The Hamburg Centre for Ultrafast Imaging, Luruper Chaussee 149, 22761 Hamburg, Germany; Department of Chemistry, Institute for Biochemistry and Molecular Biology, University of Hamburg, Martin-Luther-King-Platz 6, 20146 Hamburg, Germany.
The Hamburg Centre for Ultrafast Imaging, Luruper Chaussee 149, 22761 Hamburg, Germany; Institute for Nanostructure and Solid State Physics, Department of Physics and Center for Free-Electron Laser Science, University of Hamburg, Luruper Chaussee 149, 22761 Hamburg, Germany.
Structure. 2020 Mar 3;28(3):348-354.e3. doi: 10.1016/j.str.2019.12.001. Epub 2019 Dec 30.
Recent structures of full-length ATP-binding cassette (ABC) transporter MsbA in different states indicate large conformational changes during the reaction cycle that involve transient dimerization of its nucleotide-binding domains (NBDs). However, a detailed molecular understanding of the structural changes and associated kinetics of MsbA upon ATP binding and hydrolysis is still missing. Here, we employed time-resolved small-angle X-ray scattering, initiated by stopped-flow mixing, to investigate the kinetics and accompanying structural changes of NBD dimerization (upon ATP binding) and subsequent dissociation (upon ATP hydrolysis) in the context of isolated NBDs as well as full-length MsbA in lipid nanodiscs. Our data allowed us to structurally characterize the major states involved in the process and determine time constants for NBD dimerization and dissociation. In the full-length protein, these structural transitions occur on much faster time scales, indicating close-proximity effects and structural coupling of the transmembrane domains with the NBDs.
最近全长度 ATP 结合盒(ABC)转运蛋白 MsbA 的结构表明,在反应循环中会发生较大的构象变化,涉及核苷酸结合域(NBD)的瞬时二聚化。然而,对于 MsbA 在 ATP 结合和水解时的结构变化及其相关动力学,仍然缺乏详细的分子理解。在这里,我们采用时间分辨小角 X 射线散射,通过停流混合启动,研究了在分离的 NBD 以及脂质纳米盘中全长 MsbA 中,NBD 二聚化(在 ATP 结合时)和随后的解离(在 ATP 水解时)的动力学及其伴随的结构变化。我们的数据使我们能够对该过程中涉及的主要状态进行结构表征,并确定 NBD 二聚化和解离的时间常数。在全长蛋白中,这些结构转变发生的速度要快得多,这表明跨膜结构域与 NBD 之间的近距离效应和结构耦合。