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不含二硫键的蝎毒肽:综述

Scorpion venom peptides with no disulfide bridges: a review.

作者信息

Almaaytah Ammar, Albalas Qosay

机构信息

Department of Pharmaceutical Technology, Faculty of Pharmacy, Jordan University of Science and Technology, Irbid, Jordan.

Department of Medicinal Chemistry and Pharmacognosy, Faculty of Pharmacy, Jordan University of Science and Technology, Irbid, Jordan.

出版信息

Peptides. 2014 Jan;51:35-45. doi: 10.1016/j.peptides.2013.10.021. Epub 2013 Oct 31.

Abstract

Scorpion venoms are rich sources of biologically active peptides that are classified into disulfide-bridged peptides (DBPs) and non-disulfide-bridged peptides (NDBPs). DBPs are the main scorpion venom components responsible for the neurotoxic effects observed during scorpion envenomation as they usually target membrane bound ion channels of excitable and non-excitable cells. Several hundred DBPs have been identified and functionally characterized in the past two decades. The NDBPs represent a novel group of molecules that have gained great interest only recently due to their high diversity both in their primary structures and bioactivities. This review provides an overview of scorpion NDBPs focusing on their therapeutic applications, modes of discovery, mechanisms of NDBPs genetic diversity and structural properties. It also provides a simple classification for NDBPs that could be adopted and applied to other NDBPs identified in future studies.

摘要

蝎毒是生物活性肽的丰富来源,这些生物活性肽可分为二硫键连接的肽(DBP)和非二硫键连接的肽(NDBP)。DBP是蝎毒的主要成分,在蝎蜇伤时会产生神经毒性作用,因为它们通常靶向可兴奋细胞和非可兴奋细胞膜结合的离子通道。在过去二十年中,已鉴定出数百种DBP并对其进行了功能表征。NDBP代表了一类新型分子,由于其一级结构和生物活性的高度多样性,直到最近才引起了极大的关注。本综述概述了蝎NDBP,重点介绍了它们的治疗应用、发现模式、NDBP遗传多样性机制和结构特性。它还为NDBP提供了一种简单的分类方法,可用于未来研究中鉴定出的其他NDBP。

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