Materials Sciences Research Center, Japan Atomic Energy Agency, Tokai, Ibaraki, Japan; 2 J-PARC Center, Japan Atomic Energy Agency, Tokai, Ibaraki, Japan.
Division of Molecular Life Science, Institute of Advanced Medical Sciences, Tokushima University, Tokushima, Japan.
Biophys J. 2021 Aug 17;120(16):3341-3354. doi: 10.1016/j.bpj.2021.07.001. Epub 2021 Jul 7.
The flexible conformations of a multidomain protein are responsible for its biological functions. Although MurD, a 47-kDa protein that consists of three domains, sequentially changes its domain conformation from an open form to a closed form through a semiclosed form in its enzymatic reaction, the domain dynamics in each conformation remains unclear. In this study, we verify the conformational dynamics of MurD in the corresponding three states (apo and ATP- and inhibitor-bound states) with a combination of small-angle x-ray and neutron scattering (SAXS and SANS), dynamic light scattering (DLS), neutron backscattering (NBS), neutron spin echo (NSE) spectroscopy, and molecular dynamics (MD) simulations. Applying principal component analysis of the MD trajectories, twisting and open-closed domain modes are identified as the major collective coordinates. The deviations of the experimental SAXS profiles from the theoretical calculations based on the known crystal structures become smaller in the ATP-bound state than in the apo state, and a further decrease is evident upon inhibitor binding. These results suggest that domain motions of the protein are suppressed step by step of each ligand binding. The DLS and NBS data yield collective and self-translational diffusion constants, respectively, and we used them to extract collective domain motions in nanometer and nanosecond scales from the NSE data. In the apo state, MurD shows both twisting and open-closed domain modes, whereas an ATP binding suppresses twisting domain motions, and a further reduction of open-closed mode is seen in the inhibitor-binding state. These observations are consistent with the structure modifications measured by the small-angle scattering as well as the MD simulations. Such changes in the domain dynamics associated with the sequential enzymatic reactions should be related to the affinity and reaction efficiency with a ligand that binds specifically to each reaction state.
多结构域蛋白的柔性构象与其生物功能相关。MurD 是一个 47kDa 的蛋白,由三个结构域组成,在其酶促反应中,MurD 通过半闭合构象,依次从开放构象转变为闭合构象。然而,各构象下的结构域动力学仍不清楚。本研究通过小角 X 射线散射(SAXS)和小角中子散射(SANS)、动态光散射(DLS)、背散射中子(NBS)、中子自旋回波(NSE)光谱和分子动力学(MD)模拟相结合,验证了 MurD 在相应三种状态(apo 和 ATP-及抑制剂结合状态)下的构象动力学。通过对 MD 轨迹的主成分分析,确定扭转和开-闭结构域模式为主要的集体坐标。与基于已知晶体结构的理论计算相比,在 ATP 结合状态下,实验 SAXS 图谱的偏离更小,而在抑制剂结合时进一步减小。这些结果表明,随着每个配体的结合,蛋白质的结构域运动逐步受到抑制。DLS 和 NBS 数据分别给出了集体和自扩散常数,我们从 NSE 数据中提取了纳米和纳秒尺度的集体结构域运动。在 apo 状态下,MurD 显示出扭转和开-闭结构域模式,而 ATP 结合抑制了扭转结构域运动,在抑制剂结合状态下,开-闭模式进一步减少。这些观察结果与小角散射以及 MD 模拟所测量的结构修饰一致。与配体结合相关的结构域动力学的变化,应该与特定于每个反应状态的配体的亲和力和反应效率有关。