Chow Edmond, Skolnick Jeffrey
School of Computational Science and Engineering, Georgia Institute of Technology, Atlanta, Georgia.
Center for the Study of Systems Biology, School of Biosciences, Georgia Institute of Technology, Atlanta, Georgia.
Biophys J. 2017 Jun 6;112(11):2261-2270. doi: 10.1016/j.bpj.2017.04.049.
Transcription factors must diffuse through densely packed and coiled DNA to find their binding sites. Using a coarse-grained model of DNA and lac repressor (LacI) in the Escherichia coli nucleoid, simulations were performed to examine how LacI diffuses in such a space. Despite the canonical picture of LacI diffusing rather freely, in reality the DNA is densely packed, is not rigid but highly mobile, and the dynamics of DNA dictates to a great extent the LacI motion. A possibly better picture of unbound LacI motion is that of gated diffusion, where DNA confines LacI in a cage, but LacI can move between cages when hindering DNA strands move out of the way. Three-dimensional diffusion constants for unbound LacI computed from simulations closely match those for unbound LacI in vivo reported in the literature. The internal motions of DNA appear to be governed by strong internal forces arising from being crowded into the small space of the nucleoid. A consequence of the DNA internal motion is that protein target search may be accelerated.
转录因子必须穿过紧密堆积且盘绕的DNA才能找到它们的结合位点。利用大肠杆菌类核中DNA和乳糖阻遏蛋白(LacI)的粗粒度模型,进行了模拟以研究LacI在这样的空间中是如何扩散的。尽管传统观点认为LacI扩散相当自由,但实际上DNA是紧密堆积的,不是刚性的而是高度可移动的,并且DNA的动力学在很大程度上决定了LacI的运动。未结合的LacI运动的一个可能更好的图景是门控扩散,即DNA将LacI限制在一个笼子里,但当阻碍DNA链移开时,LacI可以在笼子之间移动。从模拟中计算出的未结合LacI的三维扩散常数与文献中报道的体内未结合LacI的扩散常数紧密匹配。DNA的内部运动似乎受限于拥挤在类核小空间中产生的强大内力。DNA内部运动的一个结果是蛋白质靶点搜索可能会加速。