Dynamics of B-DNA on the microsecond time scale

被引:209
作者
Perez, Alberto
Luque, F. Javier
Orozco, Modesto
机构
[1] Inst Nacl Bioinformat Parc Cient Barcelona, Inst Rec Biomed, Barcelona 08028, Spain
[2] Barcelona Supercomp Ctr, Computat Biol Program, Barcelona 08028, Spain
[3] Fac Farm, Dept Fisicoquim, Barcelona 08028, Spain
[4] Fac Biol, Dept Bioquim, Barcelona 08028, Spain
关键词
D O I
10.1021/ja0753546
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We present the first microsecond MD simulation of B-DNA. Trajectory shows good agreement with available data and clarifies the mu s dynamics of DNA. The duplex is sampling the B-conformation, but many relevant local transitions are found, including S -> N repuckers (up to 7 N-sugars are found simultaneously), local B-II transitions (15% of the dinucleotides are in B-II-form; some of these forms are stable for up to 7 ns), and sequence-dependent alpha/gamma transitions (happening in the 7-50 ns time scale, and being stable for up to 80 ns). Partial and total openings are often detected, but no base flipping is found. A-T openings happen after amplification of propeller twist movements, while G-C pairs (which can be opened for up to 1 ns) are opened by a complex mechanism which is often catalyzed by cations. A high affinity Na+ binding site is found in the center of the minor groove. Access to this site by cations is difficult (average entry time 400 ns), but once inside, the ion remains for long periods of time (10-15 ns), producing a sizable narrowing of the minor groove. The essential dynamics of DNA fits well with the pattern of deformation needed to (i) sample uncommon right-handed forms and (ii) sample conformations adopted by DNA when bound to proteins. Clearly, DNA has evolved to be not only a stable structure able to maintain and transmit the genetic information but also a flexible entity whose intrinsic pattern of deformability matches its functional needs.
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收藏
页码:14739 / 14745
页数:7
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[1]   ESSENTIAL DYNAMICS OF PROTEINS [J].
AMADEI, A ;
LINSSEN, ABM ;
BERENDSEN, HJC .
PROTEINS-STRUCTURE FUNCTION AND GENETICS, 1993, 17 (04) :412-425
[2]   On the calculation of entropy from covariance matrices of the atomic fluctuations [J].
Andricioaei, I ;
Karplus, M .
JOURNAL OF CHEMICAL PHYSICS, 2001, 115 (14) :6289-6292
[3]   Flexibility of the B-DNA backbone: effects of local and neighbouring sequences on pyrimidine-purine steps [J].
Bertrand, HO ;
Ha-Duong, T ;
Fermandjian, S ;
Hartmann, B .
NUCLEIC ACIDS RESEARCH, 1998, 26 (05) :1261-1267
[4]   Nucleic acids: theory and computer simulation, Y2K [J].
Beveridge, DL ;
McConnell, KJ .
CURRENT OPINION IN STRUCTURAL BIOLOGY, 2000, 10 (02) :182-196
[5]   Molecular dynamics simulations of the 136 unique tetranucleotide sequences of DNA oligonucleotides.: I.: Research design and results on d(CpG) steps [J].
Beveridge, DL ;
Barreiro, G ;
Byun, KS ;
Case, DA ;
Cheatham, TE ;
Dixit, SB ;
Giudice, E ;
Lankas, F ;
Lavery, R ;
Maddocks, JH ;
Osman, R ;
Seibert, E ;
Sklenar, H ;
Stoll, G ;
Thayer, KM ;
Varnai, P ;
Young, MA .
BIOPHYSICAL JOURNAL, 2004, 87 (06) :3799-3813
[6]   The Amber biomolecular simulation programs [J].
Case, DA ;
Cheatham, TE ;
Darden, T ;
Gohlke, H ;
Luo, R ;
Merz, KM ;
Onufriev, A ;
Simmerling, C ;
Wang, B ;
Woods, RJ .
JOURNAL OF COMPUTATIONAL CHEMISTRY, 2005, 26 (16) :1668-1688
[7]   Simulation and modeling of nucleic acid structure, dynamics and interactions [J].
Cheatham, TE .
CURRENT OPINION IN STRUCTURAL BIOLOGY, 2004, 14 (03) :360-367
[8]   A modified version of the Cornell et al. force field with improved sugar pucker phases and helical repeat [J].
Cheatham, TE ;
Cieplak, P ;
Kollman, PA .
JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS, 1999, 16 (04) :845-862
[9]   MOLECULAR-DYNAMICS SIMULATIONS ON SOLVATED BIOMOLECULAR SYSTEMS - THE PARTICLE MESH EWALD METHOD LEADS TO STABLE TRAJECTORIES OF DNA, RNA, AND PROTEINS [J].
CHEATHAM, TE ;
MILLER, JL ;
FOX, T ;
DARDEN, TA ;
KOLLMAN, PA .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1995, 117 (14) :4193-4194
[10]  
Cheatham TE, 2001, BIOPOLYMERS, V56, P232