School of Physics and Astronomy, University of Leeds, Leeds, United Kingdom.
Weill Cornell Medicine, Department of Anesthesiology, New York, NY, United States.
Methods Enzymol. 2021;652:127-159. doi: 10.1016/bs.mie.2021.03.011. Epub 2021 Apr 24.
Channels and transporters are vital for transmembrane transport of ions and solutes, and also of larger compounds such as lipids and macromolecules. Therefore, they are crucial in many biological processes such as sensing, signal transduction, and the regulation of the distribution of molecules. Dysfunctions of these membrane proteins are associated to numerous diseases, and their interaction with drugs is critical in medicine. Understanding the behavior of channels and transporters requires structural and dynamic information to decipher the molecular mechanisms underlying their function. High-Speed Atomic Force Microscopy (HS-AFM) now allows the study of single transmembrane channels and transporters in action under physiological conditions, i.e., at ambient temperature and pressure, in physiological buffer and in a membrane, and in a most direct, label-free manner. In this chapter, we discuss the HS-AFM sample preparation, application, and data analysis protocols to study the structural and conformational dynamics of membrane-embedded channels and transporters.
通道和转运蛋白对于离子和溶质的跨膜运输至关重要,对于脂质和大分子等较大化合物的运输也是如此。因此,它们在许多生物过程中至关重要,如感应、信号转导和分子分布的调节。这些膜蛋白的功能障碍与许多疾病有关,它们与药物的相互作用在医学中至关重要。了解通道和转运蛋白的行为需要结构和动态信息,以破译它们功能的分子机制。高速原子力显微镜(HS-AFM)现在允许在生理条件下研究单个跨膜通道和转运蛋白的作用,即在环境温度和压力下、在生理缓冲液中和在膜中,并以最直接、无标记的方式进行。在本章中,我们讨论了 HS-AFM 的样品制备、应用和数据分析方案,以研究膜嵌入通道和转运蛋白的结构和构象动力学。