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设计和优化新型抗菌肽:并非所有靶标都一样。

Designing and optimizing new antimicrobial peptides: all targets are not the same.

机构信息

Fundación Instituto de Inmunología de Colombia - FIDIC, Receptor-Ligand Department , Bogotá D.C , Colombia.

Universidad del Rosario, School of Medicine and Health Sciences , Bogotá D.C. , Colombia.

出版信息

Crit Rev Clin Lab Sci. 2019 Sep;56(6):351-373. doi: 10.1080/10408363.2019.1631249. Epub 2019 Aug 9.

Abstract

Because the resistance of microorganisms to the available antibiotics is a growing healthcare problem worldwide, the search for new antimicrobial peptides (AMPs) that provide useful therapeutic options has been increasing in importance. Many initial candidates have had to be discarded after having advanced to the preclinical and clinical stages. This has led to substantial losses in terms of time and money. For that reason, the essential characteristics of AMPs (i.e. their activity, selectivity, stability in physiological conditions and low production cost) must be considered in their design. In addition, peptides could be active against several kinds of cells with activity and selectivity resulting from interaction with multiple target cell components, which sometimes are present in mammalian cells as well. Thus, the cellular composition is important in the AMP-target cell interaction and must be considered in the design of AMPs, too. This review describes general aspects of AMP design, limitations concerning their therapeutic application, and optimization strategies for overcoming such limitations.

摘要

由于微生物对现有抗生素的耐药性是全球范围内日益严重的医疗保健问题,因此,寻找新的抗菌肽 (AMPs) 以提供有用的治疗选择变得越来越重要。许多最初的候选药物在进入临床前和临床阶段后不得不被淘汰。这在时间和金钱方面造成了巨大的损失。因此,在设计 AMP 时必须考虑其基本特性(即活性、选择性、生理条件下的稳定性和低成本生产)。此外,肽可以针对多种细胞发挥作用,其活性和选择性源于与多个靶细胞成分的相互作用,而这些成分有时也存在于哺乳动物细胞中。因此,细胞组成在 AMP-靶细胞相互作用中很重要,在 AMP 的设计中也必须考虑到这一点。本文综述了 AMP 设计的一般方面、其治疗应用的局限性以及克服这些局限性的优化策略。

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