Are many-body effects important in protein folding?

被引:64
作者
van der Vaart, A
Bursulaya, BD
Brooks, CL
Merz, KM
机构
[1] Penn State Univ, Dept Chem, University Pk, PA 16802 USA
[2] Scripps Res Inst, Res Inst, Dept Mol Biol, La Jolla, CA 92037 USA
关键词
D O I
10.1021/jp001193f
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In this article we investigate the importance of many-body and nonclassical effects, such as polarization and charge transfer, on the folding of the betanova protein. Our calculations show that these effects are crucial in stabilization of the system. Moreover, both polarization and charge transfer significantly alter the charge distribution of the system. Our detailed study shows that these fluctuations in charge are solely dependent on the local environment and not on the overall fold of the protein. Moreover, the contributions of polarization and charge transfer are roughly constant during the protein folding process. This means that the folding driving force is largely determined by the electrostatic energy. Our findings indicate that the folding of betanova can be accurately described by effective two-body potentials, despite the absence of explicit polarization and charge transfer in these models.
引用
收藏
页码:9554 / 9563
页数:10
相关论文
共 54 条
[1]  
Allen M. P., 1987, COMPUTER SIMULATIONS, DOI [10.1093/oso/9780198803195.001.0001, DOI 10.1093/OSO/9780198803195.001.0001]
[2]   ATOM DIPOLE INTERACTION MODEL FOR MOLECULAR POLARIZABILITY - APPLICATION TO POLYATOMIC-MOLECULES AND DETERMINATION OF ATOM POLARIZABILITIES [J].
APPLEQUIST, J ;
CARL, JR ;
FUNG, KK .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1972, 94 (09) :2952-+
[3]   Adaptive umbrella sampling of the potential energy: modified updating procedure of the umbrella potential and application to peptide folding [J].
Bartels, C ;
Schaefer, M ;
Karplus, M .
THEORETICAL CHEMISTRY ACCOUNTS, 1999, 101 (1-3) :62-66
[4]   FIRST-PRINCIPLES CALCULATION OF THE FOLDING FREE-ENERGY OF A 3-HELIX BUNDLE PROTEIN [J].
BOCZKO, EM ;
BROOKS, CL .
SCIENCE, 1995, 269 (5222) :393-396
[5]   CHARMM - A PROGRAM FOR MACROMOLECULAR ENERGY, MINIMIZATION, AND DYNAMICS CALCULATIONS [J].
BROOKS, BR ;
BRUCCOLERI, RE ;
OLAFSON, BD ;
STATES, DJ ;
SWAMINATHAN, S ;
KARPLUS, M .
JOURNAL OF COMPUTATIONAL CHEMISTRY, 1983, 4 (02) :187-217
[6]   Folding free energy surface of a three-stranded β-sheet protein [J].
Bursulaya, BD ;
Brooks, CL .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1999, 121 (43) :9947-9951
[7]   IMPLEMENTATION OF NONADDITIVE INTERMOLECULAR POTENTIALS BY USE OF MOLECULAR-DYNAMICS - DEVELOPMENT OF A WATER WATER POTENTIAL AND WATER ION CLUSTER INTERACTIONS [J].
CALDWELL, J ;
DANG, LX ;
KOLLMAN, PA .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1990, 112 (25) :9144-9147
[8]   Folding and translocation of the undecamer of poly-L-leucine across the water-hexane interface. A molecular dynamics study [J].
Chipot, C ;
Pohorille, A .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1998, 120 (46) :11912-11924
[9]   A 2ND GENERATION FORCE-FIELD FOR THE SIMULATION OF PROTEINS, NUCLEIC-ACIDS, AND ORGANIC-MOLECULES [J].
CORNELL, WD ;
CIEPLAK, P ;
BAYLY, CI ;
GOULD, IR ;
MERZ, KM ;
FERGUSON, DM ;
SPELLMEYER, DC ;
FOX, T ;
CALDWELL, JW ;
KOLLMAN, PA .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1995, 117 (19) :5179-5197
[10]   Hydrogen bonds: a comparison of semiempirical and ab initio treatments [J].
Dannenberg, JJ .
JOURNAL OF MOLECULAR STRUCTURE-THEOCHEM, 1997, 401 (03) :279-286