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A High Resolution Solid State NMR Approach for the Structural Studies of Bicelles

机译:一种高分辨率的核磁共振结构的Bicelles结构研究。

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摘要

Bicelles are increasingly being used as membrane mimicking systems in NMR experiments to investigate the structure of membrane proteins. In this study, we demonstrate the effectiveness of a 2D solid-state NMR approach that can be used to measure the structural constraints such as heteronuclear dipolar couplings between 1H, 13C and 31P nuclei in bicelles without the need for isotopic enrichment. This method does not require a high radio frequency power unlike the presently used rotating-frame separated-local-field (SLF) techniques like PISEMA. In addition, multiple dipolar couplings can be measured accurately and the presence of a strong dipolar coupling does not suppress the weak couplings. High resolution spectra obtained from magnetically aligned DMPC:DHPC bicelles even in the presence of peptides suggest that this approach will be useful in understanding lipid-protein interactions that play a vital role in shaping up the function of membrane proteins.
机译:在NMR实验中,越来越多的Bicelles被用作膜模拟系统,以研究膜蛋白的结构。在这项研究中,我们证明了二维固态NMR方法的有效性,该方法可用于测量结构约束,例如 1 H, 13 C之间的异核偶极偶合和 31 P细胞核中不需要同位素富集。与目前使用的旋转帧分离局部场(SLF)技术(如PISEMA)不同,此方法不需要高射频功率。另外,可以精确地测量多个偶极耦合,并且强偶极耦合的存在不会抑制弱耦合。即使在存在肽的情况下,从磁性排列的DMPC:DHPC Bicells获得的高分辨率光谱也表明,这种方法将有助于理解脂蛋白相互作用,而脂蛋白相互作用在塑造膜蛋白的功能中起着至关重要的作用。

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