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Dynamic nuclear polarization methods in solids and solutions to explore membrane proteins and membrane systems

机译:固体中的动态核极化方法和探索膜蛋白和膜系统的溶液

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Membrane proteins regulate vital cellular processes, including signaling, ion transport, and vesicular trafficking. Obtaining experimental access to their structures, conformational fluctuations, orientations, locations, and hydration in membrane environments, as well as the lipid membrane properties, is critical to understanding their functions. Dynamic nuclear polarization (DNP) of frozen solids can dramatically boost the sensitivity of current solid-state nuclear magnetic resonance tools to enhance access to membrane protein structures in native membrane environments. Overhauser DNP in the solution state can map out the local and site-specific hydration dynamics landscape of membrane proteins and lipid membranes, critically complementing the structural and dynamics information obtained by electron paramagnetic resonance spectroscopy. Here, we provide an overview of how DNP methods in solids and solutions can significantly increase our understanding of membrane protein structures, dynamics, functions, and hydration in complex biological membrane environments.
机译:膜蛋白调节重要的细胞过程,包括信号传导,离子转运和囊泡运输。在膜环境中获得对它们的结构,构象波动,方向,位置和水合作用以及脂质膜特性的实验性访问对于了解其功能至关重要。冷冻固体的动态核极化(DNP)可以显着提高当前固态核磁共振工具的灵敏度,以增强对天然膜环境中膜蛋白结构的获取。溶液状态下的Overhauser DNP可以绘制出膜蛋白和脂质膜的局部和特定位置水合作用动力学图,从而对通过电子顺磁共振波谱获得的结构和动力学信息进行关键性补充。在这里,我们概述了固体和溶液中的DNP方法如何显着提高我们对复杂生物膜环境中膜蛋白结构,动力学,功能和水合的了解。

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