Towards Decoding the Sequence-Based Grammar Governing the Functions of Intrinsically Disordered Protein Regions

A substantial portion of the proteome consists of intrinsically disordered regions (IDRs) that do not fold into well-defined 3D structures yet perform numerous biological functions and are associated with a broad range of diseases. It has been a long-standing enigma how different IDRs successfully execute their specific functions. Further putting a spotlight on IDRs are recent discoveries of functionally relevant biomolecular assemblies, which in some cases form through liquid-liquid phase separation. At the molecular level, the formation of biomolecular assemblies is largely driven by weak, multivalent, but selective IDR-IDR interactions. Emerging experimental and computational studies suggest that the primary amino acid sequences of IDRs encode a variety of their interaction behaviors. In this review, we focus on findings and insights that connect sequence-derived features of IDRs to their conformations, propensities to form biomolecular assemblies, selectivity of interaction partners, functions in the context of physiology and disease, and regulation of function. We also discuss directions of future research to facilitate establishing a comprehensive sequence-function paradigm that will eventually allow prediction of selective interactions and specificity of function mediated by IDRs. (C) 2020 Elsevier Ltd. All rights reserved.

Automated summary

The proteome contains a significant portion of intrinsically disordered regions (IDRs) that perform various biological functions and are linked to different diseases despite lacking well-defined 3D structures. Recent discoveries of functionally relevant biomolecular assemblies, some forming through liquid-liquid phase separation, have brought attention to IDRs. Weak, multivalent, but selective interactions between IDRs primarily drive the formation of these biomolecular assemblies according to emerging experimental and computational studies.