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.
Abstract:
Mammalian transient receptor potential canonical (TRPC) genes encode a family of nonselective cation channels that are activated following stimulation of G-protein-coupled membrane receptors linked to phospholipase C. In Drosophila photoreceptor cells, TRP channels are found in large, multimolecular signaling complexes in association with the PDZ-containing scaffolding protein, INAD. A similar mammalian TRPC "signalplex" has been proposed, but has yet to be defined. In the present study, affinity-purified polyclonal antibodies against TRPC5 and TRPC6 were used to immunoprecipitate signalplex components from rat brain lysates. Immunoprecipitated proteins were separated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis, digested with trypsin, and sequenced by mass spectrometry. Proteins identified in the immunoprecipitates included cytoskeletal proteins spectrin, myosin, actin, drebrin, tubulin, and neurabin; endocytic vesicle-associated proteins clathrin, dynamin and AP-2; and the plasmalemmal Na(+)/K(+)-ATPase (NKA) pump. Several of these interactions were confirmed by reciprocal immunoprecipitation followed by Western blot analysis. In lysates from rat kidney, TRPC6, but not TRPC3, was found to coimmunoprecipitate with the NKA pump. Likewise, TRPC6, stably expressed in human embryonic kidney (HEK) cells, coimmunoprecipitated with endogenous NKA and colocalized with the pump to the plasmalemma when examined by immunofluorescence microscopy. Cell surface biotinylation experiments in intact HEK cells, confirmed that both the Na(+) pump and TRPC6 were present in the surface membrane and appeared to interact. Lastly, TRPC6 coimmunoprecipitated with the NKA pump when the proteins were coexpressed in Spodoptera frugiperda insect cells using recombinant baculoviruses. These observations suggest that TRPC6 and the Na(+) pump are part of a functional complex that may be involved in ion transport and homeostasis in both the brain and kidney.
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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