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Salt-Induced Transitions in the Conformational Ensembles of Intrinsically Disordered Proteins

Maity, H and Baidya, L and Reddy, G (2022) Salt-Induced Transitions in the Conformational Ensembles of Intrinsically Disordered Proteins. In: Journal of Physical Chemistry B, 126 (32). 5959 -5971.

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Official URL: https://doi.org/10.1021/acs.jpcb.2c03476

Abstract

Salts modulate the behavior of intrinsically disordered proteins (IDPs) and influence the formation of membraneless organelles through liquid-liquid phase separation (LLPS). In low ionic strength solutions, IDP conformations are perturbed by the screening of electrostatic interactions, independent of the salt identity. In this regime, insight into the IDP behavior can be obtained using the theory for salt-induced transitions in charged polymers. However, salt-specific interactions with the charged and uncharged residues, known as the Hofmeister effect, influence IDP behavior in high ionic strength solutions. There is a lack of reliable theoretical models in high salt concentration regimes to predict the salt effect on IDPs. We propose a simulation methodology using a coarse-grained IDP model and experimentally measured water to salt solution transfer free energies of various chemical groups that allowed us to study the salt-specific transitions induced in the IDPs conformational ensemble. We probed the effect of three different monovalent salts on five IDPs belonging to various polymer classes based on charged residue content. We demonstrate that all of the IDPs of different polymer classes behave as self-avoiding walks (SAWs) at physiological salt concentration. In high salt concentrations, the transitions observed in the IDP conformational ensembles are dependent on the salt used and the IDP sequence and composition. Changing the anion with the cation fixed can result in the IDP transition from a SAW-like behavior to a collapsed globule. An important implication of these results is that a suitable salt can be identified to induce condensation of an IDP through LLPS.

Item Type: Journal Article
Publication: Journal of Physical Chemistry B
Publisher: American Chemical Society
Additional Information: The copyright for this article belongs to the Authors.
Keywords: Coarse-grained modeling; Conformations; Ionic strength; Phase separation; Salts, Conformational ensemble; High salt concentration; Induced transitions; Intrinsically disordered proteins; Liquid-liquid phase separation; Low ionic strength; Membraneless; Protein behavior; Salt-induced; Self avoiding walk, Proteins
Department/Centre: Division of Chemical Sciences > Solid State & Structural Chemistry Unit
Date Deposited: 15 Sep 2022 05:57
Last Modified: 15 Sep 2022 05:57
URI: https://eprints.iisc.ac.in/id/eprint/76469

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