Genome Editing Research Center, Korea Research Institute of Bioscience and Biotechnology, Daejeon, 34141, Korea.
Mol Cells. 2018 Oct 31;41(10):889-899. doi: 10.14348/molcells.2018.0192. Epub 2018 Oct 10.
Intrinsically disordered proteins (IDPs) are highly unorthodox proteins that do not form three-dimensional structures under physiological conditions. The discovery of IDPs has destroyed the classical structure-function paradigm in protein science, 3-D structure = function, because IDPs even without well-folded 3-D structures are still capable of performing important biological functions and furthermore are associated with fatal diseases such as cancers, neurodegenerative diseases and viral pandemics. Pre-structured motifs (PreSMos) refer to transient local secondary structural elements present in the target-unbound state of IDPs. During the last two decades PreSMos have been steadily acknowledged as the critical determinants for target binding in dozens of IDPs. To date, the PreSMo concept provides the most convincing structural rationale explaining the IDP-target binding behavior at an atomic resolution. Here we present a brief developmental history of PreSMos and describe their common characteristics. We also provide a list of newly discovered PreSMos along with their functional relevance.
无规卷曲蛋白质(IDPs)是高度非常规的蛋白质,在生理条件下不会形成三维结构。IDPs 的发现打破了蛋白质科学中的经典结构-功能范式,即 3-D 结构=功能,因为 IDPs 即使没有良好折叠的 3-D 结构,仍然能够执行重要的生物学功能,并且与癌症、神经退行性疾病和病毒大流行等致命疾病有关。预结构基序(PreSMos)是指无规卷曲蛋白质在目标未结合状态下存在的瞬态局部二级结构元件。在过去的二十年中,PreSMos 已被逐步确认为数十种 IDPs 中靶标结合的关键决定因素。迄今为止,PreSMo 概念提供了最具说服力的结构原理,可在原子分辨率水平上解释 IDP-靶标结合行为。在这里,我们简要介绍了 PreSMos 的发展历史,并描述了它们的共同特征。我们还提供了一份新发现的 PreSMos 列表及其功能相关性。