Department of Physics and Astronomy, University of California, Irvine, California.
Wenzhou Institute, University of Chinese Academy of Sciences, Wenzhou, China.
Biophys J. 2023 Nov 21;122(22):4476-4487. doi: 10.1016/j.bpj.2023.10.025. Epub 2023 Oct 29.
Transcription factor (TF) proteins regulate gene expression by binding to specific sites on the genome. In the facilitated diffusion model, an optimized search process is achieved by the TF alternating between 3D diffusion in the bulk and 1D diffusion along DNA. While undergoing 1D diffusion, the protein can switch from a search mode for fast diffusion along nonspecific DNA to a recognition mode for stable binding to specific DNA. It was recently noticed that, for a small TF domain protein, reorientations on DNA happen between the nonspecific and specific DNA binding. We here conducted all-atom molecular dynamics simulations with steering forces to reveal the protein-DNA binding free energetics, confirming that the search and recognition modes are distinguished primarily by protein orientations on the DNA. As the binding free energy difference between the specific and nonspecific DNA system slightly deviates from that being estimated directly from dissociation constants on 15-bp DNA constructs, we hypothesize that the discrepancy can come from DNA sequences flanking the 6-bp central binding sites that impact on the dissociation kinetics measurements. The hypothesis is supported by a simplified spherical protein-DNA model along with stochastic simulations and kinetic modeling.
转录因子 (TF) 蛋白通过结合基因组上的特定位点来调节基因表达。在易化扩散模型中,TF 通过在主体中进行 3D 扩散和沿着 DNA 的 1D 扩散之间交替,实现了优化的搜索过程。在进行 1D 扩散时,该蛋白可以从快速扩散到非特异性 DNA 的搜索模式切换到稳定结合特异性 DNA 的识别模式。最近有人注意到,对于一个小的 TF 结构域蛋白,在非特异性和特异性 DNA 结合之间会发生 DNA 上的重新取向。我们在这里进行了带有导向力的全原子分子动力学模拟,以揭示蛋白-DNA 结合的自由能,证实搜索和识别模式主要由 DNA 上的蛋白取向区分。由于特异性和非特异性 DNA 系统之间的结合自由能差异与直接从 15 个碱基对 DNA 构建体上的解离常数估计的差异略有偏离,我们假设这种差异可能来自于影响解离动力学测量的中央结合位点 6 个碱基对侧翼的 DNA 序列。该假设得到了简化的球形蛋白-DNA 模型以及随机模拟和动力学建模的支持。