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模糊的药物靶点:药物研发领域中的无序蛋白质

Fuzzy Drug Targets: Disordered Proteins in the Drug-Discovery Realm.

作者信息

Saurabh Suman, Nadendla Karthik, Purohit Shubh Sanket, Sivakumar Ponnurengam Malliappan, Cetinel Sibel

机构信息

Molecular Sciences Research Hub, Department of Chemistry, Imperial College London, London W12 0BZ, U.K.

Center for Misfolding Diseases, Yusuf Hamied Department of Chemistry, Lensfield Road, University of Cambridge, Cambridge CB2 1EW, U.K.

出版信息

ACS Omega. 2023 Mar 8;8(11):9729-9747. doi: 10.1021/acsomega.2c07708. eCollection 2023 Mar 21.

Abstract

Intrinsically disordered proteins (IDPs) and regions (IDRs) form a large part of the eukaryotic proteome. Contrary to the structure-function paradigm, the disordered proteins perform a myriad of functions . Consequently, they are involved in various disease pathways and are plausible drug targets. Unlike folded proteins, that have a defined structure and well carved out drug-binding pockets that can guide lead molecule selection, the disordered proteins require alternative drug-development methodologies that are based on an acceptable picture of their conformational ensemble. In this review, we discuss various experimental and computational techniques that contribute toward understanding IDP "structure" and describe representative pursuances toward IDP-targeting drug development. We also discuss ideas on developing rational drug design protocols targeting IDPs.

摘要

内在无序蛋白质(IDP)和内在无序区域(IDR)构成了真核生物蛋白质组的很大一部分。与结构-功能范式相反,无序蛋白质执行着无数种功能。因此,它们参与各种疾病途径,并且是合理的药物靶点。与具有确定结构和精心设计的可指导先导分子选择的药物结合口袋的折叠蛋白不同,无序蛋白质需要基于其构象集合的可接受图景的替代药物开发方法。在本综述中,我们讨论了有助于理解IDP“结构”的各种实验和计算技术,并描述了针对IDP靶向药物开发的代表性研究。我们还讨论了开发针对IDP的合理药物设计方案的想法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e842/10034788/a99b2bb3d1ea/ao2c07708_0001.jpg

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