Key result
Removal of the interlinker connecting helix A and helix B of the intracellular C-terminus of Kv7.2 produces a large increase in the number of functional channels at the plasma membrane and increases the steady-state amount of protein.
Removal of the helix A-B linker in Kv7.2 channels increases their surface expression and steady-state protein levels, providing insight into the regulation of neuronal excitability.
Augments Kv7.2 surface expression in vitro; leaves open whether A-B linker targeting modulates excitability in vivo.
Kv7.2 and Kv7.3 are the main components of the neuronal voltage-dependent M-current, which is a subthreshold potassium conductance that exerts an important control on neuronal excitability. Despite their predominantly intracellular distribution, these channels must reach the plasma membrane in order to control neuronal activity. Thus, we analyzed the amino acid sequence of Kv7.2 to identify intrinsic signals that may control its surface expression. Removal of the interlinker connecting helix A and helix B of the intracellular C-terminus produces a large increase in the number of functional channels at the plasma membrane. Moreover, elimination of this linker increased the steady-state amount of protein, which was not associated with a decrease of protein degradation. The magnitude of this increase was inversely correlated with the number of helix A - helix B linkers present in the tetrameric channel assemblies. In contrast to the remarkable effect on the amount of Kv7.2 protein, removal of the Kv7.2 linker had no detectable impact on the steady-state levels of Kv7.3 protein.
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Aivar et al. (2012) studied this question. Removal of the Kv7.2 helix A-B linker vs. Wild-type Kv7.2 was evaluated on Surface expression and steady-state protein levels. Removal of the interlinker connecting helix A and helix B of the intracellular C-terminus of Kv7.2 produces a large increase in the number of functional channels at the plasma membrane and increases the steady-state amount of protein.
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