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Targeting Trafficking in Drug Development

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Cover of 'Targeting Trafficking in Drug Development'

Table of Contents

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    Book Overview
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    Chapter 49 Intracellular Trafficking of Gonadotropin Receptors in Health and Disease
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    Chapter 50 Pharmacological Chaperones as Potential Therapeutic Strategies for Misfolded Mutant Vasopressin Receptors
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    Chapter 55 Natural (and Unnatural) Small Molecules as Pharmacological Chaperones and Inhibitors in Cancer
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    Chapter 57 Investigating Internalization and Intracellular Trafficking of GPCRs: New Techniques and Real-Time Experimental Approaches
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    Chapter 59 Folding Defects Leading to Primary Hyperoxaluria
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    Chapter 60 Targeting of Disordered Proteins by Small Molecules in Neurodegenerative Diseases
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    Chapter 62 The Molecular Physiopathogenesis of Islet Amyloidosis
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    Chapter 64 Pharmacoperones for Misfolded Gonadotropin Receptors
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    Chapter 65 Conserved Oligomeric Golgi and Neuronal Vesicular Trafficking
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    Chapter 67 Heritable Skeletal Disorders Arising from Defects in Processing and Transport of Type I Procollagen from the ER: Perspectives on Possible Therapeutic Approaches
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    Chapter 68 Pharmacological Chaperones: Beyond Conformational Disorders
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    Chapter 71 SLC6 Transporter Folding Diseases and Pharmacochaperoning
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    Chapter 72 Potential Pharmacological Chaperones for Cystathionine Beta-Synthase-Deficient Homocystinuria
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    Chapter 103 Cystic Fibrosis, Cystic Fibrosis Transmembrane Conductance Regulator and Drugs: Insights from Cellular Trafficking
Attention for Chapter 57: Investigating Internalization and Intracellular Trafficking of GPCRs: New Techniques and Real-Time Experimental Approaches
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Chapter title
Investigating Internalization and Intracellular Trafficking of GPCRs: New Techniques and Real-Time Experimental Approaches
Chapter number 57
Book title
Targeting Trafficking in Drug Development
Published in
Handbook of experimental pharmacology, January 2017
DOI 10.1007/164_2017_57
Pubmed ID
Book ISBNs
978-3-31-974163-5, 978-3-31-974164-2
Authors

Simon R. Foster, Hans Bräuner-Osborne, Foster, Simon R., Bräuner-Osborne, Hans

Abstract

The ability to regulate the interaction between cells and their extracellular environment is essential for the maintenance of appropriate physiological function. For G protein-coupled receptors (GPCRs), this regulation occurs through multiple mechanisms that provide spatial and temporal control for signal transduction. One of the major mechanisms for GPCR regulation involves their endocytic trafficking, which serves to internalize the receptors from the plasma membrane and thereby attenuate G protein-dependent signaling. However, there is accumulating evidence to suggest that GPCRs can signal independently of G proteins, as well as from intracellular compartments including endosomes. It is in this context that receptor internalization and intracellular trafficking have attracted renewed interest within the GPCR field. In this chapter, we will review the current understanding and methodologies that have been used to investigate internalization and intracellular signaling of GPCRs, with a particular focus on emerging real-time techniques. These recent developments have improved our understanding of the complexities of GPCR internalization and intracellular signaling and suggest that the broader biological relevance and potential therapeutic implications of these processes remain to be explored.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 61 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 61 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 20 33%
Student > Bachelor 9 15%
Other 5 8%
Student > Master 5 8%
Researcher 4 7%
Other 5 8%
Unknown 13 21%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 20 33%
Pharmacology, Toxicology and Pharmaceutical Science 8 13%
Agricultural and Biological Sciences 8 13%
Medicine and Dentistry 3 5%
Engineering 2 3%
Other 5 8%
Unknown 15 25%