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Hydration-water and membrane lipids modulate G-protein-coupled receptor activation. / Weerasinghe, Nipuna; Fried, Steven D. E.; Struts, Andrey V.; Perera, Suchithranga M. D. C.; Brown, M.F.

In: Biophysical Journal, Vol. 121, No. 3 S1, 01.02.2022, p. 457A-458A.

Research output: Contribution to journalMeeting Abstractpeer-review

Harvard

Weerasinghe, N, Fried, SDE, Struts, AV, Perera, SMDC & Brown, MF 2022, 'Hydration-water and membrane lipids modulate G-protein-coupled receptor activation', Biophysical Journal, vol. 121, no. 3 S1, pp. 457A-458A. https://doi.org/10.1016/j.bpj.2021.11.494

APA

Weerasinghe, N., Fried, S. D. E., Struts, A. V., Perera, S. M. D. C., & Brown, M. F. (2022). Hydration-water and membrane lipids modulate G-protein-coupled receptor activation. Biophysical Journal, 121(3 S1), 457A-458A. https://doi.org/10.1016/j.bpj.2021.11.494

Vancouver

Weerasinghe N, Fried SDE, Struts AV, Perera SMDC, Brown MF. Hydration-water and membrane lipids modulate G-protein-coupled receptor activation. Biophysical Journal. 2022 Feb 1;121(3 S1):457A-458A. https://doi.org/10.1016/j.bpj.2021.11.494

Author

Weerasinghe, Nipuna ; Fried, Steven D. E. ; Struts, Andrey V. ; Perera, Suchithranga M. D. C. ; Brown, M.F. / Hydration-water and membrane lipids modulate G-protein-coupled receptor activation. In: Biophysical Journal. 2022 ; Vol. 121, No. 3 S1. pp. 457A-458A.

BibTeX

@article{4f3d2f8fcaa84a3892d73809e06edf65,
title = "Hydration-water and membrane lipids modulate G-protein-coupled receptor activation",
abstract = "G-protein-coupled receptors (GPCRs) are responsible for transducing signals across lipid membranes in cells and are the largest family of targets (∼40%) for currently approved drugs. They exist as dynamic conformational ensembles with multiple inactive and active conformational substates described by an energy landscape model. We investigated ways in which the receptor hydration level and lipid bilayer composition influence the activation of the archetypical GPCR rhodopsin by quantifying the shift in the metarhodopsin equilibrium in native and POPC recombinant membranes by different polyethylene glycol osmolyte solutions. Our results show a flood of ∼90 water molecules into the rhodopsin interior during photoactivation, forming a solvent-swollen Meta-II active state. Dehydrating conditions favored inactive Meta-I through the efflux of water from the protein interior, while active Meta-II is favored by increasing bilayer thickness and the monolayer spontaneous curvature. The osmotic effect on the protein is more significant than the effect of the lipid bilayer, and hence the overall equilibrium was generally shifted to Meta-I. By contrast, small osmolytes can penetrate the protein core giving a lower excluded volume and stabilizing the Meta-II state. The metarhodopsin equilibrium was furthur shifted towards the Meta-I state in POPC recombinant membranes compared to the native lipid membrane environment. The POPC lipid membrane has zero-spontaneous curvature that shifts the equilibrium towards the more compact, inactive Meta-I state. By contrast, the native lipid membrane environment has a negative spontaneous curvature that favors the more expanded state of Meta-II. Analysis of transducin C-terminal peptide-binding isotherms revealed that the binding affinity is significantly decreased when the lipid environment is changed from the native lipids to POPC lipids. Our results delineate the crucial role of soft matter in regulating the activation process of GPCRs in a membrane lipid environment.",
author = "Nipuna Weerasinghe and Fried, {Steven D. E.} and Struts, {Andrey V.} and Perera, {Suchithranga M. D. C.} and M.F. Brown",
year = "2022",
month = feb,
day = "1",
doi = "10.1016/j.bpj.2021.11.494",
language = "English",
volume = "121",
pages = "457A--458A",
journal = "Biophysical Journal",
issn = "0006-3495",
publisher = "Cell Press",
number = "3 S1",
note = "null ; Conference date: 19-02-2022 Through 23-02-2022",

}

RIS

TY - JOUR

T1 - Hydration-water and membrane lipids modulate G-protein-coupled receptor activation

AU - Weerasinghe, Nipuna

AU - Fried, Steven D. E.

AU - Struts, Andrey V.

AU - Perera, Suchithranga M. D. C.

AU - Brown, M.F.

PY - 2022/2/1

Y1 - 2022/2/1

N2 - G-protein-coupled receptors (GPCRs) are responsible for transducing signals across lipid membranes in cells and are the largest family of targets (∼40%) for currently approved drugs. They exist as dynamic conformational ensembles with multiple inactive and active conformational substates described by an energy landscape model. We investigated ways in which the receptor hydration level and lipid bilayer composition influence the activation of the archetypical GPCR rhodopsin by quantifying the shift in the metarhodopsin equilibrium in native and POPC recombinant membranes by different polyethylene glycol osmolyte solutions. Our results show a flood of ∼90 water molecules into the rhodopsin interior during photoactivation, forming a solvent-swollen Meta-II active state. Dehydrating conditions favored inactive Meta-I through the efflux of water from the protein interior, while active Meta-II is favored by increasing bilayer thickness and the monolayer spontaneous curvature. The osmotic effect on the protein is more significant than the effect of the lipid bilayer, and hence the overall equilibrium was generally shifted to Meta-I. By contrast, small osmolytes can penetrate the protein core giving a lower excluded volume and stabilizing the Meta-II state. The metarhodopsin equilibrium was furthur shifted towards the Meta-I state in POPC recombinant membranes compared to the native lipid membrane environment. The POPC lipid membrane has zero-spontaneous curvature that shifts the equilibrium towards the more compact, inactive Meta-I state. By contrast, the native lipid membrane environment has a negative spontaneous curvature that favors the more expanded state of Meta-II. Analysis of transducin C-terminal peptide-binding isotherms revealed that the binding affinity is significantly decreased when the lipid environment is changed from the native lipids to POPC lipids. Our results delineate the crucial role of soft matter in regulating the activation process of GPCRs in a membrane lipid environment.

AB - G-protein-coupled receptors (GPCRs) are responsible for transducing signals across lipid membranes in cells and are the largest family of targets (∼40%) for currently approved drugs. They exist as dynamic conformational ensembles with multiple inactive and active conformational substates described by an energy landscape model. We investigated ways in which the receptor hydration level and lipid bilayer composition influence the activation of the archetypical GPCR rhodopsin by quantifying the shift in the metarhodopsin equilibrium in native and POPC recombinant membranes by different polyethylene glycol osmolyte solutions. Our results show a flood of ∼90 water molecules into the rhodopsin interior during photoactivation, forming a solvent-swollen Meta-II active state. Dehydrating conditions favored inactive Meta-I through the efflux of water from the protein interior, while active Meta-II is favored by increasing bilayer thickness and the monolayer spontaneous curvature. The osmotic effect on the protein is more significant than the effect of the lipid bilayer, and hence the overall equilibrium was generally shifted to Meta-I. By contrast, small osmolytes can penetrate the protein core giving a lower excluded volume and stabilizing the Meta-II state. The metarhodopsin equilibrium was furthur shifted towards the Meta-I state in POPC recombinant membranes compared to the native lipid membrane environment. The POPC lipid membrane has zero-spontaneous curvature that shifts the equilibrium towards the more compact, inactive Meta-I state. By contrast, the native lipid membrane environment has a negative spontaneous curvature that favors the more expanded state of Meta-II. Analysis of transducin C-terminal peptide-binding isotherms revealed that the binding affinity is significantly decreased when the lipid environment is changed from the native lipids to POPC lipids. Our results delineate the crucial role of soft matter in regulating the activation process of GPCRs in a membrane lipid environment.

UR - https://www.mendeley.com/catalogue/dffbd5b8-7e1c-3018-b566-09561a3f3d75/

U2 - 10.1016/j.bpj.2021.11.494

DO - 10.1016/j.bpj.2021.11.494

M3 - Meeting Abstract

VL - 121

SP - 457A-458A

JO - Biophysical Journal

JF - Biophysical Journal

SN - 0006-3495

IS - 3 S1

Y2 - 19 February 2022 through 23 February 2022

ER -

ID: 97520562