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TMEM120A is a coenzyme A-binding membrane protein with structural similarities to ELOVL fatty acid elongase
TMEM120A, also named as TACAN, is a novel membrane protein highly conserved in vertebrates and was recently proposed to be a mechanosensitive channel involved in sensing mechanical pain. Here we present the single-particle cryogenic electron microscopy (cryo-EM) structure of human TMEM120A, which fo...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8376247/ https://www.ncbi.nlm.nih.gov/pubmed/34374645 http://dx.doi.org/10.7554/eLife.71220 |
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author | Xue, Jing Han, Yan Baniasadi, Hamid Zeng, Weizhong Pei, Jimin Grishin, Nick V Wang, Junmei Tu, Benjamin P Jiang, Youxing |
author_facet | Xue, Jing Han, Yan Baniasadi, Hamid Zeng, Weizhong Pei, Jimin Grishin, Nick V Wang, Junmei Tu, Benjamin P Jiang, Youxing |
author_sort | Xue, Jing |
collection | PubMed |
description | TMEM120A, also named as TACAN, is a novel membrane protein highly conserved in vertebrates and was recently proposed to be a mechanosensitive channel involved in sensing mechanical pain. Here we present the single-particle cryogenic electron microscopy (cryo-EM) structure of human TMEM120A, which forms a tightly packed dimer with extensive interactions mediated by the N-terminal coiled coil domain (CCD), the C-terminal transmembrane domain (TMD), and the re-entrant loop between the two domains. The TMD of each TMEM120A subunit contains six transmembrane helices (TMs) and has no clear structural feature of a channel protein. Instead, the six TMs form an α-barrel with a deep pocket where a coenzyme A (CoA) molecule is bound. Intriguingly, some structural features of TMEM120A resemble those of elongase for very long-chain fatty acids (ELOVL) despite the low sequence homology between them, pointing to the possibility that TMEM120A may function as an enzyme for fatty acid metabolism, rather than a mechanosensitive channel. |
format | Online Article Text |
id | pubmed-8376247 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-83762472021-08-20 TMEM120A is a coenzyme A-binding membrane protein with structural similarities to ELOVL fatty acid elongase Xue, Jing Han, Yan Baniasadi, Hamid Zeng, Weizhong Pei, Jimin Grishin, Nick V Wang, Junmei Tu, Benjamin P Jiang, Youxing eLife Structural Biology and Molecular Biophysics TMEM120A, also named as TACAN, is a novel membrane protein highly conserved in vertebrates and was recently proposed to be a mechanosensitive channel involved in sensing mechanical pain. Here we present the single-particle cryogenic electron microscopy (cryo-EM) structure of human TMEM120A, which forms a tightly packed dimer with extensive interactions mediated by the N-terminal coiled coil domain (CCD), the C-terminal transmembrane domain (TMD), and the re-entrant loop between the two domains. The TMD of each TMEM120A subunit contains six transmembrane helices (TMs) and has no clear structural feature of a channel protein. Instead, the six TMs form an α-barrel with a deep pocket where a coenzyme A (CoA) molecule is bound. Intriguingly, some structural features of TMEM120A resemble those of elongase for very long-chain fatty acids (ELOVL) despite the low sequence homology between them, pointing to the possibility that TMEM120A may function as an enzyme for fatty acid metabolism, rather than a mechanosensitive channel. eLife Sciences Publications, Ltd 2021-08-10 /pmc/articles/PMC8376247/ /pubmed/34374645 http://dx.doi.org/10.7554/eLife.71220 Text en © 2021, Xue et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Structural Biology and Molecular Biophysics Xue, Jing Han, Yan Baniasadi, Hamid Zeng, Weizhong Pei, Jimin Grishin, Nick V Wang, Junmei Tu, Benjamin P Jiang, Youxing TMEM120A is a coenzyme A-binding membrane protein with structural similarities to ELOVL fatty acid elongase |
title | TMEM120A is a coenzyme A-binding membrane protein with structural similarities to ELOVL fatty acid elongase |
title_full | TMEM120A is a coenzyme A-binding membrane protein with structural similarities to ELOVL fatty acid elongase |
title_fullStr | TMEM120A is a coenzyme A-binding membrane protein with structural similarities to ELOVL fatty acid elongase |
title_full_unstemmed | TMEM120A is a coenzyme A-binding membrane protein with structural similarities to ELOVL fatty acid elongase |
title_short | TMEM120A is a coenzyme A-binding membrane protein with structural similarities to ELOVL fatty acid elongase |
title_sort | tmem120a is a coenzyme a-binding membrane protein with structural similarities to elovl fatty acid elongase |
topic | Structural Biology and Molecular Biophysics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8376247/ https://www.ncbi.nlm.nih.gov/pubmed/34374645 http://dx.doi.org/10.7554/eLife.71220 |
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