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Extreme vetting of dopamine receptor oligomerization

  • Wesley B. Asher
    ,
  • Signe Mathiasen
    ,
  • Michael D. Holsey
    ,
  • Steven G. Grinnell
    ,
  • ,
  • Jonathan A. Javitch(corresponding author)
*Corresponding author for this work
Scholary Output:
Chapter in Book/Report/Conference proceeding
Chapter

Abstract

Numerous reports have emerged over the past two decades suggesting that dopamine receptors form dimeric and/or higher-order oligomeric complexes. The existence of these complexes and their functional properties are of significant interest, as they may provide strategies for developing novel therapeutics that selectively target dopamine receptor complexes with the potential for more refined cellular therapeutics and reduced side-effects. However, there is still great debate and controversy surrounding the structural and functional aspects of dopamine receptor oligomers as well as their physiological relevance. Much of the uncertainty stems from the methodologies employed to understand these complexes, which have clear limitations and/or are not yet fully understood. Herein, we provide an overview of the literature focusing mainly on dopamine receptor homomeric complexes and selected dopamine receptor heteromeric complexes with the goal of providing a critical discussion of the methodology and the logic of the scientific inferences in this body of work.

Publication Information

Output type

Scholary Output:
Chapter in Book/Report/Conference proceeding
Chapter

Original language

English (US)

Pages from-to (Number of pages)

Pages 99-127 (29 pages)

Publication milestones

  • Published - 2017

Publication status

Published - 2017

Publisher

Humana Press Inc.

Publication series

  • Publication series name: Receptors
    ISSN (Print): 1048-6909
    ISSN (Electronic): 2524-6488
    Volume: 33

Publication IDs

  • Scopus: 85051712989

Host publication title

Receptors

Publication metrics

Metrics

Scopus
citations
SciVal
FWCI
1.77
SciVal
Author count
6
SciVal
citations
2
SciVal
Paper percentile
44
Fractional count
1
Fractional count
0.17
Fractional count
5
Fractional count
0.83
Fractional count
1
Fractional count
1

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Captures
12
Citation count
5