4.8 Review

Intrinsically Disordered Proteins: Critical Components of the Wetware

Journal

CHEMICAL REVIEWS
Volume 122, Issue 6, Pages 6614-6633

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.chemrev.1c00848

Keywords

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Funding

  1. National Cancer Institute of the National Institutes of Health (Bethesda, MD) [P30CA033572]
  2. SERB (Science and Engineering Research Board), DST (Department of Science & Technology), and Government of India [SB/S2/RJN-049/2018]

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This article discusses the knowledge and unknown areas of intrinsically disordered proteins (IDPs), and explores the influence of IDPs on cell-fate decisions, as well as their potential roles in cellular phenotype switching, biological evolution, proteinaceous organelle formation, and transgenerational inheritance.
Despite the wealth of knowledge gained about intrinsically disordered proteins (IDPs) since their discovery, there are several aspects that remain unexplored and, hence, poorly understood. A living cell is a complex adaptive system that can be described as a wetware-a metaphor used to describe the cell as a computer comprising both hardware and software and attuned to logic gates-capable of making decisions. In this focused Review, we discuss how IDPs, as critical components of the wetware, influence cell-fate decisions by wiring protein interaction networks to keep them minimally frustrated. Because IDPs lie between order and chaos, we explore the possibility that they can be modeled as attractors. Further, we discuss how the conformational dynamics of IDPs manifests itself as conformational noise, which can potentially amplify transcriptional noise to stochastically switch cellular phenotypes. Finally, we explore the potential role of IDPs in prebiotic evolution, in forming proteinaceous membrane-less organelles, in the origin of multi-cellularity, and in protein conformation-based transgenerational inheritance of acquired characteristics. Together, these ideas provide a new conceptual framework to discern how IDPs may perform critical biological functions despite their lack of structure.

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