International Journal of Biological Macromolecules, Journal Year: 2025, Volume and Issue: unknown, P. 139500 - 139500
Published: Jan. 1, 2025
Language: Английский
International Journal of Biological Macromolecules, Journal Year: 2025, Volume and Issue: unknown, P. 139500 - 139500
Published: Jan. 1, 2025
Language: Английский
Nature, Journal Year: 2024, Volume and Issue: 626(8000), P. 897 - 904
Published: Jan. 31, 2024
Language: Английский
Citations
133Nature 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
103Nature 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
18bioRxiv (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
18Nature 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
17Nature Reviews Molecular Cell Biology, Journal Year: 2024, Volume and Issue: 25(9), P. 683 - 700
Published: May 21, 2024
Language: Английский
Citations
17Science, 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
5Molecular Cell, Journal Year: 2025, Volume and Issue: 85(2), P. 290 - 308
Published: Jan. 1, 2025
Language: Английский
Citations
4Journal of Molecular Biology, Journal Year: 2025, Volume and Issue: unknown, P. 168953 - 168953
Published: Jan. 1, 2025
Language: Английский
Citations
3Trends in Biochemical Sciences, Journal Year: 2025, Volume and Issue: unknown
Published: Jan. 1, 2025
Language: Английский
Citations
3