Author
Listed:
- Irsyad N. A. Khairil Anuar
(University of Oxford, South Parks Road)
- Anusuya Banerjee
(University of Oxford, South Parks Road)
- Anthony H. Keeble
(University of Oxford, South Parks Road)
- Alberto Carella
(University of Oxford, South Parks Road)
- Georgi I. Nikov
(University of Oxford, South Parks Road)
- Mark Howarth
(University of Oxford, South Parks Road)
Abstract
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.
Suggested Citation
Irsyad N. A. Khairil Anuar & Anusuya Banerjee & Anthony H. Keeble & Alberto Carella & Georgi I. Nikov & Mark Howarth, 2019.
"Spy&Go purification of SpyTag-proteins using pseudo-SpyCatcher to access an oligomerization toolbox,"
Nature Communications, Nature, vol. 10(1), pages 1-13, December.
Handle:
RePEc:nat:natcom:v:10:y:2019:i:1:d:10.1038_s41467-019-09678-w
DOI: 10.1038/s41467-019-09678-w
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