Clauvelin Nicolas, Olson Wilma K
Center for Quantitative Biology and Department of Chemistry and Chemical Biology, Rutgers, the State University of New Jersey, Piscataway, New Jersey 08854, United States.
J Phys Chem B. 2021 Mar 11;125(9):2277-2287. doi: 10.1021/acs.jpcb.0c11612. Epub 2021 Feb 26.
The binding of proteins onto DNA contributes to the shaping and packaging of the genome as well as to the expression of specific genetic messages. With a view to understanding the interplay between the presence of proteins and the deformation of DNA involved in such processes, we developed a new method to minimize the elastic energy of DNA fragments at the mesoscale level. Our method makes it possible to obtain the optimal pathways of protein-decorated DNA molecules for which the terminal base pairs are spatially constrained. We focus in this work on the deformations induced by selected architectural proteins on circular DNA. We report the energy landscapes of DNA minicircles subjected to different levels of torsional stress and containing one or two proteins as functions of the chain length and spacing between the proteins. Our results reveal cooperation between the elasticity of the double helix and the structural distortions of DNA induced by bound proteins. We find that the imposed mechanical stress influences the placement of proteins on DNA and that the proteins, in turn, modulate the mechanical stress and thereby broadcast their presence along DNA.
蛋白质与DNA的结合有助于基因组的形成和包装,以及特定遗传信息的表达。为了理解蛋白质的存在与这些过程中涉及的DNA变形之间的相互作用,我们开发了一种新方法,以在中尺度水平上最小化DNA片段的弹性能量。我们的方法能够获得蛋白质修饰的DNA分子的最佳路径,其中末端碱基对在空间上受到限制。在这项工作中,我们专注于选定的结构蛋白对环状DNA诱导的变形。我们报告了承受不同水平扭转应力且包含一两个蛋白质的DNA小环的能量景观,这些景观是链长和蛋白质之间间距的函数。我们的结果揭示了双螺旋弹性与结合蛋白诱导的DNA结构畸变之间的协同作用。我们发现施加的机械应力会影响蛋白质在DNA上的位置,而蛋白质反过来又会调节机械应力,从而沿DNA传播它们的存在。