Exploring polymorphisms in B-DNA helical conformations

被引:74
作者
Dans, Pablo D. [1 ,2 ]
Perez, Alberto [1 ,3 ,4 ]
Faustino, Ignacio [1 ]
Lavery, Richard [5 ]
Orozco, Modesto [1 ,4 ,6 ]
机构
[1] Inst Res Biomed IRB, Joint IRB BSC Program Computat Biol, Barcelona 08028, Spain
[2] Inst Pasteur Montevideo, Montevideo 11400, Uruguay
[3] SUNY Stony Brook, Laufer Ctr Phys & Quantitat Biol, Stony Brook, NY 11794 USA
[4] Barcelona Supercomp Ctr BSC, Barcelona 08034, Spain
[5] Univ Lyon 1, UMR 5086, CNRS, IBCP, F-69367 Lyon, France
[6] Univ Barcelona, Fac Biol, Dept Bioquim, E-08028 Barcelona, Spain
基金
欧洲研究理事会;
关键词
MOLECULAR-DYNAMICS SIMULATIONS; NUCLEIC-ACIDS; NETWORK MODEL; FORCE-FIELD; BASE-PAIR; DATABASE; FLEXIBILITY; ELASTICITY; ENERGY;
D O I
10.1093/nar/gks884
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The traditional mesoscopic paradigm represents DNA as a series of base-pair steps whose energy response to equilibrium perturbations is elastic, with harmonic oscillations (defining local stiffness) around a single equilibrium conformation. In addition, base sequence effects are often analysed as a succession of independent XpY base-pair steps (i.e. a nearest-neighbour (NN) model with only 10 unique cases). Unfortunately, recent massive simulations carried out by the ABC consortium suggest that the real picture of DNA flexibility may be much more complex. The paradigm of DNA flexibility therefore needs to be revisited. In this article, we explore in detail one of the most obvious violations of the elastic NN model of flexibility: the bimodal distributions of some helical parameters. We perform here an in-depth statistical analysis of a very large set of MD trajectories and also of experimental structures, which lead to very solid evidence of bimodality. We then suggest ways to improve mesoscopic models to account for this deviation from the elastic regime.
引用
收藏
页码:10668 / 10678
页数:11
相关论文
共 38 条
[1]   From rigid base pairs to semiflexible polymers: Coarse-graining DNA [J].
Becker, Nils B. ;
Everaers, Ralf .
PHYSICAL REVIEW E, 2007, 76 (02)
[2]   THE MISSING TERM IN EFFECTIVE PAIR POTENTIALS [J].
BERENDSEN, HJC ;
GRIGERA, JR ;
STRAATSMA, TP .
JOURNAL OF PHYSICAL CHEMISTRY, 1987, 91 (24) :6269-6271
[3]   THE NUCLEIC-ACID DATABASE - A COMPREHENSIVE RELATIONAL DATABASE OF 3-DIMENSIONAL STRUCTURES OF NUCLEIC-ACIDS [J].
BERMAN, HM ;
OLSON, WK ;
BEVERIDGE, DL ;
WESTBROOK, J ;
GELBIN, A ;
DEMENY, T ;
HSIEH, SH ;
SRINIVASAN, AR ;
SCHNEIDER, B .
BIOPHYSICAL JOURNAL, 1992, 63 (03) :751-759
[4]  
Blackburn GM, 2006, NUCLEIC ACIDS IN CHEMISTRY AND BIOLOGY, THIRD EDITION, P383
[5]   The role of dynamic conformational ensembles in biomolecular recognition [J].
Boehr, David D. ;
Nussinov, Ruth ;
Wright, Peter E. .
NATURE CHEMICAL BIOLOGY, 2009, 5 (11) :789-796
[6]   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
[7]   Coarse-grained free energy functions for studying protein conformational changes: A double-well network model [J].
Chu, Jhih-Wei ;
Voth, Gregory A. .
BIOPHYSICAL JOURNAL, 2007, 93 (11) :3860-3871
[8]   Theory of sequence-dependent DNA elasticity [J].
Coleman, BD ;
Olson, WK ;
Swigon, D .
JOURNAL OF CHEMICAL PHYSICS, 2003, 118 (15) :7127-7140
[9]   Molecular simulation of conformational transitions in biomolecules using a combination of structure-based potential and empirical valence bond theory [J].
de Marco, Giuseppe ;
Varnai, Peter .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2009, 11 (45) :10694-10700
[10]   Extracting parameters for base-pair level models of DNA from molecular dynamics simulations [J].
Gonzalez, O ;
Maddocks, JH .
THEORETICAL CHEMISTRY ACCOUNTS, 2001, 106 (1-2) :76-82