Department of Medical Biochemistry and Biophysics, Umeå University, S 901 87, Umeå, Sweden.
J Biomol NMR. 1999 Jun;14(2):169-74. doi: 10.1023/A:1008308307363.
We report a 3D constant-time HCANH experiment (CTSL-HCANH) that uses the slower relaxation of multiple-quantum coherence to increase sensitivity and provides high C(α) resolution. In this experiment the H(α) of the (H(α), C(α)) multiple quanta are selectively spin locked, so that H(α) chemical shift evolution and (1) H-(1)H J-dephasing become ineffective during the relatively long delay needed for C(α) to N coherence transfer. As compared to an HCANH experiment that uses C(α) single-quantum coherence, an average enhancement of 20% was observed on calmodulin in complex with the binding domain of the transcription factor SEF2-1. Compared to CBCANH the signal intensity is approximately twice as good. The favorable relaxation properties of multiple quanta, together with the outstanding C(α) resolution, make the experiment a very good complement to CBCANH and CBCA(CO)NH for sequential assignment of larger proteins for which deuteration is not yet necessary.
我们报告了一种 3D 等时 HCANH 实验(CTSL-HCANH),该实验利用多量子相干的较慢弛豫来提高灵敏度,并提供高 C(α)分辨率。在该实验中,(H(α), C(α))多重量子的 H(α)被选择性地自旋锁定,因此在 C(α)到 N 相干转移所需的相对较长的延迟期间,H(α)化学位移演化和(1)H-(1)H J 去相位变得无效。与使用 C(α)单量子相干的 HCANH 实验相比,在与转录因子 SEF2-1 的结合域结合的钙调蛋白上观察到平均增强 20%。与 CBCANH 相比,信号强度大约要好两倍。多量子的有利弛豫特性,加上出色的 C(α)分辨率,使得该实验成为 CBCANH 和 CBCA(CO)NH 的非常好的补充,用于对尚未需要氘化的更大蛋白质进行顺序分配。