Jules Stein Eye Institute and Department of Chemistry and Biochemistry, University of California, Los Angeles, CA 90095, United States.
Curr Opin Struct Biol. 2013 Oct;23(5):725-33. doi: 10.1016/j.sbi.2013.06.008. Epub 2013 Jul 11.
Molecular flexibility over a wide time range is of central importance to the function of many proteins, both soluble and membrane. Revealing the modes of flexibility, their amplitudes, and time scales under physiological conditions is the challenge for spectroscopic methods, one of which is site-directed spin labeling EPR (SDSL-EPR). Here we provide an overview of some recent technological advances in SDSL-EPR related to investigation of structure, structural heterogeneity, and dynamics of proteins. These include new classes of spin labels, advances in measurement of long range distances and distance distributions, methods for identifying backbone and conformational fluctuations, and new strategies for determining the kinetics of protein motion.
分子在很宽的时间范围内的柔韧性对于许多蛋白质的功能至关重要,无论是可溶性蛋白质还是膜蛋白。揭示生理条件下的柔韧性模式、幅度和时间尺度是光谱方法面临的挑战,其中一种方法是定点自旋标记电子顺磁共振(SDSL-EPR)。本文提供了 SDSL-EPR 相关的一些最新技术进展的概述,这些进展涉及蛋白质结构、结构异质性和动力学的研究。其中包括新型自旋标记物、长程距离和距离分布测量技术的进步、用于识别骨架和构象波动的方法,以及用于确定蛋白质运动动力学的新策略。