Split-miniSOG for detecting and localizing intracellular protein-protein interactions: application to correlated light and electron microscopy

BOASSA, D.; Lemieux, S. P.; Lev-Ram, V.; Hu, J.; Xiong, Q.; Phan, S.; Mackey, M.; Ramachandra, R.; Adams, S. R.; Tsien, R. Y.; Ellisman, M. H.; Ngo, J. T.

doi:10.1101/423566

bioRxiv · 10.1101/423566

Split-miniSOG for detecting and localizing intracellular protein-protein interactions: application to correlated light and electron microscopy

BOASSA, D.·Lemieux, S. P.·Lev-Ram, V.·Hu, J.·Xiong, Q.·Phan, S.·Mackey, M.·Ramachandra, R.·Adams, S. R.·Tsien, R. Y.·Ellisman, M. H.·Ngo, J. T.

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Abstract

A protein complementation assay (PCA) for detecting and localizing intracellular protein-protein interactions (PPIs) was built by bisection of miniSOG, a fluorescent flavoprotein derived from the light, oxygen, voltage (LOV)-2 domain of Arabidopsis phototropin. When brought together by interacting proteins, the fragments reconstitute a functional reporter that permits tagged protein complexes to be visualized by fluorescence light microscopy (LM), and then by standard as well as \"multicolor\" electron microscopy (EM) imaging methods via the photooxidation of 3-3-diaminobenzidine (DAB) and its lanthanide-conjugated derivatives.

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BOASSA, D., Lemieux, S. P., Lev-Ram, V., Hu, J., Xiong, Q., Phan, S., Mackey, M., Ramachandra, R., Adams, S. R., Tsien, R. Y., Ellisman, M. H., Ngo, J. T.. 2018-09-21. Split-miniSOG for detecting and localizing intracellular protein-protein interactions: application to correlated light and electron microscopy. https://doi.org/10.1101/423566

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