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Purification of Affinity Tag-free Recombinant Tubulin from Insect Cells

α/β-tubulin heterodimers, which can harbor diverse isotypes and post-translational modifications, polymerize into microtubules that are fundamental to many cellular processes. Due to long-standing challenges in generating recombinant tubulin, however, it has been difficult to examine the properties...

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Detalles Bibliográficos
Autores principales: Ti, Shih-Chieh, Wieczorek, Michal, Kapoor, Tarun M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7416841/
https://www.ncbi.nlm.nih.gov/pubmed/32783031
http://dx.doi.org/10.1016/j.xpro.2019.100011
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author Ti, Shih-Chieh
Wieczorek, Michal
Kapoor, Tarun M.
author_facet Ti, Shih-Chieh
Wieczorek, Michal
Kapoor, Tarun M.
author_sort Ti, Shih-Chieh
collection PubMed
description α/β-tubulin heterodimers, which can harbor diverse isotypes and post-translational modifications, polymerize into microtubules that are fundamental to many cellular processes. Due to long-standing challenges in generating recombinant tubulin, however, it has been difficult to examine the properties of specific tubulin isotypes. Here, we provide a protocol for purifying milligrams of affinity tag-free, isotypically pure recombinant tubulin. Our method can be applicable to any tubulin of interest, opening the door to dissecting how tubulin diversity regulates microtubule function. For complete details on the use and execution of this protocol, please see Ti et al. (2018).
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spelling pubmed-74168412020-08-10 Purification of Affinity Tag-free Recombinant Tubulin from Insect Cells Ti, Shih-Chieh Wieczorek, Michal Kapoor, Tarun M. STAR Protoc Protocol α/β-tubulin heterodimers, which can harbor diverse isotypes and post-translational modifications, polymerize into microtubules that are fundamental to many cellular processes. Due to long-standing challenges in generating recombinant tubulin, however, it has been difficult to examine the properties of specific tubulin isotypes. Here, we provide a protocol for purifying milligrams of affinity tag-free, isotypically pure recombinant tubulin. Our method can be applicable to any tubulin of interest, opening the door to dissecting how tubulin diversity regulates microtubule function. For complete details on the use and execution of this protocol, please see Ti et al. (2018). Elsevier 2020-06-03 /pmc/articles/PMC7416841/ /pubmed/32783031 http://dx.doi.org/10.1016/j.xpro.2019.100011 Text en © 2020. 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
Ti, Shih-Chieh
Wieczorek, Michal
Kapoor, Tarun M.
Purification of Affinity Tag-free Recombinant Tubulin from Insect Cells
title Purification of Affinity Tag-free Recombinant Tubulin from Insect Cells
title_full Purification of Affinity Tag-free Recombinant Tubulin from Insect Cells
title_fullStr Purification of Affinity Tag-free Recombinant Tubulin from Insect Cells
title_full_unstemmed Purification of Affinity Tag-free Recombinant Tubulin from Insect Cells
title_short Purification of Affinity Tag-free Recombinant Tubulin from Insect Cells
title_sort purification of affinity tag-free recombinant tubulin from insect cells
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7416841/
https://www.ncbi.nlm.nih.gov/pubmed/32783031
http://dx.doi.org/10.1016/j.xpro.2019.100011
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