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Structure and function of GPCRs

Lebon, Guillaume.

Structure and function of GPCRs

Record Type:	Electronic resources : Monograph/item
Title/Author:	Structure and function of GPCRsedited by Guillaume Lebon.
other author:	Lebon, Guillaume.
Published:	Cham :Springer International Publishing :2019.
Description:	xiv, 289 p. :ill., digital ;24 cm.
Contained By:	Springer eBooks
Subject:	G proteinsReceptors.
Online resource:	https://doi.org/10.1007/978-3-030-24591-7
ISBN:	9783030245917$q(electronic bk.)

Structure and function of GPCRs
Structure and function of GPCRs[electronic resource] /edited by Guillaume Lebon. - Cham :Springer International Publishing :2019. - xiv, 289 p. :ill., digital ;24 cm. - Topics in medicinal chemistry,301862-2461 ;. - Topics in medicinal chemistry ;8..

Structures of Non-rhodopsin GPCRs Elucidated Through X-Ray Crystallography -- NMR Spectroscopy for the Characterization of GPCR Energy Landscapes -- Structure and Activation Mechanism of GPCRs -- Structure-Based Discovery of GPCR Ligands from Crystal Structures and Homology Models -- Integration on Ligand and Structure Based Approaches in GPCRs -- Biased Agonist Pharmacochaperones: Small Molecules in the Toolbox for Selectively Modulating GPCR Activity -- Endosomal PTH Receptor Signaling Through cAMP and Its Consequence for Human Medicine -- Structure and Function Studies of GPCRs by Site-Specific Incorporation of Unnatural Amino Acids -- Fluorescent-Based Strategies to Investigate G Protein-Coupled Receptors: Evolution of the Techniques to a Better Understanding -- Modulation of Metabotropic Glutamate Receptors by Orthosteric, Allosteric, and Light-Operated Ligands.

This book introduces readers to the latest advances in G protein-coupled receptor (GPCR) biology. It reviews our current understanding of the structural basis of ligand binding and allosteric mechanisms, following a decade of technological breakthroughs. Several examples of structure-based drug discovery are presented, together with the future challenges involved in designing better drugs that target GPCRs. In turn, the book illustrates the important concept of GPCR biased signaling in physiological contexts, and presents fluorescent- and light-based methodologies frequently used to measure GPCR signaling or to trace their dynamics in cells upon ligand activation. Taken together, the chapters provide an essential overview and toolkit for new scientific investigators who plan to develop GPCR projects. All chapters were written by experts in their respective fields, and share valuable insights and powerful methodologies for the GPCR field.

ISBN: 9783030245917$q(electronic bk.)

Standard No.: 10.1007/978-3-030-24591-7doiSubjects--Topical Terms:

302879
G proteins
--Receptors.

LC Class. No.: QP552.G16 / S778 2019

Dewey Class. No.: 572.6

Structure and function of GPCRs
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505 0 $a Structures of Non-rhodopsin GPCRs Elucidated Through X-Ray Crystallography -- NMR Spectroscopy for the Characterization of GPCR Energy Landscapes -- Structure and Activation Mechanism of GPCRs -- Structure-Based Discovery of GPCR Ligands from Crystal Structures and Homology Models -- Integration on Ligand and Structure Based Approaches in GPCRs -- Biased Agonist Pharmacochaperones: Small Molecules in the Toolbox for Selectively Modulating GPCR Activity -- Endosomal PTH Receptor Signaling Through cAMP and Its Consequence for Human Medicine -- Structure and Function Studies of GPCRs by Site-Specific Incorporation of Unnatural Amino Acids -- Fluorescent-Based Strategies to Investigate G Protein-Coupled Receptors: Evolution of the Techniques to a Better Understanding -- Modulation of Metabotropic Glutamate Receptors by Orthosteric, Allosteric, and Light-Operated Ligands.
520 $a This book introduces readers to the latest advances in G protein-coupled receptor (GPCR) biology. It reviews our current understanding of the structural basis of ligand binding and allosteric mechanisms, following a decade of technological breakthroughs. Several examples of structure-based drug discovery are presented, together with the future challenges involved in designing better drugs that target GPCRs. In turn, the book illustrates the important concept of GPCR biased signaling in physiological contexts, and presents fluorescent- and light-based methodologies frequently used to measure GPCR signaling or to trace their dynamics in cells upon ligand activation. Taken together, the chapters provide an essential overview and toolkit for new scientific investigators who plan to develop GPCR projects. All chapters were written by experts in their respective fields, and share valuable insights and powerful methodologies for the GPCR field.
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