Novel Allosteric Modulators of G Protein-coupled Receptors

Research output: Contribution to journalReviewResearchpeer-review

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Novel Allosteric Modulators of G Protein-coupled Receptors. / Gentry, Patrick R; Sexton, Patrick M; Christopoulos, Arthur.

In: The Journal of Biological Chemistry, Vol. 290, No. 32, 07.08.2015, p. 19478-88.

Research output: Contribution to journalReviewResearchpeer-review

Harvard

Gentry, PR, Sexton, PM & Christopoulos, A 2015, 'Novel Allosteric Modulators of G Protein-coupled Receptors', The Journal of Biological Chemistry, vol. 290, no. 32, pp. 19478-88. https://doi.org/10.1074/jbc.R115.662759

APA

Gentry, P. R., Sexton, P. M., & Christopoulos, A. (2015). Novel Allosteric Modulators of G Protein-coupled Receptors. The Journal of Biological Chemistry, 290(32), 19478-88. https://doi.org/10.1074/jbc.R115.662759

Vancouver

Gentry PR, Sexton PM, Christopoulos A. Novel Allosteric Modulators of G Protein-coupled Receptors. The Journal of Biological Chemistry. 2015 Aug 7;290(32):19478-88. https://doi.org/10.1074/jbc.R115.662759

Author

Gentry, Patrick R ; Sexton, Patrick M ; Christopoulos, Arthur. / Novel Allosteric Modulators of G Protein-coupled Receptors. In: The Journal of Biological Chemistry. 2015 ; Vol. 290, No. 32. pp. 19478-88.

Bibtex

@article{7f00c46f3ff24b1eb818e1b254f79449,
title = "Novel Allosteric Modulators of G Protein-coupled Receptors",
abstract = "G protein-coupled receptors (GPCRs) are allosteric proteins, because their signal transduction relies on interactions between topographically distinct, yet conformationally linked, domains. Much of the focus on GPCR allostery in the new millennium, however, has been on modes of targeting GPCR allosteric sites with chemical probes due to the potential for novel therapeutics. It is now apparent that some GPCRs possess more than one targetable allosteric site, in addition to a growing list of putative endogenous modulators. Advances in structural biology are also shedding new insights into mechanisms of allostery, although the complexities of candidate allosteric drugs necessitate rigorous biological characterization.",
keywords = "Allosteric Regulation, Allosteric Site/drug effects, Crystallography, X-Ray/history, Drug Design, History, 21st Century, Humans, Ligands, Models, Molecular, Protein Binding, Protein Structure, Tertiary, Receptors, G-Protein-Coupled/agonists, Signal Transduction, Small Molecule Libraries/chemical synthesis, Structure-Activity Relationship",
author = "Gentry, {Patrick R} and Sexton, {Patrick M} and Arthur Christopoulos",
note = "{\circledC} 2015 by The American Society for Biochemistry and Molecular Biology, Inc.",
year = "2015",
month = "8",
day = "7",
doi = "10.1074/jbc.R115.662759",
language = "English",
volume = "290",
pages = "19478--88",
journal = "Journal of Biological Chemistry",
issn = "0021-9258",
publisher = "American Society for Biochemistry and Molecular Biology, Inc.",
number = "32",

}

RIS

TY - JOUR

T1 - Novel Allosteric Modulators of G Protein-coupled Receptors

AU - Gentry, Patrick R

AU - Sexton, Patrick M

AU - Christopoulos, Arthur

N1 - © 2015 by The American Society for Biochemistry and Molecular Biology, Inc.

PY - 2015/8/7

Y1 - 2015/8/7

N2 - G protein-coupled receptors (GPCRs) are allosteric proteins, because their signal transduction relies on interactions between topographically distinct, yet conformationally linked, domains. Much of the focus on GPCR allostery in the new millennium, however, has been on modes of targeting GPCR allosteric sites with chemical probes due to the potential for novel therapeutics. It is now apparent that some GPCRs possess more than one targetable allosteric site, in addition to a growing list of putative endogenous modulators. Advances in structural biology are also shedding new insights into mechanisms of allostery, although the complexities of candidate allosteric drugs necessitate rigorous biological characterization.

AB - G protein-coupled receptors (GPCRs) are allosteric proteins, because their signal transduction relies on interactions between topographically distinct, yet conformationally linked, domains. Much of the focus on GPCR allostery in the new millennium, however, has been on modes of targeting GPCR allosteric sites with chemical probes due to the potential for novel therapeutics. It is now apparent that some GPCRs possess more than one targetable allosteric site, in addition to a growing list of putative endogenous modulators. Advances in structural biology are also shedding new insights into mechanisms of allostery, although the complexities of candidate allosteric drugs necessitate rigorous biological characterization.

KW - Allosteric Regulation

KW - Allosteric Site/drug effects

KW - Crystallography, X-Ray/history

KW - Drug Design

KW - History, 21st Century

KW - Humans

KW - Ligands

KW - Models, Molecular

KW - Protein Binding

KW - Protein Structure, Tertiary

KW - Receptors, G-Protein-Coupled/agonists

KW - Signal Transduction

KW - Small Molecule Libraries/chemical synthesis

KW - Structure-Activity Relationship

U2 - 10.1074/jbc.R115.662759

DO - 10.1074/jbc.R115.662759

M3 - Review

C2 - 26100627

VL - 290

SP - 19478

EP - 19488

JO - Journal of Biological Chemistry

JF - Journal of Biological Chemistry

SN - 0021-9258

IS - 32

ER -

ID: 213599236