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1H-NMR 共振的序列特异性归属及京蝎毒素-I二级结构的确定

Sequence-specific assignment of 1H-NMR resonance and determination of the secondary structure of Jingzhaotoxin-I.

作者信息

Zeng Xiong-Zhi, Zhu Qi, Liang Song-Ping

机构信息

College of Life Sciences, Hunan Normal University, Changsha 410081, China.

出版信息

Acta Biochim Biophys Sin (Shanghai). 2005 Aug;37(8):567-72. doi: 10.1111/j.1745-7270.2005.00078.x.

Abstract

Jingzhaotoxin-I (JZTX-I) purified from the venom of the spider Chilobrachys jingzhao is a novel neurotoxin preferentially inhibiting cardiac sodium channel inactivation by binding to receptor site 3. The structure of this toxin in aqueous solution was investigated using 2-D 1H-NMR techniques. The complete sequence-specific assignments of proton resonance in the 1H-NMR spectra of JZTX-I were obtained by analyzing a series of 2-D spectra, including DQF-COSY, TOCSY and NOESY spectra, in H2O and D2O. All the backbone protons except for Gln4 and more than 95% of the side-chain protons were identified by d alphaN, d alphadelta, d betaN and d NN connectivities in the NOESY spectrum. These studies provide a basis for the further determination of the solution conformation of JZTX-I. Furthermore, the secondary structure of JZTX-I was identified from NMR data. It consists mainly of a short triple-stranded antiparallel beta-sheet with Trp7-Cys9, Phe20-Lys23 and Leu28-Trp31. The characteristics of the secondary structure of JZTX-I are similar to those of huwentoxin-I (HWTX-I) and hainantoxin-IV (HNTX-IV), whose structures in solution have previously been reported.

摘要

从蜘蛛敬钊缨毛蛛毒液中纯化得到的敬钊毒素-I(JZTX-I)是一种新型神经毒素,它通过与受体位点3结合优先抑制心脏钠通道失活。利用二维¹H-NMR技术研究了该毒素在水溶液中的结构。通过分析一系列二维谱,包括在H₂O和D₂O中的双量子滤波相关谱(DQF-COSY)、全相关谱(TOCSY)和核Overhauser效应谱(NOESY),获得了JZTX-I的¹H-NMR谱中质子共振的完整序列特异性归属。通过NOESY谱中的dαN、dαδ、dβN和dNN连接关系鉴定出除Gln4外的所有主链质子以及超过95%的侧链质子。这些研究为进一步确定JZTX-I的溶液构象提供了基础。此外,从NMR数据中鉴定出JZTX-I的二级结构。它主要由一个短的三股反平行β-折叠组成,包含Trp7-Cys9、Phe20-Lys23和Leu28-Trp31。JZTX-I二级结构的特征与虎纹毒素-I(HWTX-I)和海南毒素-IV(HNTX-IV)相似,它们在溶液中的结构此前已有报道。

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