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Regulation of α2AR trafficking and signaling by interacting proteins

  • Qin Wang(corresponding author)
    ,
  • Lee E. Limbird
*Corresponding author for this work
  • University of Alabama at Birmingham
    ,
  • Meharry Medical College
Scholary Output:
Contribution to journal
Article
Peer-review

Open access

Abstract

The continuing discovery of new G protein-coupled receptor (GPCR) interacting proteins and clarification of the functional consequences of these interactions has revealed multiple roles for these events. Some of these interactions serve to scaffold GPCRs to particular cellular micro-compartments or to tether them to defined signaling molecules, while other GPCR-protein interactions control GPCR trafficking and the kinetics of GPCR-mediated signaling transduction. This review provides a general overview of the variety of GPCR-protein interactions reported to date, and then focuses on one prototypical GPCR, the α2AR, and the in vitro and in vivo significance of its reciprocal interactions with arrestin and spinophilin. It seems appropriate to recognize the life and career of Arthur Hancock with a summary of studies that both affirm and surprise our preconceived notions of how nature is designed, as his career-long efforts similarly affirmed the complexity of human biology and attempted to surprise pathological changes in that biology with novel, discovery-based therapeutic interventions. Dr. Hancock's love of life, of family, and of commitment to making the world a better place are a model of the life well lived, and truly missed by those who were privileged to know, and thus love, him.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 1135-1145 (11 pages)

Journal (Volume, Issue Number)

Biochemical Pharmacology (Volume 73, Issue 8)

Publication milestones

  • Published - 04/15/2007

Publication status

Published - 04/15/2007

ISSN

0006-2952

Publication IDs

  • Scopus: 33947099861
  • PubMed: 17229402

Publication metrics

Metrics

Fractional count
1
Fractional count
0.50
Fractional count
1
Fractional count
0.50
Fractional count
1
Fractional count
1
Scopus
citations

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Captures
37
Citation count
91

Funding Details

Q.W. is supported by an American Heart Association Scientist Development grant. L.E.L. is supported by National Institutes of Health Grants HL43671 and DK43879.
FundersFunding numbers
NIH
DK43879
NHLBI
R37HL043671
AHA
-