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帝王蝎毒素K-α(PiTX-Kα)的溶液结构,一种A型钾通道的选择性阻滞剂。

Solution structure for Pandinus toxin K-alpha (PiTX-K alpha), a selective blocker of A-type potassium channels.

作者信息

Tenenholz T C, Rogowski R S, Collins J H, Blaustein M P, Weber D J

机构信息

Department of Biochemistry, University of Maryland School of Medicine, Baltimore 21201, USA.

出版信息

Biochemistry. 1997 Mar 11;36(10):2763-71. doi: 10.1021/bi9628432.

Abstract

PiTX-K alpha, a 35-residue peptide recently isolated from the venom of Pandinus imperator, blocks the rapidly inactivating (A-type) K+ channel(s) in rat brain synaptosomes and the cloned Kv 1.2 potassium channel at very low toxin concentrations (6 nM and 32 pM, respectively) [Rogowski, R. S., Collins, J. H., O'Neil, T. J., Gustafson, T. A., Werkman, T. A., Rogawski, M. A., Tenenholz, T. C., Weber, D. J., & Blaustein, M. P. (1996) Mol. Pharmacol. 50, 1167-1177]. The three-dimensional structure of PiTX-K alpha was determined using NMR spectroscopy in order to understand its selectivity and affinity toward K+ channels. PiTX-K alpha was found to have an alpha-helix from residues 10 to 21 and two beta-strands (betaI, 26-28; betaII, 33-35) connected by a type II beta-turn to form a small antiparallel beta-sheet. Three disulfide bonds, which are conserved in all members of the charybdotoxin family (alpha-K toxins), anchor one face of the alpha-helix to the beta-sheet. The N-terminal portion of PiTX-K alpha has three fewer residues than other alpha-K toxins such as charybdotoxin. Rather than forming a third beta-strand as found for other alpha-K toxins, the N-terminal region of PiTX-K alpha adopts an extended conformation. This structural difference in PiTX-K alpha together with differences in sequence at Pro-10, Tyr-14, and Asn-25 (versus Ser-10, Trp-14, and Arg-25 in CTX) may explain why PiTX-K alpha does not block maxi-K+ channels. Differences in three-dimensional structure between PiTX-K alpha and charybdotoxin are also observed in both the tight turn and the loop that connects the first beta-strand to the alpha-helix. As a result, side chains of two residues (Tyr-23 and Arg-31) are in regions of PiTX-K alpha that probably interact with rapidly inactivating A-type K+ channels. The analogous residues in charybdotoxin are positioned differently on the toxin surface. Thus, the locations of Tyr-23 and Arg-31 side chains in PiTX-K alpha could explain why this toxin blocks A-type channels at much lower concentrations than does charybdotoxin.

摘要

PiTX-Kα是一种最近从帝王蝎毒液中分离出的由35个氨基酸残基组成的肽,在极低的毒素浓度(分别为6 nM和32 pM)下就能阻断大鼠脑突触体中快速失活的(A型)钾通道以及克隆的Kv 1.2钾通道[罗戈夫斯基,R. S.,柯林斯,J. H.,奥尼尔,T. J.,古斯塔夫森,T. A.,韦克曼,T. A.,罗加夫斯基,M. A.,特嫩霍尔兹,T. C.,韦伯,D. J.,&布劳斯坦,M. P.(1996年)。分子药理学。50,1167 - 1177]。为了了解PiTX-Kα对钾通道的选择性和亲和力,利用核磁共振光谱法测定了其三维结构。发现PiTX-Kα从第10位到第21位残基有一个α螺旋,以及两条β链(βI,26 - 28;βII,33 - 35),通过一个II型β转角相连形成一个小的反平行β折叠。在所有的卡律布狄毒素家族成员(α-K毒素)中都保守的三个二硫键,将α螺旋的一个面锚定到β折叠上。PiTX-Kα的N端部分比其他α-K毒素如卡律布狄毒素少三个残基。PiTX-Kα的N端区域没有像其他α-K毒素那样形成第三条β链,而是采用了一种伸展的构象。PiTX-Kα的这种结构差异以及Pro-10、Tyr-14和Asn-25处(与CTX中的Ser-10、Trp-14和Arg-25相比)的序列差异,可能解释了为什么PiTX-Kα不阻断大电导钾通道。在紧密转角以及连接第一条β链和α螺旋的环中,也观察到了PiTX-Kα和卡律布狄毒素在三维结构上的差异。因此,两个残基(Tyr-23和Arg-31)的侧链位于PiTX-Kα中可能与快速失活的A型钾通道相互作用的区域。卡律布狄毒素中的类似残基在毒素表面的位置不同。因此,PiTX-Kα中Tyr-23和Arg-31侧链的位置可以解释为什么这种毒素阻断A型通道的浓度比卡律布狄毒素低得多。

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