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Sequence-Dependent Material Properties of Biomolecular Condensates and their Relation to Dilute Phase Conformations

Material properties of phase-separated biomolecular assemblies, enriched with disordered proteins, dictate their ability to participate in many cellular functions. Despite the significant effort dedicated to understanding how the sequence of the disordered protein drives its phase separation to form...

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Autores principales: Devarajan, Dinesh Sundaravadivelu, Wang, Jiahui, Nikoubashman, Arash, Kim, Young C., Mittal, Jeetain
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10197689/
https://www.ncbi.nlm.nih.gov/pubmed/37215004
http://dx.doi.org/10.1101/2023.05.09.540038
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author Devarajan, Dinesh Sundaravadivelu
Wang, Jiahui
Nikoubashman, Arash
Kim, Young C.
Mittal, Jeetain
author_facet Devarajan, Dinesh Sundaravadivelu
Wang, Jiahui
Nikoubashman, Arash
Kim, Young C.
Mittal, Jeetain
author_sort Devarajan, Dinesh Sundaravadivelu
collection PubMed
description Material properties of phase-separated biomolecular assemblies, enriched with disordered proteins, dictate their ability to participate in many cellular functions. Despite the significant effort dedicated to understanding how the sequence of the disordered protein drives its phase separation to form condensates, little is known about the sequence determinants of condensate material properties. Here, we computationally decipher these relationships for charged disordered proteins using model sequences comprised of glutamic acid and lysine residues as well as naturally occurring sequences of LAF1’s RGG domain and DDX4’s N-terminal domain. We do so by delineating how the arrangement of oppositely charged residues within these sequences influences the dynamical, rheological, and interfacial properties of the condensed phase through equilibrium and non-equilibrium molecular simulations. Our computations yield material properties that are quantitatively comparable with experimentally characterized condensate systems. Interestingly, we find that the material properties of both the model and natural proteins respond similarly to the segregation of charges, despite their very different sequence compositions. Condensates of the highly charge-segregated sequences exhibit slower dynamics than the uniformly charge-patterned sequences, because of their comparatively long-lived molecular contacts between oppositely charged residues. Surprisingly, the molecular interactions within the condensate are highly similar to those within a single-chain for all sequences. Consequently, the condensate material properties of charged disordered proteins are strongly correlated with their dense phase contact dynamics and their single-chain structural properties. Our findings demonstrate the potential to harness the sequence characteristics of disordered proteins for predicting and engineering the material properties of functional condensates, with insights from the dilute phase properties.
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spelling pubmed-101976892023-05-20 Sequence-Dependent Material Properties of Biomolecular Condensates and their Relation to Dilute Phase Conformations Devarajan, Dinesh Sundaravadivelu Wang, Jiahui Nikoubashman, Arash Kim, Young C. Mittal, Jeetain bioRxiv Article Material properties of phase-separated biomolecular assemblies, enriched with disordered proteins, dictate their ability to participate in many cellular functions. Despite the significant effort dedicated to understanding how the sequence of the disordered protein drives its phase separation to form condensates, little is known about the sequence determinants of condensate material properties. Here, we computationally decipher these relationships for charged disordered proteins using model sequences comprised of glutamic acid and lysine residues as well as naturally occurring sequences of LAF1’s RGG domain and DDX4’s N-terminal domain. We do so by delineating how the arrangement of oppositely charged residues within these sequences influences the dynamical, rheological, and interfacial properties of the condensed phase through equilibrium and non-equilibrium molecular simulations. Our computations yield material properties that are quantitatively comparable with experimentally characterized condensate systems. Interestingly, we find that the material properties of both the model and natural proteins respond similarly to the segregation of charges, despite their very different sequence compositions. Condensates of the highly charge-segregated sequences exhibit slower dynamics than the uniformly charge-patterned sequences, because of their comparatively long-lived molecular contacts between oppositely charged residues. Surprisingly, the molecular interactions within the condensate are highly similar to those within a single-chain for all sequences. Consequently, the condensate material properties of charged disordered proteins are strongly correlated with their dense phase contact dynamics and their single-chain structural properties. Our findings demonstrate the potential to harness the sequence characteristics of disordered proteins for predicting and engineering the material properties of functional condensates, with insights from the dilute phase properties. Cold Spring Harbor Laboratory 2023-09-28 /pmc/articles/PMC10197689/ /pubmed/37215004 http://dx.doi.org/10.1101/2023.05.09.540038 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator.
spellingShingle Article
Devarajan, Dinesh Sundaravadivelu
Wang, Jiahui
Nikoubashman, Arash
Kim, Young C.
Mittal, Jeetain
Sequence-Dependent Material Properties of Biomolecular Condensates and their Relation to Dilute Phase Conformations
title Sequence-Dependent Material Properties of Biomolecular Condensates and their Relation to Dilute Phase Conformations
title_full Sequence-Dependent Material Properties of Biomolecular Condensates and their Relation to Dilute Phase Conformations
title_fullStr Sequence-Dependent Material Properties of Biomolecular Condensates and their Relation to Dilute Phase Conformations
title_full_unstemmed Sequence-Dependent Material Properties of Biomolecular Condensates and their Relation to Dilute Phase Conformations
title_short Sequence-Dependent Material Properties of Biomolecular Condensates and their Relation to Dilute Phase Conformations
title_sort sequence-dependent material properties of biomolecular condensates and their relation to dilute phase conformations
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10197689/
https://www.ncbi.nlm.nih.gov/pubmed/37215004
http://dx.doi.org/10.1101/2023.05.09.540038
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