Sequence and chemical specificity define the functional landscape of intrinsically disordered regions

Intrinsically disordered regions (IDRs) pervasively engage in essential molecular functions, yet they are often poorly conserved as assessed by sequence alignment. To explore the seeming paradox of how sequence variability is compatible with persistent function, we examined the functional determinants for a poorly conserved but essential IDR. We show that IDR function depends on two distinct but related properties: sequence and chemical specificity. Whereas sequence specificity operates via binding motifs and depends on the precise order and identity of residues, chemical specificity reflects the sequence-encoded chemistry of multivalent interactions across an IDR and depends on local and global chemical properties. Unexpectedly, a binding motif essential in the wild-type IDR can be removed when compensatory changes to the sequence chemistry are introduced, highlighting the orthogonality and interoperability of these properties, and expanding the sequence space compatible with function. Our results provide a general framework for the functional constraints on IDR evolution.

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Publication Details

Journal
Nature Cell Biology
Published
2026-02-01
DOI
https://doi.org/10.1038/s41556-025-01867-8
Citations
1
Primary Topic
Protein Structure and Dynamics
Type
article
Field-Weighted Citation Impact
22.24
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article

Sequence and chemical specificity define the functional landscape of intrinsically disordered regions

Till Bartke, Franziska Kunert, Iris Langstein-Skora, Felix J. Metzner et al.
1 citations
Nature Cell Biology
Protein Structure and Dynamics
22.24
article

Sequence and chemical specificity define the functional landscape of intrinsically disordered regions

Till Bartke, Franziska Kunert, Iris Langstein-Skora, Felix J. Metzner, Wasim Aftab, Andrea Schmid, Drin Shabani, Ryan J. Emenecker, Hopfner Karl-Peter, Alex S. Holehouse, Maximilian J. Götz, Ulrich Gerland, Philipp Korber, Mary O.G. Richardson, Sarah Payer, Mariia Likhodeeva, Niccoló Pietrantoni, Frauke Huth, Lorenz Spechtenhauser, Sakthi K. Ravichandran, Valentina Valka
article en
1 citations

Abstract

Intrinsically disordered regions (IDRs) pervasively engage in essential molecular functions, yet they are often poorly conserved as assessed by sequence alignment. To explore the seeming paradox of how sequence variability is compatible with persistent function, we examined the functional determinants for a poorly conserved but essential IDR. We show that IDR function depends on two distinct but related properties: sequence and chemical specificity. Whereas sequence specificity operates via binding motifs and depends on the precise order and identity of residues, chemical specificity reflects the sequence-encoded chemistry of multivalent interactions across an IDR and depends on local and global chemical properties. Unexpectedly, a binding motif essential in the wild-type IDR can be removed when compensatory changes to the sequence chemistry are introduced, highlighting the orthogonality and interoperability of these properties, and expanding the sequence space compatible with function. Our results provide a general framework for the functional constraints on IDR evolution.

Nature Cell BiologyVol. 28(2)
Scuola Superiore Sant'Anna (IT), Washington University in St. Louis (US), Helmholtz Zentrum München (DE), LMU Klinikum (DE), Josep Carreras Leukaemia Research Institute (ES), Moderna Therapeutics (United States) (US), Max Planck Institute of Neurobiology (DE), Max Planck Institute of Biochemistry (DE), Living Systems (United States) (US), Technical University of Munich (DE), Ludwig-Maximilians-Universität München (DE)
Openalex Percentile: Top 1%
Protein Structure and Dynamics
22.24
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