AI Article Synopsis

  • Proton-activated chloride (PAC) channels play a crucial role in regulating chloride levels and cell death during acidosis, but their modulation mechanisms are not well understood.
  • Research shows that the phosphatidylinositol 4,5-bisphosphate (PI(4,5)P) found in the plasma membrane is crucial for activating these channels, as its depletion significantly reduces PAC currents.
  • Structural simulations indicate that the binding site for PI(4,5)P shifts from the cytosol to the membrane upon activation, revealing a complex interaction that influences PAC channel activity.

Article Abstract

Proton-activated chloride (PAC) channels, ubiquitously expressed in tissues, regulate intracellular Cl levels and cell death following acidosis. However, molecular mechanisms and signaling pathways involved in PAC channel modulation are largely unknown. Herein, we determine that phosphatidylinositol 4,5-bisphosphate [PI(4,5)P] of the plasma membrane inner leaflet is essential for the proton activation of PAC channels. PI(4,5)P depletion by activating phosphatidylinositol 5-phosphatases or G protein-coupled muscarinic receptors substantially inhibits human PAC currents. In excised inside-out patches, PI(4,5)P application to the cytoplasmic side increases the currents. Structural simulation reveals that the putative PI(4,5)P-binding site is localized within the cytosol in resting state but shifts to the cell membrane's inner surface in an activated state and interacts with inner leaflet PI(4,5)P. Alanine neutralization of basic residues near the membrane-cytosol interface of the transmembrane helice 2 significantly attenuates PAC currents. Overall, our study uncovers a modulatory mechanism of PAC channel through inner membrane PI(4,5)P.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11324729PMC
http://dx.doi.org/10.1038/s41467-024-51400-yDOI Listing

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