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RNA结合大环肽

RNA-Binding Macrocyclic Peptides.

作者信息

Pal Sunit, 't Hart Peter

机构信息

Chemical Genomics Centre of the Max Planck Society, Max Planck Institute of Molecular Physiology, Dortmund, Germany.

出版信息

Front Mol Biosci. 2022 Apr 19;9:883060. doi: 10.3389/fmolb.2022.883060. eCollection 2022.

Abstract

Being able to effectively target RNA with potent ligands will open up a large number of potential therapeutic options. The knowledge on how to achieve this is ever expanding but an important question that remains open is what chemical matter is suitable to achieve this goal. The high flexibility of an RNA as well as its more limited chemical diversity and featureless binding sites can be difficult to target selectively but can be addressed by well-designed cyclic peptides. In this review we will provide an overview of reported cyclic peptide ligands for therapeutically relevant RNA targets and discuss the methods used to discover them. We will also provide critical insights into the properties required for potent and selective interaction and suggestions on how to assess these parameters. The use of cyclic peptides to target RNA is still in its infancy but the lessons learned from past examples can be adopted for the development of novel potent and selective ligands.

摘要

能够用强效配体有效地靶向RNA将开启大量潜在的治疗选择。关于如何实现这一点的知识在不断扩展,但一个悬而未决的重要问题是哪种化学物质适合实现这一目标。RNA的高度灵活性及其相对有限的化学多样性和无特征的结合位点可能难以进行选择性靶向,但精心设计的环肽可以解决这一问题。在这篇综述中,我们将概述已报道的针对与治疗相关的RNA靶点的环肽配体,并讨论用于发现它们的方法。我们还将对强效和选择性相互作用所需的特性提供关键见解,并就如何评估这些参数提出建议。使用环肽靶向RNA仍处于起步阶段,但从过去的例子中吸取的经验教训可用于开发新型强效和选择性配体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e7f9/9062085/78fc7027f8b2/fmolb-09-883060-g001.jpg

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