The orchestrated recognition of phosphoinositides and concomitant intracellular release of Ca²⁺ is pivotal to almost every aspect of cellular processes, including membrane homeostasis, cell division and growth, vesicle trafficking, as well as secretion. Although Ca²⁺ is known to directly impact phosphoinositide clustering, little is known about the molecular basis for this or its significance in cellular signaling. Here, we study the direct interaction of Ca²⁺ with phosphatidylinositol 4,5-bisphosphate (PI(4,5)P₂), the main lipid marker of the plasma membrane. Electrokinetic potential measurements of PI(4,5)P₂ containing liposomes reveal that Ca²⁺ as well as Mg²⁺ reduce the zeta potential of liposomes to nearly background levels of pure phosphatidylcholine membranes. Strikingly, lipid recognition by the default PI(4,5)P₂ lipid sensor, phospholipase C delta 1 pleckstrin homology domain (PLC δ1-PH), is completely inhibited in the presence of Ca²⁺, while Mg²⁺ has no effect with 100 nm liposomes and modest effect with giant unilamellar vesicles. Consistent with biochemical data, vibrational sum frequency spectroscopy and atomistic molecular dynamics simulations reveal how Ca²⁺ binding to the PI(4,5)P₂ headgroup and carbonyl regions leads to confined lipid headgroup tilting and conformational rearrangements. We rationalize these findings by the ability of calcium to block a highly specific interaction between PLC δ1-PH and PI(4,5)P₂, encoded within the conformational properties of the lipid itself. Our studies demonstrate the possibility that switchable phosphoinositide conformational states can serve as lipid recognition and controlled cell signaling mechanisms.

#	Concept	H-Index	Publications	Citations
1	Medicine	8	8	298
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3	Engineering	2	2	185
4	Health Sciences	1	1	37
5	Social Sciences	1	1	19

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