Department of Biological Sciences, University of Pittsburgh, Pittsburgh, PA 15260, USA.
J Mol Biol. 2011 Feb 18;406(2):285-312. doi: 10.1016/j.jmb.2010.12.012. Epub 2010 Dec 15.
DNA bending can be promoted by reducing the net negative electrostatic potential around phosphates on one face of the DNA, such that electrostatic repulsion among phosphates on the opposite face drives bending toward the less negative surface. To provide the first assessment of energetic contribution to DNA bending when electrostatic asymmetry is induced by a site-specific DNA binding protein, we manipulated the electrostatics in the EcoRV endonuclease-DNA complex by mutation of cationic side chains that contact DNA phosphates and/or by replacement of a selected phosphate in each strand with uncharged methylphosphonate. Reducing the net negative charge at two symmetrically located phosphates on the concave DNA face contributes -2.3 kcal mol(-1) to -0.9 kcal mol(-1) (depending on position) to complex formation. In contrast, reducing negative charge on the opposing convex face produces a penalty of +1.3 kcal mol(-1). Förster resonance energy transfer experiments show that the extent of axial DNA bending (about 50°) is little affected in modified complexes, implying that modification affects the energetic cost but not the extent of DNA bending. Kinetic studies show that the favorable effects of induced electrostatic asymmetry on equilibrium binding derive primarily from a reduced rate of complex dissociation, suggesting stabilization of the specific complex between protein and markedly bent DNA. A smaller increase in the association rate may suggest that the DNA in the initial encounter complex is mildly bent. The data imply that protein-induced electrostatic asymmetry makes a significant contribution to DNA bending but is not itself sufficient to drive full bending in the specific EcoRV-DNA complex.
DNA 的弯曲可以通过减少 DNA 一侧磷酸基团的净负静电势来促进,使得对面磷酸基团之间的静电排斥作用驱动 DNA 弯曲到负电荷较少的表面。为了首次评估当静电不对称性由特定的 DNA 结合蛋白诱导时对 DNA 弯曲的能量贡献,我们通过突变与 DNA 磷酸基团相互作用的阳离子侧链,或者通过用不带电荷的甲基膦酸酯取代每条链上的选定磷酸基团,来操纵 EcoRV 内切酶-DNA 复合物中的静电。在凹面 DNA 面上两个对称位置的磷酸基团上减少净负电荷会对复合物形成贡献-2.3 kcal/mol 到-0.9 kcal/mol(取决于位置)。相比之下,减少对面凸面的负电荷会产生+1.3 kcal/mol 的惩罚。Förster 共振能量转移实验表明,修饰复合物中轴向 DNA 弯曲的程度(约 50°)几乎没有受到影响,这意味着修饰会影响能量成本但不会影响 DNA 弯曲的程度。动力学研究表明,诱导的静电不对称对平衡结合的有利影响主要来自于复合物解离速率的降低,这表明在蛋白质和明显弯曲的 DNA 之间稳定了特定的复合物。结合速率的较小增加可能表明在初始遭遇复合物中的 DNA 略有弯曲。数据表明,蛋白诱导的静电不对称对 DNA 弯曲有显著贡献,但不足以驱动特定的 EcoRV-DNA 复合物完全弯曲。