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影响离子通道功能的蝎毒液成分。

Scorpion venom components that affect ion-channels function.

机构信息

Department of Molecular Medicine and Bioprocesses, Instituto de Biotecnologia, Universidad Nacional Autonoma de Mexico (UNAM), Avenida Universidad 2001, Colonia Chamilpa, Apartado Postal 510-3, Cuernavaca 62210, Morelos, Mexico.

出版信息

Toxicon. 2013 Dec 15;76:328-42. doi: 10.1016/j.toxicon.2013.07.012. Epub 2013 Jul 26.

Abstract

The number and types of venom components that affect ion-channel function are reviewed. These are the most important venom components responsible for human intoxication, deserving medical attention, often requiring the use of specific anti-venoms. Special emphasis is given to peptides that recognize Na(+)-, K(+)- and Ca(++)-channels of excitable cells. Knowledge generated by direct isolation of peptides from venom and components deduced from cloned genes, whose amino acid sequences are deposited into databanks are nowadays in the order of 1.5 thousands, out of an estimate biodiversity closed to 300,000. Here the diversity of components is briefly reviewed with mention to specific references. Structural characteristic are discussed with examples taken from published work. The principal mechanisms of action of the three different types of peptides are also reviewed. Na(+)-channel specific venom components usually are modifier of the open and closing kinetic mechanisms of the ion-channels, whereas peptides affecting K(+)-channels are normally pore blocking agents. The Ryanodine Ca(++)-channel specific peptides are known for causing sub-conducting stages of the channels conductance and some were shown to be able to internalize penetrating inside the muscle cells.

摘要

本文综述了影响离子通道功能的毒液成分的数量和类型。这些是最重要的毒液成分,可导致人类中毒,值得医学关注,通常需要使用特定的抗毒液。特别强调识别兴奋细胞的 Na(+)-、K(+)-和 Ca(++)-通道的肽。直接从毒液中分离肽和从克隆基因推导的成分的知识,其氨基酸序列被存入数据库,如今已达到 1500 种左右,而估计的生物多样性接近 30 万种。本文简要综述了成分的多样性,并提到了具体的参考文献。本文还以发表的工作为例讨论了结构特征。三种不同类型的肽的主要作用机制也进行了综述。Na(+)-通道特异性毒液成分通常是离子通道开放和关闭动力学机制的调节剂,而影响 K(+)-通道的肽通常是孔阻塞剂。Ryanodine Ca(++)-通道特异性肽已知可引起通道电导的亚传导阶段,一些肽被证明能够穿透进入肌肉细胞。

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5
Scorpion toxins specific for potassium (K+) channels: a historical overview of peptide bioengineering.
Toxins (Basel). 2012 Nov 1;4(11):1082-119. doi: 10.3390/toxins4111082.
8
Novel potassium channel blocker venom peptides from Mesobuthus gibbosus (Scorpiones: Buthidae).
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9
Binding modes and functional surface of anti-mammalian scorpion α-toxins to sodium channels.
Biochemistry. 2012 Oct 2;51(39):7775-82. doi: 10.1021/bi300776g. Epub 2012 Sep 21.

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