G protein-coupled receptors
from structure to function
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Author
Contributions
- Royal Society of Chemistry (Great Britain) - Contributor
Publication
2011 - Royal Society of Chemistry, Cambridge, England
Language
English
Word Count
128,000 words, Guess
Page Count
512 pages
Physical Format
Electronic resource
Identifiers
- Internet Archivegproteincoupledr00gira
- ISBN-101849733449
- ISBN-139781849733441
- OCLC Control Number754110226
- Better World Books9781849733441
and 1 more
- Open LibraryOL27041630M
Classifications
- DDC572.696
- LCCQP552.G16 G77 2011
Alternate Titles
- RSC ebook collection.
Description
G protein-coupled receptors (GPCRs) are the largest family of cell-surface receptors, with more than 800 members identified thus far in the human genome. They regulate the function of most cells in the body, and represent approximately 3% of the genes in the human genome. These receptors respond to a wide variety of structurally diverse ligands, ranging from small molecules, such as biogenic amines, nucleotides and ions, to lipids, peptides, proteins, and even light. Ligands (agonists and antagonists) acting on GPCRs are important in the treatment of numerous diseases, including cardiovascular and mental disorders, retinal degeneration, cancer, and AIDS. It is estimated that these receptors represent about one third of the actual identified targets of clinically used drugs.The determination of rhodopsin crystal structure and, more recently, of opsin, 1 and 2 adrenergic and A2A adenosine receptors provides both academia and industry with extremely valuable data for a better understanding of the molecular determinants of receptor function and a more reliable rationale for drug design. GPCR structure and function constitutes a hot topic.The book, which lies between the fields of chemical biology, molecular pharmacology and medicinal chemistry, is divided into three parts. The first part considers what receptor structures tell us about the mechanism of receptor activation. Part II focuses on receptor function. It discusses what the data from biophysical and mutational studies, and the analysis of the interactions of the receptor with ligands and regulator proteins, tell us about the process of signal transduction. The final part, on modelling and simulation, details new insights on the link between structure and mechanism and their implications in drug design.
Series Statement
- RSC drug discovery
Other Editions
- G protein-coupled receptors: from structure to function
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