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AA肽的合成。

Synthesis of AApeptides.

作者信息

Niu Youhong, Hu Yaogang, Wu Haifan, Cai Jianfeng

机构信息

Department of Chemistry, University of South Florida, Tampa, FL, USA.

出版信息

Methods Mol Biol. 2013;1081:35-46. doi: 10.1007/978-1-62703-652-8_3.

Abstract

The creation and development of nonnatural peptidomimetics has become an area of increasing significance in bioorganic and chemical biology. A wide range of new peptide mimics with novel structures and functions are urgently needed to be explored in order to identify potential drug candidates and targeted probes, and to study protein functions. AApeptides are a new class of peptide mimics based on chiral PNA backbone. They are resistant to proteolytic degradation and have limitless potential for diversification. They have been found to have a wide variety of biological applications including cellular translocation, disruption of protein-protein interactions, formation of nanostructures, antimicrobial activity, etc. The synthesis of AApeptides is modular and straightforward. In this chapter, methods for the synthesis of AApeptides (including different subclasses) are described.

摘要

非天然肽模拟物的创制与发展已成为生物有机化学和化学生物学中一个日益重要的领域。为了鉴定潜在的候选药物和靶向探针,并研究蛋白质功能,迫切需要探索一系列具有新颖结构和功能的新型肽模拟物。AA肽是一类基于手性肽核酸骨架的新型肽模拟物。它们抗蛋白水解降解,具有无限的多样化潜力。已发现它们具有广泛的生物学应用,包括细胞转运、破坏蛋白质-蛋白质相互作用、形成纳米结构、抗菌活性等。AA肽的合成是模块化且直接的。在本章中,将描述AA肽(包括不同亚类)的合成方法。

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