Ambadipudi Susmitha, Zweckstetter Markus
a German Center for Neurodegenerative Diseases (DZNE) , 37077 Göttingen , Germany.
b Department for NMR-based Structural Biology , Max Planck Institute for Biophysical Chemistry , 37077 Göttingen , Germany.
Expert Opin Drug Discov. 2016;11(1):65-77. doi: 10.1517/17460441.2016.1107041. Epub 2015 Nov 7.
Intrinsically disordered proteins (IDPs) and intrinsically disordered protein regions (IDPRs) have gained wide recognition over the past decade due to their versatile roles in cell physiology and pathology. A large repertoire of IDPs/IDPRs has been implicated in numerous diseases, making them potential targets for therapeutic intervention. Recent advances in experimental methods and computational approaches have enabled detection and characterization of these highly dynamic proteins at atomistic detail, thus facilitating disorder/dynamic-based drug discovery.
This article presents an overview of the functional relevance and pathological implications of IDPs/IDPRs in cells. The authors outline the currently available experimental methods employed for structural characterization of these proteins. They also exemplify the practical limitations encountered during such characterization and ways to overcome them. Taken together, the article discusses the plausibility of exploiting protein disorder for drug targeting.
Disorder-based drug targeting is gearing up in the realm of novel drug discovery approaches. Tools for probing the molecular features of IDPs and IDPRs are rapidly improving and start to provide accurate descriptions of the complex ensembles populated by IDPs/IDPRs. They thus pave the way for the development of drug molecules, which specifically target disease-associated disorder.
在过去十年中,内在无序蛋白(IDP)和内在无序蛋白区域(IDPR)因其在细胞生理和病理过程中的多种作用而得到广泛认可。大量的IDP/IDPR与多种疾病有关,使其成为治疗干预的潜在靶点。实验方法和计算方法的最新进展使得能够在原子水平上详细检测和表征这些高度动态的蛋白质,从而促进基于无序/动态的药物发现。
本文概述了IDP/IDPR在细胞中的功能相关性和病理意义。作者概述了目前用于这些蛋白质结构表征的实验方法。他们还举例说明了在这种表征过程中遇到的实际限制以及克服这些限制的方法。总之,本文讨论了利用蛋白质无序进行药物靶向的可行性。
基于无序的药物靶向正在新型药物发现方法领域兴起。用于探测IDP和IDPR分子特征的工具正在迅速改进,并开始提供对IDP/IDPR所占据的复杂集合体的准确描述。因此,它们为开发专门针对疾病相关无序的药物分子铺平了道路。