EP - 583 TI - Role of conformational fluctuations in the enzymatic reaction of HIV-1 protease. VL - 319 SP - 567 KW - clanokinsa KW - pr KW - protein N1 - id : piana2002rcf AU - Piana, S AU - Carloni, P AU - Parrinello, M PY - 2002/05/31/ UR - http://dx.doi.org/10.1016/S0022-2836(02)00301-7 ER -