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Agonist-selective recruitment of engineered protein probes and of GRK2 by opioid receptors in living...

Agonist-selective recruitment of engineered protein probes and of GRK2 by opioid receptors in living...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_8c895244c98b40adb73cdb12ae8fea95

Agonist-selective recruitment of engineered protein probes and of GRK2 by opioid receptors in living cells

About this item

Full title

Agonist-selective recruitment of engineered protein probes and of GRK2 by opioid receptors in living cells

Publisher

England: eLife Science Publications, Ltd

Journal title

eLife, 2020-02, Vol.9

Language

English

Formats

Publication information

Publisher

England: eLife Science Publications, Ltd

More information

Scope and Contents

Contents

G protein-coupled receptors (GPCRs) signal through allostery, and it is increasingly clear that chemically distinct agonists can produce different receptor-based effects. It has been proposed that agonists selectively promote receptors to recruit one cellular interacting partner over another, introducing allosteric 'bias' into the signaling system....

Alternative Titles

Full title

Agonist-selective recruitment of engineered protein probes and of GRK2 by opioid receptors in living cells

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_8c895244c98b40adb73cdb12ae8fea95

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_8c895244c98b40adb73cdb12ae8fea95

Other Identifiers

ISSN

2050-084X

E-ISSN

2050-084X

DOI

10.7554/eLife.54208

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