Čeština
EnglishCalcium directly regulates phosphatidylinositol 4,5-bisphosphate headgroup conformation and recognition
Bilkova E.*, Pleskot R.*, Rissanen S.*, Sun S.*, Czogalla A., Cwiklik L., Rog T., Vattulainen I., Cremer P.S.‡, Jungwirth P.‡, Coskun Ü.‡. *These authors contributed equally to this work ‡Corresponding authors
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY 139: 4019-4024, 2017
Klíčová slova: PI(4,5)P2, phosphoinositides, Lipid electrostatics, Lipid signaling, Membrane binding, PH domain, calcium, MD simulation, Sum-frequency generation spectroscopy
Abstrakt: 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 with effect with Giant Unilamellar Vesicles (GUVs). 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 re-arrangements. 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.
DOI: 10.1021/jacs.6b11760 Autoři z ÚEB: Roman Pleskot
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY 139: 4019-4024, 2017
Klíčová slova: PI(4,5)P2, phosphoinositides, Lipid electrostatics, Lipid signaling, Membrane binding, PH domain, calcium, MD simulation, Sum-frequency generation spectroscopy
Abstrakt: 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 with effect with Giant Unilamellar Vesicles (GUVs). 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 re-arrangements. 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.
DOI: 10.1021/jacs.6b11760 Autoři z ÚEB: Roman Pleskot