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Perspective: next generation isotope-aided methods for protein NMR spectroscopy

机译:透视:下一代同位素 - 蛋白质NMR光谱的辅助方法

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In this perspective, we describe our efforts to innovate the current isotope-aided NMR methodology to investigate biologically important large proteins and protein complexes, for which only limited structural information could be obtained by conventional NMR approaches. At the present time, it is widely believed that only backbone amide and methyl signals are amenable for investigating such difficult targets. Therefore, our primary mission is to disseminate our novel knowledge within the biological NMR community; specifically, that any type of NMR signals other than methyl and amide groups can be obtained, even for quite large proteins, by optimizing the transverse relaxation properties by isotope labeling methods. The idea of "TROSY by isotope labeling" has been cultivated through our endeavors aiming to improve the original stereo-array isotope labeling (SAIL) method (Kainosho et al., Nature 440:52-57, 2006). The SAIL TROSY methods subsequently culminated in the successful observations of individual NMR signals for the side-chain aliphatic and aromatic (CH)-C-13 groups in large proteins, as exemplified by the 82 kDa single domain protein, malate synthase G. Meanwhile, the expected role of NMR spectroscopy in the emerging integrative structural biology has been rapidly shifting, from structure determination to the acquisition of biologically relevant structural dynamics, which are poorly accessible by X-ray crystallography or cryo-electron microscopy. Therefore, the newly accessible NMR probes, in addition to the methyl and amide signals, will open up a new horizon for investigating difficult protein targets, such as membrane proteins and supramolecular complexes, by NMR spectroscopy. We briefly introduce our latest results, showing that the protons attached to C-12-atoms give profoundly narrow H-1-NMR signals even for large proteins, by isolating them from the other protons using the selective deuteration. The direct H-1 observation methods exhibit the highest sen
机译:在这种观点中,我们描述了我们创新当前同位素辅助NMR方法的努力来研究生物学上重要的大蛋白质和蛋白质复合物,其仅通过常规NMR方法获得有限的结构信息。目前,众所周知,只有骨干酰胺和甲基信号均可用于研究这种困难的靶标。因此,我们的主要任务是在生物NMR社区中传播我们的小说知识;具体地,通过通过同位素标记方法优化横向松弛性能,即使对于相当大的蛋白,也可以获得除甲基和酰胺基团之外的任何类型的NMR信号。通过我们的努力来培养“由同位素标签”的思想,旨在改善原始立体声阵列同位素标签(帆)方法(Kainosho等,自然440:52-57,2006)。随后在大蛋白中的侧链脂族和芳族(CH)-C-13基团的单个NMR信号的成功观察中持续的帆疏水液方法,如82kDa单结构域蛋白,苹果酸合酶G.同时, NMR光谱在新出现的整合结构生物学中的预期作用一直在迅速转化,从结构测定从X射线晶体学或低温电子显微镜观察到的生物相关结构动力学。因此,除了甲基和酰胺信号之外,新近可接近的NMR探针将通过NMR光谱开辟用于研究难以调查膜蛋白和超分子复合物的难蛋白靶标的新视野。我们简要介绍了我们最新的结果,表明,即使使用选择性氘将它们与其他质子分离,也显示出C-12-原子的质子即使对于大型蛋白质,也可以使H-1-NMR信号较窄。直接H-1观察方法展示了最高的森

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