Key result
RACK1 binds to the intracellular COOH-terminal tail of the BK(Ca) channel and alters its biophysical properties, suggesting it forms part of a regulatory complex in vascular smooth muscle.
RACK1 interacts with the BK(Ca) channel and may regulate its function in vascular smooth muscle.
Should not alter clinical vascular management; leaves open RACK1 as BK(Ca) regulator in disease models.
The large conductance calcium-activated potassium channel, or BK(Ca) channel, plays an important feedback role in a variety of physiological processes, including neurotransmitter release and smooth muscle contraction. Some reports have suggested that this channel forms a stable complex with regulators of its function, including several kinases and phosphatases. To further define such signaling complexes, we used the yeast two-hybrid system to screen a human aorta cDNA library for proteins that bind to the BK(Ca) channel's intracellular, COOH-terminal "tail". One of the interactors we identified is the protein receptor for activated C kinase 1 (RACK1). RACK1 is a member of the WD40 protein family, which also includes the G protein beta-subunits. Consistent with an important role in BK(Ca)-channel regulation, RACK1 has been shown to be a scaffolding protein that interacts with a wide variety of signaling molecules, including cSRC and PKC. We have confirmed the interaction between RACK1 and the BK(Ca) channel biochemically with GST pull-down and coimmunoprecipitation experiments. We have observed some co-localization of RACK1 with the BK(Ca) channel in vascular smooth muscle cells with immunocytochemical experiments, and we have found that RACK1 has effects on the BK(Ca) channel's biophysical properties. Thus RACK1 binds to the BK(Ca) channel and it may form part of a BK(Ca)-channel regulatory complex in vascular smooth muscle.
No takes yet. Share an insight, caveat, or question.
Isacson et al. (2006) studied this question. RACK1 interaction with BK(Ca) channel was evaluated on Protein-protein interaction and biophysical effects. RACK1 binds to the intracellular COOH-terminal tail of the BK(Ca) channel and alters its biophysical properties, suggesting it forms part of a regulatory complex in vascular smooth muscle.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: