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抗菌肽的修饰与设计。

The Modification and Design of Antimicrobial Peptide.

机构信息

College of Animal Sciences, Jilin University, Changchun, Jilin Province, China.

The Center for Disease Control and Prevention in Jinan Military Area, No.36 East Wenhua Road, Jinan, Shandong Province, China.

出版信息

Curr Pharm Des. 2018;24(8):904-910. doi: 10.2174/1381612824666180213130318.

Abstract

The antimicrobial peptides (AMPs) are a group of unique naturally occurring anti-microbial compounds with around 50 amino acids. It represents promising therapeutic agents to the infectious disease without concerning about drug resistance. However, commercial development of these peptides for even the simplest application has been hindered by the limitations of sources, instability, toxicity and bioavailability. To improve the properties of the artificial synthesized AMPs, the modification and design are the hotspots of the AMPs research. In fact, more than half of the known AMPs are naturally modified. In this review, two types of modification strategies, biochemical modification and chemical modification were summarized. Although, the chemical modification is versatile and direct, the manufacturing cost is greatly increased compared to the antibiotics. With the recent progress of the protein modification enzyme, the biochemical modification of the antimicrobial peptide followed by heterologous expression has great application prospects.

摘要

抗菌肽(AMPs)是一组独特的天然抗菌化合物,大约由 50 个氨基酸组成。它是一种很有前途的治疗传染病的药物,而不用担心耐药性。然而,即使是最简单的应用,这些肽的商业开发也受到来源、不稳定性、毒性和生物利用度等方面的限制。为了改善人工合成 AMPs 的特性,修饰和设计是 AMPs 研究的热点。事实上,已知的 AMPs 中有一半以上是天然修饰的。在本综述中,总结了两种修饰策略,即生化修饰和化学修饰。虽然化学修饰具有通用性和直接性,但与抗生素相比,制造成本大大增加。随着蛋白质修饰酶的最新进展,抗菌肽的生化修饰后进行异源表达具有广阔的应用前景。

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