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The ATPase of the phi29 DNA packaging motor is a member of the hexameric AAA+ superfamily

The AAA+ superfamily of proteins is a class of motor ATPases performing a wide range of functions that typically exist as hexamers. The ATPase of phi29 DNA packaging motor has long been a subject of debate in terms of stoichiometry and mechanism of action. Here, we confirmed the stoichiometry of phi...

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Detalles Bibliográficos
Autores principales: Schwartz, Chad, De Donatis, Gian Marco, Fang, Huaming, Guo, Peixuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3700617/
https://www.ncbi.nlm.nih.gov/pubmed/23706809
http://dx.doi.org/10.1016/j.virol.2013.04.004
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author Schwartz, Chad
De Donatis, Gian Marco
Fang, Huaming
Guo, Peixuan
author_facet Schwartz, Chad
De Donatis, Gian Marco
Fang, Huaming
Guo, Peixuan
author_sort Schwartz, Chad
collection PubMed
description The AAA+ superfamily of proteins is a class of motor ATPases performing a wide range of functions that typically exist as hexamers. The ATPase of phi29 DNA packaging motor has long been a subject of debate in terms of stoichiometry and mechanism of action. Here, we confirmed the stoichiometry of phi29 motor ATPase to be a hexamer and provide data suggesting that the phi29 motor ATPase is a member of the classical hexameric AAA+ superfamily. Native PAGE, EMSA, capillary electrophoresis, ATP titration, and binomial distribution assay show that the ATPase is a hexamer. Mutations in the known Walker motifs of the ATPase validated our previous assumptions that the protein exists as another member of this AAA+ superfamily. Our data also supports the finding that the phi29 DNA packaging motor uses a revolution mechanism without rotation or coiling (Schwartz et al., this issue).
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spelling pubmed-37006172013-08-15 The ATPase of the phi29 DNA packaging motor is a member of the hexameric AAA+ superfamily Schwartz, Chad De Donatis, Gian Marco Fang, Huaming Guo, Peixuan Virology Article The AAA+ superfamily of proteins is a class of motor ATPases performing a wide range of functions that typically exist as hexamers. The ATPase of phi29 DNA packaging motor has long been a subject of debate in terms of stoichiometry and mechanism of action. Here, we confirmed the stoichiometry of phi29 motor ATPase to be a hexamer and provide data suggesting that the phi29 motor ATPase is a member of the classical hexameric AAA+ superfamily. Native PAGE, EMSA, capillary electrophoresis, ATP titration, and binomial distribution assay show that the ATPase is a hexamer. Mutations in the known Walker motifs of the ATPase validated our previous assumptions that the protein exists as another member of this AAA+ superfamily. Our data also supports the finding that the phi29 DNA packaging motor uses a revolution mechanism without rotation or coiling (Schwartz et al., this issue). 2013-05-22 2013-08-15 /pmc/articles/PMC3700617/ /pubmed/23706809 http://dx.doi.org/10.1016/j.virol.2013.04.004 Text en https://creativecommons.org/licenses/by-nc-sa/3.0/ Open Access under CC BY-NC-SA 3.0 (https://creativecommons.org/licenses/by-nc-sa/3.0/) license.
spellingShingle Article
Schwartz, Chad
De Donatis, Gian Marco
Fang, Huaming
Guo, Peixuan
The ATPase of the phi29 DNA packaging motor is a member of the hexameric AAA+ superfamily
title The ATPase of the phi29 DNA packaging motor is a member of the hexameric AAA+ superfamily
title_full The ATPase of the phi29 DNA packaging motor is a member of the hexameric AAA+ superfamily
title_fullStr The ATPase of the phi29 DNA packaging motor is a member of the hexameric AAA+ superfamily
title_full_unstemmed The ATPase of the phi29 DNA packaging motor is a member of the hexameric AAA+ superfamily
title_short The ATPase of the phi29 DNA packaging motor is a member of the hexameric AAA+ superfamily
title_sort atpase of the phi29 dna packaging motor is a member of the hexameric aaa+ superfamily
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3700617/
https://www.ncbi.nlm.nih.gov/pubmed/23706809
http://dx.doi.org/10.1016/j.virol.2013.04.004
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