Piezo1 Forms Specific, Functionally Important Interactions with Phosphoinositides and Cholesterol
Touch, hearing, and blood pressure regulation require mechanically gated ion channels that convert mechanical stimuli into electrical currents. One such channel is Piezo1, which plays a key role in the transduction of mechanical stimuli in humans and is implicated in diseases, such as xerocytosis an...
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Veröffentlicht in: | Biophysical journal 2020-10, Vol.119 (8), p.1683-1697 |
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creator | Buyan, Amanda Cox, Charles D. Barnoud, Jonathan Li, Jinyuan Chan, Hannah S.M. Martinac, Boris Marrink, Siewert J. Corry, Ben |
description | Touch, hearing, and blood pressure regulation require mechanically gated ion channels that convert mechanical stimuli into electrical currents. One such channel is Piezo1, which plays a key role in the transduction of mechanical stimuli in humans and is implicated in diseases, such as xerocytosis and lymphatic dysplasia. There is building evidence that suggests Piezo1 can be regulated by the membrane environment, with the activity of the channel determined by the local concentration of lipids, such as cholesterol and phosphoinositides. To better understand the interaction of Piezo1 with its environment, we conduct simulations of the protein in a complex mammalian bilayer containing more than 60 different lipid types together with electrophysiology and mutagenesis experiments. We find that the protein alters its local membrane composition, enriching specific lipids and forming essential binding sites for phosphoinositides and cholesterol that are functionally relevant and often related to Piezo1-mediated pathologies. We also identify a number of key structural connections between the propeller and pore domains located close to lipid-binding sites. |
doi_str_mv | 10.1016/j.bpj.2020.07.043 |
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One such channel is Piezo1, which plays a key role in the transduction of mechanical stimuli in humans and is implicated in diseases, such as xerocytosis and lymphatic dysplasia. There is building evidence that suggests Piezo1 can be regulated by the membrane environment, with the activity of the channel determined by the local concentration of lipids, such as cholesterol and phosphoinositides. To better understand the interaction of Piezo1 with its environment, we conduct simulations of the protein in a complex mammalian bilayer containing more than 60 different lipid types together with electrophysiology and mutagenesis experiments. We find that the protein alters its local membrane composition, enriching specific lipids and forming essential binding sites for phosphoinositides and cholesterol that are functionally relevant and often related to Piezo1-mediated pathologies. We also identify a number of key structural connections between the propeller and pore domains located close to lipid-binding sites.</description><identifier>ISSN: 0006-3495</identifier><identifier>EISSN: 1542-0086</identifier><identifier>DOI: 10.1016/j.bpj.2020.07.043</identifier><identifier>PMID: 32949489</identifier><language>eng</language><publisher>CAMBRIDGE: Elsevier Inc</publisher><subject>Anemia, Hemolytic, Congenital ; Animals ; Biophysics ; Cholesterol ; Hydrops Fetalis ; Ion Channels - genetics ; Ion Channels - metabolism ; Life Sciences & Biomedicine ; Mechanotransduction, Cellular ; Mice ; Phosphatidylinositols ; Science & Technology</subject><ispartof>Biophysical journal, 2020-10, Vol.119 (8), p.1683-1697</ispartof><rights>2020 Biophysical Society</rights><rights>Copyright © 2020 Biophysical Society. Published by Elsevier Inc. 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One such channel is Piezo1, which plays a key role in the transduction of mechanical stimuli in humans and is implicated in diseases, such as xerocytosis and lymphatic dysplasia. There is building evidence that suggests Piezo1 can be regulated by the membrane environment, with the activity of the channel determined by the local concentration of lipids, such as cholesterol and phosphoinositides. To better understand the interaction of Piezo1 with its environment, we conduct simulations of the protein in a complex mammalian bilayer containing more than 60 different lipid types together with electrophysiology and mutagenesis experiments. We find that the protein alters its local membrane composition, enriching specific lipids and forming essential binding sites for phosphoinositides and cholesterol that are functionally relevant and often related to Piezo1-mediated pathologies. 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subjects | Anemia, Hemolytic, Congenital Animals Biophysics Cholesterol Hydrops Fetalis Ion Channels - genetics Ion Channels - metabolism Life Sciences & Biomedicine Mechanotransduction, Cellular Mice Phosphatidylinositols Science & Technology |
title | Piezo1 Forms Specific, Functionally Important Interactions with Phosphoinositides and Cholesterol |
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