Proteomic analysis of TRPC5- and TRPC6-binding partners reveals interaction with the plasmalemmal Na(+)/K(+)-ATPase

Monu Goel1, William Sinkins, Andrew Keightley

  • 1Department of Physiology and Biophysics, Case Western Reserve University School of Medicine, Cleveland, OH 44106, USA.

Insights

Mammalian TRPC6 channels and the Na+/K+-ATPase pump form a functional complex. This protein interaction is observed in the brain and kidney, suggesting roles in ion transport and homeostasis.

Area of Science:

  • Molecular Biology
  • Cell Biology
  • Neuroscience

Background:

  • Mammalian transient receptor potential canonical (TRPC) genes encode nonselective cation channels.
  • TRPC channels are activated by G-protein-coupled receptors and phospholipase C.
  • TRPC channels form multimolecular signaling complexes, but mammalian TRPC signalplexes remain undefined.

Purpose of the Study:

  • To define the mammalian TRPC signalplex.
  • To investigate the interaction between TRPC channels and the Na+/K+-ATPase (NKA) pump.

Main Methods:

  • Immunoprecipitation using antibodies against TRPC5 and TRPC6 from rat brain lysates.
  • Mass spectrometry to identify co-precipitated proteins.
  • Reciprocal immunoprecipitation and Western blot analysis.
  • Co-immunoprecipitation and immunofluorescence microscopy in HEK cells.
  • Cell surface biotinylation experiments.
  • Co-expression in insect cells using baculoviruses.

Main Results:

  • Proteins identified in TRPC immunoprecipitates included cytoskeletal proteins, endocytic proteins, and the NKA pump.
  • TRPC6 co-immunoprecipitated with the NKA pump in rat kidney lysates.
  • TRPC6 and NKA co-immunoprecipitated and colocalized to the plasma membrane in HEK cells.
  • TRPC6 and NKA were confirmed to be at the cell surface and interacting.

Conclusions:

  • TRPC6 and the Na+/K+-ATPase pump form a functional complex.
  • This complex is present in both brain and kidney.
  • The TRPC6-NKA complex may play a role in ion transport and homeostasis.

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