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从头设计类药性肽的最新进展。

Recent Advances Toward the Discovery of Drug-Like Peptides De novo.

机构信息

Isogenica Ltd. Little Chesterford, UK.

Paratopix Ltd. Bishop's Stortford, UK.

出版信息

Front Chem. 2015 Dec 18;3:69. doi: 10.3389/fchem.2015.00069. eCollection 2015.

Abstract

Peptides are important natural molecules that possess functions as diverse as antibiotics, toxins, venoms and hormones, for example. However, whilst these peptides have useful properties, there are many targets and pathways that are not addressed through the activities of natural peptidic compounds. In these circumstances, directed evolution techniques, such as phage display, have been developed to sample the diverse chemical and structural repertoire of small peptides for useful means. In this review, we consider recent concepts that relate peptide structure to drug-like attributes and how these are incorporated within display technologies to deliver peptides de novo with valuable pharmaceutical properties.

摘要

肽是重要的天然分子,具有多种功能,如抗生素、毒素、毒液和激素等。然而,尽管这些肽具有有用的特性,但仍有许多靶点和途径无法通过天然肽化合物的活性来解决。在这种情况下,已经开发了定向进化技术,如噬菌体展示,以从各种化学和结构的小肽库中筛选有用的方法。在这篇综述中,我们考虑了与肽结构相关的药物样属性的最新概念,以及如何将这些概念纳入展示技术中,以从头开始提供具有有价值的药物特性的肽。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9ea/4683170/e9567b62760b/fchem-03-00069-g0001.jpg

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