HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

A mass spectrometry-based proteomic analysis of Homer2-interacting proteins in the mouse brain.

Abstract
In the brain, the Homer protein family modulates excitatory signal transduction and receptor plasticity through interactions with other proteins in dendritic spines. Homer proteins are implicated in a variety of psychiatric disorders such as schizophrenia and addiction. Since long Homers serve as scaffolding proteins, identifying their interacting partners is an important first step in understanding their biological function and could help to guide the design of new therapeutic strategies. The present study set out to document Homer2-interacting proteins in the mouse brain using a co-immunoprecipitation-based mass spectrometry approach where Homer2 knockout samples were used to filter out non-specific interactors. We found that in the mouse brain, Homer2 interacts with a limited subset of its previously reported interacting partners (3 out of 31). Importantly, we detected an additional 15 novel Homer2-interacting proteins, most of which are part of the N-methyl-D-aspartate receptor signaling pathway. These results corroborate the central role Homer2 plays in glutamatergic transmission and expand the network of proteins potentially contributing to the behavioral abnormalities associated with altered Homer2 expression.
SIGNIFICANCE:
Long Homer proteins are scaffolding proteins that regulate signal transduction in neurons. Identifying their interacting partners is key to understanding their function. We used co-immunoprecipitation in combination with mass spectrometry to establish the first comprehensive list of Homer2-interacting partners in the mouse brain. The specificity of interactions was evaluated using Homer2 knockout brain tissue as a negative control. The set of proteins that we identified minimally overlaps with previously reported interacting partners of Homer2; however, we identified novel interactors that are part of a signaling cascade activated by glutamatergic transmission, which improves our mechanistic understanding of the role of Homer2 in behavior.
AuthorsScott P Goulding, Karen K Szumlinski, Candice Contet, Michael J MacCoss, Christine C Wu
JournalJournal of proteomics (J Proteomics) Vol. 166 Pg. 127-137 (08 23 2017) ISSN: 1876-7737 [Electronic] Netherlands
PMID28728878 (Publication Type: Journal Article, Research Support, N.I.H., Extramural)
CopyrightCopyright © 2017 Elsevier B.V. All rights reserved.
Chemical References
  • Homer Scaffolding Proteins
  • Receptors, N-Methyl-D-Aspartate
Topics
  • Animals
  • Brain (metabolism)
  • Homer Scaffolding Proteins (metabolism)
  • Immunoprecipitation
  • Mass Spectrometry
  • Mice
  • Protein Binding
  • Proteomics
  • Receptors, N-Methyl-D-Aspartate (metabolism)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: