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Purification and cryoelectron microscopy structure determination of human V-ATPase
Vesicular- or vacuolar-type adenosine triphosphatases (V-ATPases) are multi-component, ATP-driven proton pumps, which play important roles in many physiological processes by acidifying intracellular vesicles, organelles, and the extracellular milieu. Long-standing challenges in purifying mammalian V...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7902551/ https://www.ncbi.nlm.nih.gov/pubmed/33665630 http://dx.doi.org/10.1016/j.xpro.2021.100350 |
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author | Wang, Longfei Chen, Zhenhang Wu, Hao Fu, Tian-Min |
author_facet | Wang, Longfei Chen, Zhenhang Wu, Hao Fu, Tian-Min |
author_sort | Wang, Longfei |
collection | PubMed |
description | Vesicular- or vacuolar-type adenosine triphosphatases (V-ATPases) are multi-component, ATP-driven proton pumps, which play important roles in many physiological processes by acidifying intracellular vesicles, organelles, and the extracellular milieu. Long-standing challenges in purifying mammalian V-ATPases have limited the biochemical and structural study of mammalian V-ATPase. Here, we provide a protocol for purifying milligrams of human V-ATPase and detail procedures for the reconstruction of its structure by cryo-EM. Our method can be applied to any biochemical and biophysical study of human V-ATPase. For complete details on the use and execution of this protocol, please refer to Wang et al. (2020). |
format | Online Article Text |
id | pubmed-7902551 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-79025512021-03-03 Purification and cryoelectron microscopy structure determination of human V-ATPase Wang, Longfei Chen, Zhenhang Wu, Hao Fu, Tian-Min STAR Protoc Protocol Vesicular- or vacuolar-type adenosine triphosphatases (V-ATPases) are multi-component, ATP-driven proton pumps, which play important roles in many physiological processes by acidifying intracellular vesicles, organelles, and the extracellular milieu. Long-standing challenges in purifying mammalian V-ATPases have limited the biochemical and structural study of mammalian V-ATPase. Here, we provide a protocol for purifying milligrams of human V-ATPase and detail procedures for the reconstruction of its structure by cryo-EM. Our method can be applied to any biochemical and biophysical study of human V-ATPase. For complete details on the use and execution of this protocol, please refer to Wang et al. (2020). Elsevier 2021-02-16 /pmc/articles/PMC7902551/ /pubmed/33665630 http://dx.doi.org/10.1016/j.xpro.2021.100350 Text en © 2021 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Protocol Wang, Longfei Chen, Zhenhang Wu, Hao Fu, Tian-Min Purification and cryoelectron microscopy structure determination of human V-ATPase |
title | Purification and cryoelectron microscopy structure determination of human V-ATPase |
title_full | Purification and cryoelectron microscopy structure determination of human V-ATPase |
title_fullStr | Purification and cryoelectron microscopy structure determination of human V-ATPase |
title_full_unstemmed | Purification and cryoelectron microscopy structure determination of human V-ATPase |
title_short | Purification and cryoelectron microscopy structure determination of human V-ATPase |
title_sort | purification and cryoelectron microscopy structure determination of human v-atpase |
topic | Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7902551/ https://www.ncbi.nlm.nih.gov/pubmed/33665630 http://dx.doi.org/10.1016/j.xpro.2021.100350 |
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