Department of Chemistry, Center for Drug Discovery, Design, and Delivery(CD4), Center for Scientific Computation, Southern Methodist University, Dallas, Texas 75275, United States of America.
Sci Rep. 2017 Apr 20;7:46626. doi: 10.1038/srep46626.
VIVID(VVD) protein is a Light-Oxygen-Voltage(LOV) domain in circadian clock system. Upon blue light activation, a covalent bond is formed between VVD residue Cys108 and its cofactor flavin adenine dinucleotide(FAD), and prompts VVD switching from Dark state to Light state with significant conformational deviation. However, the mechanism of this local environment initiated global protein conformational change remains elusive. We employed a recently developed computational approach, rigid residue scan(RRS), to systematically probe the impact of the internal degrees of freedom in each amino acid residue of VVD on its overall dynamics by applying rigid body constraint on each residue in molecular dynamics simulations. Key residues were identified with distinctive impacts on Dark and Light states, respectively. All the simulations display wide range of distribution on a two-dimensional(2D) plot upon structural root-mean-square deviations(RMSD) from either Dark or Light state. Clustering analysis of the 2D RMSD distribution leads to 15 representative structures with drastically different conformation of N-terminus, which is also a key difference between Dark and Light states of VVD. Further principle component analyses(PCA) of RRS simulations agree with the observation of distinctive impact from individual residues on Dark and Light states.
VIVID(VVD)蛋白是生物钟系统中的一个光氧电压(LOV)结构域。在蓝光激活后,VVD 残基半胱氨酸 108 与辅因子黄素腺嘌呤二核苷酸(FAD)之间形成共价键,促使 VVD 从暗状态切换到亮状态,构象明显偏离。然而,这种局部环境引发的全局蛋白质构象变化的机制仍然难以捉摸。我们采用了最近开发的计算方法——刚性残基扫描(RRS),通过在分子动力学模拟中对每个残基施加刚体约束,系统地探测 VVD 中每个氨基酸残基的内部自由度对其整体动力学的影响。确定了对暗态和亮态分别具有独特影响的关键残基。所有模拟在结构均方根偏差(RMSD)偏离暗态或亮态的二维(2D)图谱上显示出广泛的分布。对 2D RMSD 分布的聚类分析产生了 15 个具有截然不同的 N 端构象的代表性结构,这也是 VVD 暗态和亮态之间的关键区别。进一步对 RRS 模拟的主成分分析(PCA)也与单个残基对暗态和亮态的独特影响的观察结果一致。