Qu Y, Liang S, Ding J, Ma L, Zhang R, Gu X
National Laboratory of Protein Engineering and Plant Engineering, Peking University, Beijing, China.
J Protein Chem. 1995 Oct;14(7):549-57. doi: 10.1007/BF01886881.
The complete sequence-specific assignments of resonances in the 1H-NMR spectrum of huwentoxin-I from the Chinese bird spider, Selencocosmia huwena, is described. A combination of two-dimensional NMR experiments including 2D-COSY, 2D-NOESY, and 2D-TOCSY has been employed on samples of the toxin dissolved in D2O and in H2O for assignment purposes. Protons belonging to spin systems for each of the 33 amino acids were identified. The sequence-specific assignments were facilitated by the identification of d alpha N connectivities on the fingerprint regions of the COSY and NOESY spectra and were supported by the identification of dNN and d alpha N connectivities in the TOCSY and NOESY spectra. These studies provide a basis for the determination of the solution-phase conformation of this toxin.
本文描述了来自中国鸟蛛(虎纹捕鸟蛛,Selencocosmia huwena)的虎纹毒素-I(huwentoxin-I)的1H-NMR谱中共振峰的完整序列特异性归属。为了进行归属,对溶解于D2O和H2O中的毒素样品采用了二维NMR实验的组合,包括二维COSY、二维NOESY和二维TOCSY。确定了属于33个氨基酸中每个氨基酸自旋系统的质子。通过在COSY和NOESY谱的指纹区鉴定dαN连接性促进了序列特异性归属,并通过在TOCSY和NOESY谱中鉴定dNN和dαN连接性得到了支持。这些研究为确定该毒素的溶液相构象提供了基础。