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TMEM16 scramblases thin the membrane to enable lipid scrambling

TMEM16 scramblases dissipate the plasma membrane lipid asymmetry to activate multiple eukaryotic cellular pathways. Scrambling was proposed to occur with lipid headgroups moving between leaflets through a membrane-spanning hydrophilic groove. Direct information on lipid-groove interactions is lackin...

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Autores principales: Falzone, Maria E., Feng, Zhang, Alvarenga, Omar E., Pan, Yangang, Lee, ByoungCheol, Cheng, Xiaolu, Fortea, Eva, Scheuring, Simon, Accardi, Alessio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9095706/
https://www.ncbi.nlm.nih.gov/pubmed/35562175
http://dx.doi.org/10.1038/s41467-022-30300-z
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author Falzone, Maria E.
Feng, Zhang
Alvarenga, Omar E.
Pan, Yangang
Lee, ByoungCheol
Cheng, Xiaolu
Fortea, Eva
Scheuring, Simon
Accardi, Alessio
author_facet Falzone, Maria E.
Feng, Zhang
Alvarenga, Omar E.
Pan, Yangang
Lee, ByoungCheol
Cheng, Xiaolu
Fortea, Eva
Scheuring, Simon
Accardi, Alessio
author_sort Falzone, Maria E.
collection PubMed
description TMEM16 scramblases dissipate the plasma membrane lipid asymmetry to activate multiple eukaryotic cellular pathways. Scrambling was proposed to occur with lipid headgroups moving between leaflets through a membrane-spanning hydrophilic groove. Direct information on lipid-groove interactions is lacking. We report the 2.3 Å resolution cryogenic electron microscopy structure of the nanodisc-reconstituted Ca(2+)-bound afTMEM16 scramblase showing how rearrangement of individual lipids at the open pathway results in pronounced membrane thinning. Only the groove’s intracellular vestibule contacts lipids, and mutagenesis suggests scrambling does not require specific protein-lipid interactions with the extracellular vestibule. We find scrambling can occur outside a closed groove in thinner membranes and is inhibited in thicker membranes, despite an open pathway. Our results show afTMEM16 thins the membrane to enable scrambling and that an open hydrophilic pathway is not a structural requirement to allow rapid transbilayer movement of lipids. This mechanism could be extended to other scramblases lacking a hydrophilic groove.
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spelling pubmed-90957062022-05-13 TMEM16 scramblases thin the membrane to enable lipid scrambling Falzone, Maria E. Feng, Zhang Alvarenga, Omar E. Pan, Yangang Lee, ByoungCheol Cheng, Xiaolu Fortea, Eva Scheuring, Simon Accardi, Alessio Nat Commun Article TMEM16 scramblases dissipate the plasma membrane lipid asymmetry to activate multiple eukaryotic cellular pathways. Scrambling was proposed to occur with lipid headgroups moving between leaflets through a membrane-spanning hydrophilic groove. Direct information on lipid-groove interactions is lacking. We report the 2.3 Å resolution cryogenic electron microscopy structure of the nanodisc-reconstituted Ca(2+)-bound afTMEM16 scramblase showing how rearrangement of individual lipids at the open pathway results in pronounced membrane thinning. Only the groove’s intracellular vestibule contacts lipids, and mutagenesis suggests scrambling does not require specific protein-lipid interactions with the extracellular vestibule. We find scrambling can occur outside a closed groove in thinner membranes and is inhibited in thicker membranes, despite an open pathway. Our results show afTMEM16 thins the membrane to enable scrambling and that an open hydrophilic pathway is not a structural requirement to allow rapid transbilayer movement of lipids. This mechanism could be extended to other scramblases lacking a hydrophilic groove. Nature Publishing Group UK 2022-05-11 /pmc/articles/PMC9095706/ /pubmed/35562175 http://dx.doi.org/10.1038/s41467-022-30300-z Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Falzone, Maria E.
Feng, Zhang
Alvarenga, Omar E.
Pan, Yangang
Lee, ByoungCheol
Cheng, Xiaolu
Fortea, Eva
Scheuring, Simon
Accardi, Alessio
TMEM16 scramblases thin the membrane to enable lipid scrambling
title TMEM16 scramblases thin the membrane to enable lipid scrambling
title_full TMEM16 scramblases thin the membrane to enable lipid scrambling
title_fullStr TMEM16 scramblases thin the membrane to enable lipid scrambling
title_full_unstemmed TMEM16 scramblases thin the membrane to enable lipid scrambling
title_short TMEM16 scramblases thin the membrane to enable lipid scrambling
title_sort tmem16 scramblases thin the membrane to enable lipid scrambling
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9095706/
https://www.ncbi.nlm.nih.gov/pubmed/35562175
http://dx.doi.org/10.1038/s41467-022-30300-z
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