Evidence map›Paper›PMID 41993527›Full record

ArticlebioRxiv : the preprint server for biology2026

Generative design of intrinsically disordered protein regions with IDiom.

Jason X Liu, Sebastian Ibarraran, Frank Hu, Abigail Park, Alexander R Dunn, Grant M Rotskoff

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In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Jason X LiuDepartment of Chemical Engineering, Stanford University, Stanford, CA 94305.
Sebastian IbarraranDepartment of Chemistry, Stanford University, Stanford, CA 94305.
Frank HuDepartment of Chemistry, Stanford University, Stanford, CA 94305.
Abigail ParkDepartment of Chemistry, Stanford University, Stanford, CA 94305.
Alexander R DunnDepartment of Chemical Engineering, Stanford University, Stanford, CA 94305.
Grant M RotskoffDepartment of Chemistry, Stanford University, Stanford, CA 94305.

Funding

Training in Myocardial Biology at Stanford (TIMBS)T32HL094274 · NHLBI · STANFORD UNIVERSITY · PI Euan A Ashley, Daniel Bernstein · 2010 to 2026
$5.0M
Molecular mechanisms underlying force transduction at cellular adhesion complexesR35GM130332 · NIGMS · STANFORD UNIVERSITY · PI Alexander R Dunn · 2019 to 2026
$4.9M
Generative multiscale models of biomolecular conformational dynamics: from fluctuations to many-component assembliesR35GM159834 · NIGMS · STANFORD UNIVERSITY · PI Grant Rotskoff · 2025 to 2026
$820k
NHLBI NIH HHS T32 HL094274NIGMS NIH HHS R35 GM130332NIGMS NIH HHS R35 GM159834
6 · The paper itself

Abstract

Intrinsically disordered protein regions are ubiquitous across all kingdoms of life. These structurally heterogeneous regions play central roles in cellular processes such as transcriptional regulation, cellular signaling, and subcellular organization, yet they have remained largely inaccessible to rational design. Structure-based generative methods are not applicable to proteins that lack a stable fold, and existing sequence-based approaches for disordered regions rely on sampling methods that do not capture the evolutionary statistics of natural disordered regions. Here, we introduce IDiom, an autoregressive protein language model trained on 37 million intrinsically disordered region sequences curated from the AlphaFold Database. Trained using a fill-in-the-middle data augmentation, IDiom generates disordered region sequences conditioned on their surrounding structured context, as well as fully disordered proteins without any context. The model generates diverse sequences that recapitulate biologically relevant sequence features of natural disordered regions, and we demonstrate that post-training via reinforcement learning with a subcellular localization reward model produces sequences with features which are consistent with known sequence determinants of compartment-specific localization. These results establish IDiom as a general platform for the generative design of intrinsically disordered proteins and regions.

Identifiers

PMID41993527
PMCPMC13082070

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.