[固相肽合成:对动物毒液分子物质增值的兴趣]。

S Aidi-Knani, H Ghodhbane, Ch Mourre, J Benhamida, S Jean-Marc, I Regaya
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引用次数: 0

摘要

来自动物毒液的毒素是小肽分子,能够与广泛的特定细胞靶标相互作用,以调节其活性,这使它们能够在许多生理和病理过程中发挥作用。最近,结构和药理学研究表明,这些生物制剂参与许多疾病的发病机制,如糖尿病、癌症瘫痪、自身免疫性疾病或神经系统疾病。尽管如此,从蝎子毒液中提取的这些肽仍然不能提供足够的数量来进行药理学和结构功能研究。固相肽合成(SPPS)是一种方法,允许我们从这些肽毒素中生产无限制数量的结构类似物。在本文中;我们将尝试强调这种方法的重要性,以及肽工程在一般情况下,在获得感兴趣的肽。我们还将阐明在化学合成过程中遇到的一些问题,并说明如何克服这些问题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Solid phase peptide synthesis: interest in the valorization of molecular substances from animal venoms].

Toxins from animal venoms are small peptide molecules able to interact with a wide range of specific cellular targets in order to modulate their activity, which enables them to act in many physiological and pathological processes. Recently, structuralandpharmacologicalstudieshaveshown the involvement of these biological agents in the pathogenesis of many diseases like diabetes, cancer paralysis, autoimmune diseases or neurological disorders. Nevertheless, the only punfication from scorpion venoms of theses peptides still doesn't offer sufficient quantities to allow conducting the pharmacological and structure-function studies. The solid phases peptide synthesis (SPPS) is a methodology that allows us to produce non-limited quantities of structural analogsfrom these peptides-toxins in. In this paper; we will try to highlight the importance of this methodology, and peptide engineering in general, in obtaining peptides of interest. We are also going to elucidate the problems encountered during the chemical synthesis of some betides and explain how to overcome them.

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