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大环肽配体发展的前路。

The Road Ahead for the Development of Macrocyclic Peptide Ligands.

机构信息

Sydney Analytical, School of Life and Environmental Sciences and School of Chemistry , The University of Sydney , Sydney , NSW 2006 , Australia.

出版信息

Biochemistry. 2020 Jan 21;59(2):139-145. doi: 10.1021/acs.biochem.9b00802. Epub 2019 Oct 16.

Abstract

Macrocyclic peptides make up an emerging class of candidate therapeutics and chemical probes, with properties that make them potentially applicable to a wide range of targets that are intractable using current pharmacological agents. Additionally, a number of biochemical screening strategies have been developed, particularly over the past decade, that allow for the massively parallel screening of cyclic peptide libraries of up to 1 trillion compounds or more, leading to the isolation of molecules with exceptional target affinity, selectivity, and bioactivity. Clinical development of compounds derived from such screens is already underway, but the nature of these molecules means that such development is likely to follow pathways different from those of traditional small molecule drugs or well-established biologics such as monoclonal antibodies. In addition, recent work has shown that the biochemical techniques used to identify macrocyclic peptides can also be used to rapidly characterize and optimize them. These findings are likely to facilitate the development of these compounds as chemical probes and as therapeutics for areas of unmet medical need.

摘要

大环肽是一类新兴的候选治疗药物和化学探针,具有使其能够潜在应用于广泛的靶点的特性,而这些靶点使用当前的药理学制剂是难以处理的。此外,已经开发了许多生化筛选策略,特别是在过去十年中,这些策略允许对多达 1 万亿种化合物或更多化合物的环状肽文库进行大规模平行筛选,从而分离出具有优异靶标亲和力、选择性和生物活性的分子。源自此类筛选的化合物的临床开发已经在进行中,但这些分子的性质意味着此类开发可能遵循与传统小分子药物或单克隆抗体等成熟生物制剂不同的途径。此外,最近的工作表明,用于鉴定大环肽的生化技术也可用于快速表征和优化它们。这些发现可能有助于这些化合物作为化学探针以及作为治疗未满足医疗需求领域的治疗药物的发展。

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