RIM-binding proteins recruit BK-channels to presynaptic release sites adjacent to voltage-gated Ca(2+)-channels

RIM结合蛋白将BK通道募集到与电压门控Ca(2+)通道相邻的突触前释放位点。

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Abstract

The active zone of presynaptic nerve terminals organizes the neurotransmitter release machinery, thereby enabling fast Ca(2+)-triggered synaptic vesicle exocytosis. BK-channels are Ca(2+)-activated large-conductance K(+)-channels that require close proximity to Ca(2+)-channels for activation and control Ca(2+)-triggered neurotransmitter release by accelerating membrane repolarization during action potential firing. How BK-channels are recruited to presynaptic Ca(2+)-channels, however, is unknown. Here, we show that RBPs (for RIM-binding proteins), which are evolutionarily conserved active zone proteins containing SH3- and FN3-domains, directly bind to BK-channels. We find that RBPs interact with RIMs and Ca(2+)-channels via their SH3-domains, but to BK-channels via their FN3-domains. Deletion of RBPs in calyx of Held synapses decreased and decelerated presynaptic BK-currents and depleted BK-channels from active zones. Our data suggest that RBPs recruit BK-channels into a RIM-based macromolecular active zone complex that includes Ca(2+)-channels, synaptic vesicles, and the membrane fusion machinery, thereby enabling tight spatio-temporal coupling of Ca(2+)-influx to Ca(2+)-triggered neurotransmitter release in a presynaptic terminal.

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