克服基于肽的治疗方法的缺点

C. Lamers
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引用次数: 16

摘要

多肽由于其药代动力学行为(包括血浆稳定性、膜渗透性和循环半衰期)等不利特性,传统上被认为是不理想的候选药物。尽管如此,近年来,解决这些缺点的一般策略已经建立,并且肽由于其结合抗体和小分子优势的独特能力,随后作为药物获得越来越多的兴趣。大环肽是药物开发工作的一个特别焦点,因为它们能够解决所谓的“不可药物”目标,其特征是缺乏结合口袋的大而扁平的蛋白质表面。在这里,总结了迄今为止为适应临床使用的肽开发的主要策略,这可能很快有助于迎来一个由基于肽的治疗高度塑造的时代。尽管如此,在肽疗法被广泛接受之前,有限的膜渗透性仍有待克服。
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Overcoming the shortcomings of peptide-based therapeutics
Peptides have traditionally been perceived as poor drug candidates due to unfavorable characteristics mainly regarding their pharmacokinetic behavior, including plasma stability, membrane permeability and circulation half-life. Nonetheless, in recent years, general strategies to tackle those shortcomings have been established, and peptides are subsequently gaining increasing interest as drugs due to their unique ability to combine the advantages of antibodies and small molecules. Macrocyclic peptides are a special focus of drug development efforts due to their ability to address so called ‘undruggable’ targets characterized by large and flat protein surfaces lacking binding pockets. Here, the main strategies developed to date for adapting peptides for clinical use are summarized, which may soon help usher in an age highly shaped by peptide-based therapeutics. Nonetheless, limited membrane permeability is still to overcome before peptide therapeutics will be broadly accepted.
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