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Kv3.1 channels are crucial for neuronal repolarization and high-frequency action potential firing, particularly in neurons requiring fast signaling and precise timing, such as those involved in auditory processing and fast-spiking interneurons. They are tetrameric structures composed of four pore-forming alpha subunits, each containing six transmembrane helices (S1–S6). Kv3.1 channelopathy has been linked to various human diseases, including epilepsy, developmental delay, and ataxia, making them potential therapeutic targets for neurological diseases.
Modulation of Kv3.1 channel conformation and function
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