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Spy&Go purification of SpyTag-proteins using pseudo-SpyCatcher to access an oligomerization toolbox
Peptide tags are a key resource, introducing minimal change while enabling a consistent process to purify diverse proteins. However, peptide tags often provide minimal benefit post-purification. We previously designed SpyTag, forming an irreversible bond with its protein partner SpyCatcher. SpyTag p...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6465384/ https://www.ncbi.nlm.nih.gov/pubmed/30988307 http://dx.doi.org/10.1038/s41467-019-09678-w |
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author | Khairil Anuar, Irsyad N. A. Banerjee, Anusuya Keeble, Anthony H. Carella, Alberto Nikov, Georgi I. Howarth, Mark |
author_facet | Khairil Anuar, Irsyad N. A. Banerjee, Anusuya Keeble, Anthony H. Carella, Alberto Nikov, Georgi I. Howarth, Mark |
author_sort | Khairil Anuar, Irsyad N. A. |
collection | PubMed |
description | Peptide tags are a key resource, introducing minimal change while enabling a consistent process to purify diverse proteins. However, peptide tags often provide minimal benefit post-purification. We previously designed SpyTag, forming an irreversible bond with its protein partner SpyCatcher. SpyTag provides an easy route to anchor, bridge or multimerize proteins. Here we establish Spy&Go, enabling protein purification using SpyTag. Through rational engineering we generated SpyDock, which captures SpyTag-fusions and allows efficient elution. Spy&Go enabled sensitive purification of SpyTag-fusions from Escherichia coli, giving superior purity than His-tag/nickel-nitrilotriacetic acid. Spy&Go allowed purification of mammalian-expressed, N-terminal, C-terminal or internal SpyTag. As an oligomerization toolbox, we established a panel of SpyCatcher-linked coiled coils, so SpyTag-fusions can be dimerized, trimerized, tetramerized, pentamerized, hexamerized or heptamerized. Assembling oligomers for Death Receptor 5 stimulation, we probed multivalency effects on cancer cell death. Spy&Go, combined with simple oligomerization, should have broad application for exploring multivalency in signaling. |
format | Online Article Text |
id | pubmed-6465384 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-64653842019-04-17 Spy&Go purification of SpyTag-proteins using pseudo-SpyCatcher to access an oligomerization toolbox Khairil Anuar, Irsyad N. A. Banerjee, Anusuya Keeble, Anthony H. Carella, Alberto Nikov, Georgi I. Howarth, Mark Nat Commun Article Peptide tags are a key resource, introducing minimal change while enabling a consistent process to purify diverse proteins. However, peptide tags often provide minimal benefit post-purification. We previously designed SpyTag, forming an irreversible bond with its protein partner SpyCatcher. SpyTag provides an easy route to anchor, bridge or multimerize proteins. Here we establish Spy&Go, enabling protein purification using SpyTag. Through rational engineering we generated SpyDock, which captures SpyTag-fusions and allows efficient elution. Spy&Go enabled sensitive purification of SpyTag-fusions from Escherichia coli, giving superior purity than His-tag/nickel-nitrilotriacetic acid. Spy&Go allowed purification of mammalian-expressed, N-terminal, C-terminal or internal SpyTag. As an oligomerization toolbox, we established a panel of SpyCatcher-linked coiled coils, so SpyTag-fusions can be dimerized, trimerized, tetramerized, pentamerized, hexamerized or heptamerized. Assembling oligomers for Death Receptor 5 stimulation, we probed multivalency effects on cancer cell death. Spy&Go, combined with simple oligomerization, should have broad application for exploring multivalency in signaling. Nature Publishing Group UK 2019-04-15 /pmc/articles/PMC6465384/ /pubmed/30988307 http://dx.doi.org/10.1038/s41467-019-09678-w Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Khairil Anuar, Irsyad N. A. Banerjee, Anusuya Keeble, Anthony H. Carella, Alberto Nikov, Georgi I. Howarth, Mark Spy&Go purification of SpyTag-proteins using pseudo-SpyCatcher to access an oligomerization toolbox |
title | Spy&Go purification of SpyTag-proteins using pseudo-SpyCatcher to access an oligomerization toolbox |
title_full | Spy&Go purification of SpyTag-proteins using pseudo-SpyCatcher to access an oligomerization toolbox |
title_fullStr | Spy&Go purification of SpyTag-proteins using pseudo-SpyCatcher to access an oligomerization toolbox |
title_full_unstemmed | Spy&Go purification of SpyTag-proteins using pseudo-SpyCatcher to access an oligomerization toolbox |
title_short | Spy&Go purification of SpyTag-proteins using pseudo-SpyCatcher to access an oligomerization toolbox |
title_sort | spy&go purification of spytag-proteins using pseudo-spycatcher to access an oligomerization toolbox |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6465384/ https://www.ncbi.nlm.nih.gov/pubmed/30988307 http://dx.doi.org/10.1038/s41467-019-09678-w |
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