Department of Chemistry, College of Arts and Sciences, University of Alabama at Birmingham, CH266, 901 14th Street South, Birmingham, AL, 35294-1240, USA.
J Biomol NMR. 2020 Mar;74(2-3):119-124. doi: 10.1007/s10858-020-00305-1. Epub 2020 Feb 13.
Residual dipolar couplings (RDCs) provide valuable NMR parameters that can be used for structural calculation and verification. Measuring RDCs requires aligning macromolecules using one of various types of alignment media. Of different alignment media options, stretched or compressed polyacrylamide gels are advantageous due to their chemical stability. However, polyacrylamide interacts with proteins and significantly broadens NMR resonances. In this study, we found that the amide-containing compounds asparagine, glutamine and propionamide improve spectral quality of proteins in polyacrylamide gel without significantly reducing the magnitude of RDC values. Moreover, we showed that propionamide is an attractive additive that increases protein solubility without interfering with protein stability, ligand binding or NMR pulse width, suggesting its potential applications for our NMR methods.
残基偶极耦合(RDC)提供了有价值的 NMR 参数,可用于结构计算和验证。测量 RDC 需要使用各种类型的对齐介质对大分子进行对齐。在不同的对齐介质选项中,拉伸或压缩的聚丙烯酰胺凝胶由于其化学稳定性而具有优势。然而,聚丙烯酰胺会与蛋白质相互作用,显著拓宽 NMR 共振。在这项研究中,我们发现含酰胺的化合物天冬酰胺、谷氨酰胺和丙酰胺可改善聚丙烯酰胺凝胶中蛋白质的光谱质量,而不会显著降低 RDC 值的幅度。此外,我们表明丙酰胺是一种有吸引力的添加剂,它可以增加蛋白质的溶解度,而不会干扰蛋白质稳定性、配体结合或 NMR 脉冲宽度,这表明它在我们的 NMR 方法中有潜在的应用。