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通过对冷冻电镜密度进行建模揭示的Twist诱导的P-SSP7基因组缺陷。

Twist-induced defects of the P-SSP7 genome revealed by modeling the cryo-EM density.

作者信息

Wang Qian, Myers Christopher G, Pettitt B Montgomery

机构信息

†Department of Biochemistry and Molecular Biology, Sealy Center for Structural Biology and Molecular Biophysics, University of Texas Medical Branch, Galveston, Texas 77555-0304, United States.

‡Structural and Computational Biology and Molecular Biophysics Program, Baylor College of Medicine, Houston, Texas 77030, United States.

出版信息

J Phys Chem B. 2015 Apr 16;119(15):4937-43. doi: 10.1021/acs.jpcb.5b00865. Epub 2015 Apr 6.

Abstract

We consider the consequences of assuming that DNA inside of phages can be approximated as a strongly nonlinear persistence length polymer. Recent cryo-EM experiments find a hole in the density map of P-SSP7 phage, located in the DNA segment filling the portal channel of the phage. We use experimentally derived structural constraints with coarse-grained simulation techniques to consider contrasting model interpretations of reconstructed density in the portal channel. The coarse-grained DNA models used are designed to capture the effects of torsional strain and electrostatic environment. Our simulation results are consistent with the interpretation that the vacancy or hole in the experimental density map is due to DNA strain leading to strand separation. We further demonstrate that a moderate negative twisting strain is able to account for the strand separation. This effect of nonlinear persistence length may be important in other aspects of phage DNA packing.

摘要

我们考虑了假设噬菌体内部的DNA可近似为强非线性持久长度聚合物的后果。最近的冷冻电镜实验在P - SSP7噬菌体的密度图中发现了一个空洞,该空洞位于填充噬菌体门户通道的DNA片段中。我们使用实验得出的结构约束和粗粒度模拟技术,来考量对门户通道中重建密度的不同模型解释。所使用的粗粒度DNA模型旨在捕捉扭转应变和静电环境的影响。我们的模拟结果与以下解释一致:实验密度图中的空位或空洞是由于DNA应变导致链分离造成的。我们进一步证明,适度的负扭转应变能够解释链分离现象。这种非线性持久长度的效应在噬菌体DNA包装的其他方面可能很重要。

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