location-svg
Meine Position
Download
The Structural Basis of Arrestin Functions
eBook
eBook
Fachbuch
2017

The Structural Basis of Arrestin Functions

Bewertung abgeben
ISBN
EAN
978-3-319-57553-7
9783319575537
Artikel-Nr.
8VK58Q4
Rabatt
-21.7
%
CHF 189.00
CHF
147.89
Anzahl
1
speech-bubble-svg Beschreibung
This volume summarizes our current understanding of the structural basis of the functions of arrestin family of proteins. Arrestins were first discovered as key players in the desensitization of G protein-coupled receptors (GPCRs). Recent studies showed that arrestins are important signal transducers in their own right, organizing multi-protein complexes and scaffolding numerous signaling cascades that regulate cell proliferation, differentiation, and apoptotic death.

Here arrestin functions are described primarily from the structural prospective. The book covers basal structure of arrestin proteins, receptor binding-induced conformational changes in arrestins, as well as the structure of “pre-activated” mutants. Particular focus is on the arrestin elements interacting with numerous binding partners, GPCRs and cytoplasmic signaling proteins. We expect that this information and insights will help to understand and exploit the phenomenon of signaling bias, which is a new promising direction in drug discovery.
The chapters are written by the world-class specialists in the field, mostly the people who actually contributed the data discussed. The book gives coherent historical prospective and describes the most recent findings.
The book would be particularly useful for scientists in academia and industry working in the fields of pharmacology, cell biology, structural biology, and drug discovery. We expect that the focus on the molecular basis of protein-protein interactions would help to develop novel tools for engaging this important type of targets for research and therapeutic purposes.


feather-svg
Stichwörter
Inhaltsverzeichnis

Arrestins: discovery of the family and functional role of conformational flexibility.- Overview of arrestin-mediated signaling with receptors and non-receptor binding partners.- Initial crystallographic studies of visual arrestin: insights and perspectives.- Structural basis for b-arrestins in GPCR trafficking.- Arrestin-3: the structural basis of lower receptor selectivity.- Phosphate sensor and construction of phosphorylation-independent arrestins.- Comprehensive analysis of the role of arrestin residues in receptor binding.- How arrestin recognizes and binds active GPCRs.- Localization of conformational dynamics of arrestins by HDX-MS.- GPCR footprint on arrestins and manipulation of receptor specificity.- The structure of the polar core mutant R175E and its functional implications.- Active conformations of arrestins: expected and unexpected changes.- The arrestin-receptor complex: exciting answers and new questions.- Scaffolding c-Jun N-terminal kinase cascades: mechanistic insights from the reconstituted arrestin-JNK cascades.- Arrestin-dependent ERK activation and its disruption.- The functional role of the conformational changes in arrestin upon activation.- Is signaling specificity encoded in arrestin conformation?.- Monofunctional elements of multi-functional arrestin proteins.- Arrestins in cell death.

feather-svg
Autor/-in
Herausgegeben von
Biografie
Dr. Gurevich got his PhD in Bioorganic Chemistry at the Shemyakin Institute in Moscow. He studied structure and function of arrestin proteins since he joined the lab of Dr. Benovic as a post-doc in 1991. Dr. Gurevich's studies revealed why arrestins prefer active phosphorylated GPCRs and how they sense receptor-attached phosphates. His lab constructed phosphorylation-independent arrestin mutants and tested their ability to compensate for the defects of GPCR phosphorylation. His lab elucidated the structural basis of arrestin preference for particular GPCRs and constructed the first non-visual arrestins with high receptor specificity. In collaboration with different crystallographers Dr. Gurevich's lab solved the structures of all four vertebrate arrestins in basal conformation and the structure of the arrestin-rhodopsin complex.

Publikation
Schweiz
24.05.2017
Springer Verlag
speech-bubble-svg
Sprache
Englisch
book-svg Format
eBook
PDF
304 Seiten
star-svg
Bewertungen
credit-card-svg Zahlungsarten
payment-einzahlungsschein payment-twint payment-mastercard payment-visa payment-american-express payment-post-finance payment-e-post-finance payment-apple-pay payment-google-pay samsung-pay
Bestellen Sie einfach auf Rechnung oder bezahlen Sie bequem und gebührenfrei mit Twint, Kreditkarte, PostFinance, Apple, Google oder Samsung Pay.
Rückgabe
Kein Rückgaberecht
Bei diesem eBook hat entweder der Verlag (Hersteller) das Rückgaberecht ausgeschlossen oder eine Rückgabe ist aufgrund des Vertriebssystems nicht möglich.
eldar-store-white-svg
S
SPIEGEL Bestseller