Thermal aggregation of immunoglobulin G depending on the charge state of protein–polyelectrolyte complexes DOI

Akira Nomoto,

Kentaro Shiraki

International Journal of Biological Macromolecules, Journal Year: 2025, Volume and Issue: unknown, P. 139500 - 139500

Published: Jan. 1, 2025

Language: Английский

Conformational ensembles of the human intrinsically disordered proteome DOI
Giulio Tesei, Anna Ida Trolle, Nicolas Jonsson

et al.

Nature, Journal Year: 2024, Volume and Issue: 626(8000), P. 897 - 904

Published: Jan. 31, 2024

Language: Английский

Citations

133

Direct prediction of intrinsically disordered protein conformational properties from sequence DOI Creative Commons
Jeffrey M. Lotthammer, Garrett M. Ginell, Daniel Griffith

et al.

Nature Methods, Journal Year: 2024, Volume and Issue: 21(3), P. 465 - 476

Published: Jan. 31, 2024

Abstract Intrinsically disordered regions (IDRs) are ubiquitous across all domains of life and play a range functional roles. While folded generally well described by stable three-dimensional structure, IDRs exist in collection interconverting states known as an ensemble. This structural heterogeneity means that largely absent from the Protein Data Bank, contributing to lack computational approaches predict ensemble conformational properties sequence. Here we combine rational sequence design, large-scale molecular simulations deep learning develop ALBATROSS, deep-learning model for predicting dimensions IDRs, including radius gyration, end-to-end distance, polymer-scaling exponent asphericity, directly sequences at proteome-wide scale. ALBATROSS is lightweight, easy use accessible both locally installable software package point-and-click-style interface via Google Colab notebooks. We first demonstrate applicability our predictors examining generalizability sequence–ensemble relationships IDRs. Then, leverage high-throughput nature characterize sequence-specific biophysical behavior within between proteomes.

Language: Английский

Citations

103

The acidic intrinsically disordered region of the inflammatory mediator HMGB1 mediates fuzzy interactions with CXCL12 DOI Creative Commons
Malisa Vittoria Mantonico, Federica De Leo, Giacomo Quilici

et al.

Nature Communications, Journal Year: 2024, Volume and Issue: 15(1)

Published: Feb. 8, 2024

Abstract Chemokine heterodimers activate or dampen their cognate receptors during inflammation. The CXCL12 chemokine forms with the fully reduced (fr) alarmin HMGB1 a physiologically relevant heterocomplex (frHMGB1•CXCL12) that synergically promotes inflammatory response elicited by G-protein coupled receptor CXCR4. molecular details of complex formation were still elusive. Here we show an integrated structural approach frHMGB1•CXCL12 is fuzzy heterocomplex. Unlike previous assumptions, frHMGB1 and form dynamic equimolar assembly, structured unstructured regions recognizing dimerization surface. We uncover unexpected role acidic intrinsically disordered region (IDR) in its binding to CXCR4 on cell Our work shows interaction diverges from classical rigid heterophilic chemokines dimerization. Simultaneous interference multiple interactions within might offer pharmacological strategies against conditions.

Language: Английский

Citations

18

Prediction of phase separation propensities of disordered proteins from sequence DOI Creative Commons
Sören von Bülow, Giulio Tesei, Kresten Lindorff‐Larsen

et al.

bioRxiv (Cold Spring Harbor Laboratory), Journal Year: 2024, Volume and Issue: unknown

Published: June 3, 2024

Abstract Phase separation is thought to be one possible mechanism governing the selective cellular enrichment of biomolecular constituents for processes such as transcriptional activation, mRNA regulation, and immune signaling. mediated by multivalent interactions biological macromolecules including intrinsically disordered proteins regions (IDRs). Despite considerable advances in experiments, theory simulations, prediction thermodynamics IDR phase behaviour remains challenging. We combined coarse-grained molecular dynamics simulations active learning develop a fast accurate machine model predict free energy saturation concentration directly from sequence. validate using both experimental computational data. apply our all 27,663 IDRs chain length up 800 residues human proteome find that 1,420 these (5%) are predicted undergo homotypic with transfer energies < −2 k B T . use understand relationship between single-chain compaction separation, changes charge-to hydrophobicity-mediated can break symmetry intra-and inter-molecular interactions. also analyse structural preferences at condensate interfaces substantial heterogeneity determined same sequence properties separation. Our work refines established rules relationships features propensities, models will useful interpreting designing experiments on role design specific propensities.

Language: Английский

Citations

18

DNA binding redistributes activation domain ensemble and accessibility in pioneer factor Sox2 DOI Creative Commons
Sveinn Bjarnason, Jordan A. P. McIvor, Andreas Prestel

et al.

Nature Communications, Journal Year: 2024, Volume and Issue: 15(1)

Published: Feb. 16, 2024

Abstract More than 1600 human transcription factors orchestrate the transcriptional machinery to control gene expression and cell fate. Their function is conveyed through intrinsically disordered regions (IDRs) containing activation or repression domains but lacking quantitative structural ensemble models prevents their mechanistic decoding. Here we integrate single-molecule FRET NMR spectroscopy with molecular simulations showing that DNA binding can lead complex changes in IDR accessibility. The C-terminal of pioneer factor Sox2 highly its conformational dynamics are guided by weak dynamic charge interactions folded domain. Both nucleosome induce major rearrangements without affecting affinity. Remarkably, interdomain redistributed leading variable exposure two critical for transcription. Charged intramolecular allowing redistributions may be common necessary sensitive tuning ensembles.

Language: Английский

Citations

17

Splicing regulation through biomolecular condensates and membraneless organelles DOI
Jimena Giudice, Hao Jiang

Nature Reviews Molecular Cell Biology, Journal Year: 2024, Volume and Issue: 25(9), P. 683 - 700

Published: May 21, 2024

Language: Английский

Citations

17

Protein codes promote selective subcellular compartmentalization DOI
Henry R. Kilgore, Itamar Chinn, Peter G. Mikhael

et al.

Science, Journal Year: 2025, Volume and Issue: unknown

Published: Feb. 6, 2025

Cells have evolved mechanisms to distribute ~10 billion protein molecules subcellular compartments where diverse proteins involved in shared functions must assemble. Here, we demonstrate that with share amino acid sequence codes guide them compartment destinations. A language model, ProtGPS, was developed predicts high performance the localization of human excluded from training set. ProtGPS successfully guided generation novel sequences selectively assemble nucleolus. identified pathological mutations change this code and lead altered proteins. Our results indicate contain not only a folding code, but also previously unrecognized governing their distribution compartments.

Language: Английский

Citations

5

Molecular determinants of condensate composition DOI Creative Commons
Alex S. Holehouse, Simon Alberti

Molecular Cell, Journal Year: 2025, Volume and Issue: 85(2), P. 290 - 308

Published: Jan. 1, 2025

Language: Английский

Citations

4

Disordered regions of condensate-promoting proteins have distinct molecular signatures associated with cellular function DOI
Shubham Vashishtha, Benjamin R. Sabari

Journal of Molecular Biology, Journal Year: 2025, Volume and Issue: unknown, P. 168953 - 168953

Published: Jan. 1, 2025

Language: Английский

Citations

3

Structured protein domains enter the spotlight: modulators of biomolecular condensate form and function DOI Creative Commons

Nathaniel Hess,

Jerelle A. Joseph

Trends in Biochemical Sciences, Journal Year: 2025, Volume and Issue: unknown

Published: Jan. 1, 2025

Language: Английский

Citations

3