Department of Biochemistry and Molecular Biology, Sealy Center for Structural Biology and Molecular Biophysics, University of Texas Medical Branch , Galveston, Texas 77555-1068, United States.
J Phys Chem B. 2017 Oct 19;121(41):9548-9556. doi: 10.1021/acs.jpcb.7b07779. Epub 2017 Oct 4.
In the target DNA search process, sequence-specific DNA-binding proteins first nonspecifically bind to DNA and stochastically move from one site to another before reaching their targets. To rigorously assess how the translocation process influences NMR signals from proteins interacting with nonspecific DNA, we incorporated a discrete-state kinetic model for protein translocation on DNA into the McConnell equation. Using this equation, we simulated line shapes of NMR signals from proteins undergoing translocations on DNA through sliding, dissociation/reassociation, and intersegment transfer. Through this analysis, we validated an existing NMR approach for kinetic investigations of protein translocation on DNA, which utilizes NMR line shapes of two nonspecific DNA-protein complexes and their mixture. We found that, despite its use of simplistic two-state approximation neglecting the presence of many microscopic states, the previously proposed NMR approach provides accurate kinetic information on the intermolecular translocations of proteins between two DNA molecules. Interestingly, our results suggest that the same NMR approach can also provide qualitative information about the one-dimensional diffusion coefficient for proteins sliding on DNA.
在目标 DNA 搜索过程中,序列特异性 DNA 结合蛋白首先非特异性地与 DNA 结合,并在到达其靶标之前随机从一个位置移动到另一个位置。为了严格评估易位过程如何影响与非特异性 DNA 相互作用的蛋白质的 NMR 信号,我们将 DNA 上蛋白质易位的离散状态动力学模型纳入 McConnell 方程。使用该方程,我们模拟了通过滑动、解离/再结合和片段间转移在 DNA 上易位的蛋白质的 NMR 信号的线形状。通过这种分析,我们验证了一种现有的用于研究 DNA 上蛋白质易位的动力学的 NMR 方法,该方法利用了两个非特异性 DNA-蛋白质复合物及其混合物的 NMR 线形状。我们发现,尽管它使用了忽略许多微观状态的简单两态近似,但先前提出的 NMR 方法可提供关于两个 DNA 分子之间蛋白质分子间易位的准确动力学信息。有趣的是,我们的结果表明,相同的 NMR 方法还可以提供有关在 DNA 上滑动的蛋白质的一维扩散系数的定性信息。