Key result
GFP-tagged Kv1.3 channels displayed gating kinetics virtually indistinguishable from wild-type, whereas GFP-Kv1.4 channels lost fast N-type inactivation.
GFP tagging of Kv channels is a viable tool to monitor their spatiotemporal distribution in living cells, though it alters the fast inactivation mechanism of Kv1.4 channels.
Supports GFP tagging for live-cell Kv1.3 tracking; leaves open utility for Kv1.4 due to disrupted inactivation.
Various types of voltage gated potassium channels (Kv) are responsible for setting the resting potential and shaping the membrane potential waveform in the subcellular domains of neurons. In order to visualize the expression behaviour of recombinant Kv channels, we have fused green fluorescent protein (GFP) to the N-terminal of the alpha subunits Kv1.3 and Kv1.4. In transiently transfected HEK 293 cells the GFP-Kv chimeras localize to the plasma membrane. Whole-cell voltage clamp recordings demonstrate that they form functional potassium channels. Kinetic analysis reveals that the gating kinetics of GFP-Kv1.3 are virtually indistinguishable from those displayed by its wild-type correlate. For GFP-Kv1.4 channels we find that their gating is modified in an expected manner. In response to short depolarizing voltage pulses they do not inactivate, indicating that the attached GFP interferes with the fast N-type inactivation mechanism present in wild type Kv1.4 channels. We suggest that GFP tagging of Kv channels might be a useful tool to monitor the spatiotemporal distribution of recombinant potassium channels expressed in living neurons.
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Kupper Jürgen (1998) studied this question. GFP-tagged Kv1.3 and Kv1.4 channels vs. Wild-type Kv1.3 and Kv1.4 channels was evaluated on Gating kinetics and localization. GFP-tagged Kv1.3 channels displayed gating kinetics virtually indistinguishable from wild-type, whereas GFP-Kv1.4 channels lost fast N-type inactivation.
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