Ca²⁺ releases E-Syt1 autoinhibition to couple ER-plasma membrane tethering with lipid transport.

The extended synaptotagmins (E-Syts) are endoplasmic reticulum (ER) proteins that bind the plasma membrane (PM) via C2 domains and transport lipids between them via SMP domains. E-Syt1 tethers and transports lipids in a Ca²⁺-dependent manner, but the role of Ca²⁺ in this regulation is unclear. Of the five C2 domains of E-Syt1, only C2A and C2C contain Ca²⁺-binding sites. Using liposome-based assays, we show that Ca²⁺ binding to C2C promotes E-Syt1-mediated membrane tethering by releasing an inhibition that prevents C2E from interacting with PI(4,5)P₂-rich membranes, as previously suggested by studies in semi-permeabilized cells. Importantly, Ca²⁺ binding to C2A enables lipid transport by releasing a charge-based autoinhibitory interaction between this domain and the SMP domain. Supporting these results, E-Syt1 constructs defective in Ca²⁺ binding in either C2A or C2C failed to rescue two defects in PM lipid homeostasis observed in E-Syts KO cells, delayed diacylglycerol clearance from the PM and impaired Ca²⁺-triggered phosphatidylserine scrambling. Thus, a main effect of Ca²⁺ on E-Syt1 is to reverse an autoinhibited state and to couple membrane tethering with lipid transport.

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