NMR-Based Methods for Protein Analysis

Yunfei Hu(Chinese Academy of Sciences), Kai Cheng(Chinese Academy of Sciences), Lichun He(Chinese Academy of Sciences), Xu Zhang(Chinese Academy of Sciences), Bin Jiang(Chinese Academy of Sciences), Ling Jiang(Chinese Academy of Sciences), Conggang Li(Chinese Academy of Sciences), Guan Wang(Chinese Academy of Sciences), Yunhuang Yang(Chinese Academy of Sciences), Maili Liu(Chinese Academy of Sciences)
Analytical Chemistry
January 13, 2021
Cited by 189

Abstract

Nuclear magnetic resonance (NMR) spectroscopy is a well-established method for analyzing protein structure, interaction, and dynamics at atomic resolution and in various sample states including solution state, solid state, and membranous environment. Thanks to rapid NMR methodology development, the past decade has witnessed a growing number of protein NMR studies in complex systems ranging from membrane mimetics to living cells, which pushes the research frontier further toward physiological environments and offers unique insights in elucidating protein functional mechanisms. In particular, in-cell NMR has become a method of choice for bridging the huge gap between structural biology and cell biology. Herein, we review the recent developments and applications of NMR methods for protein analysis in close-to-physiological environments, with special emphasis on in-cell protein structural determination and the analysis of protein dynamics, both difficult to be accessed by traditional methods.


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