Bullied no more: when and how DNA shoves proteins around

被引:56
作者
Fogg, Jonathan M. [1 ]
Randall, Graham L. [2 ,3 ]
Pettitt, B. Montgomery [2 ,3 ]
Sumners, De Witt L. [4 ]
Harris, Sarah A. [5 ]
Zechiedrich, Lynn [1 ,2 ]
机构
[1] Baylor Coll Med, Dept Mol Virol & Microbiol, Houston, TX 77030 USA
[2] Baylor Coll Med, Program Struct & Computat Biol & Mol Biophys, Houston, TX 77030 USA
[3] Univ Houston, Dept Chem, Houston, TX 77204 USA
[4] Florida State Univ, Dept Math, Tallahassee, FL 32306 USA
[5] Univ Leeds, Sch Phys & Astron, Leeds LS2 9JT, W Yorkshire, England
基金
美国国家卫生研究院;
关键词
DIFFUSION-DRIVEN MECHANISMS; MOLECULAR-DYNAMICS SIMULATIONS; REPRESSOR-OPERATOR INTERACTION; LOCAL JUXTAPOSITION GEOMETRY; ESCHERICHIA-COLI; CRYSTAL-STRUCTURE; SUPERCOILED DNA; B-DNA; STRUCTURAL TRANSITIONS; II TOPOISOMERASES;
D O I
10.1017/S0033583512000054
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
The predominant protein-centric perspective in protein-DNA-binding studies assumes that the protein drives the interaction. Research focuses on protein structural motifs, electrostatic surfaces and contact potentials, while DNA is often ignored as a passive polymer to be manipulated. Recent studies of DNA topology, the supercoiling, knotting, and linking of the helices, have shown that DNA has the capability to be an active participant in its transactions. DNA topology-induced structural and geometric changes can drive, or at least strongly influence, the interactions between protein and DNA. Deformations of the B-form structure arise from both the considerable elastic energy arising from supercoiling and from the electrostatic energy. Here, we discuss how these energies are harnessed for topology-driven, sequence-specific deformations that can allow DNA to direct its own metabolism.
引用
收藏
页码:257 / 299
页数:43
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