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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...

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Detalles Bibliográficos
Autores principales: Wang, Longfei, Chen, Zhenhang, Wu, Hao, Fu, Tian-Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
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).
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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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