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Pseudo-4D triple resonance experiments to resolve HN overlap in the backbone assignment of unfolded proteins

机译:伪4D三重共振实验可解决未折叠蛋白骨架分配中的HN重叠

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摘要

The solution NMR resonance assignment of the protein backbone is most commonly carried out using triple resonance experiments that involve 15N and 1HN resonances. The assignment becomes problematic when there is resonance overlap of 15N-1HN cross peaks. For such residues, one cannot unambiguously link the "left" side of the NH root to the "right" side, and the residues associated with such overlapping HN resonances remain often unassigned. Here we present a solution to this problem: a hybrid (4d,3d) reduced-dimensionality HN(CO)CA(CON)CA sequence. In this experiment, the Ca(i) resonance is modulated with the frequency of the Ca(i-1) resonance, which helps in resolving the ambiguity involved in connecting the Ca(i) and Ca(i-1) resonances for overlapping NH roots. The experiment has limited sensitivity, and is only suited for small or unfolded proteins. In a companion experiment, (4d,3d) reduced-dimensionality HNCO(N)CA, the Ca(i) resonance is modulated with the frequency of the CO(i-1) resonance, hence resolving the ambiguity existent in pairing up the Ca(i) and CO(i-1) resonances for overlapping NH roots.
机译:蛋白质骨架的溶液NMR共振分配最常见的是使用涉及15N和1HN共振的三重共振实验进行。当15N-1HN交叉峰的共振重叠时,分配就变得有问题。对于此类残基,不能将NH根的“左侧”明确链接到“右侧”,并且与此类重叠的HN共振相关的残基经常保持未分配状态。在这里,我们提出一个解决此问题的方法:混合(4d,3d)降维HN(CO)CA(CON)CA序列。在此实验中,Ca(i)共振是通过Ca(i-1)共振的频率进行调制的,这有助于解决连接NH重叠的Ca(i)和Ca(i-1)共振所涉及的歧义。根。该实验灵敏度有限,仅适用于小的或未折叠的蛋白质。在一个伴随实验中,(4d,3d)降维HNCO(N)CA,Ca(i)共振被CO(i-1)共振的频率调制,因此解决了配对Ca时存在的歧义。 (i)和CO(i-1)重叠的NH根共振。

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