PT  - JOURNAL ARTICLE
AU  - Ning Zhao
AU  - Kouta Kamijo
AU  - Philip D. Fox
AU  - Haruka Oda
AU  - Tatsuya Morisaki
AU  - Yuko Sato
AU  - Hiroshi Kimura
AU  - Timothy J. Stasevich
TI  - A genetically encoded probe for imaging HA-tagged protein translation, localization, and dynamics in living cells and animals
AID  - 10.1101/474668
DP  - 2018 Jan 01
TA  - bioRxiv
PG  - 474668
4099  - http://biorxiv.org/content/early/2018/11/24/474668.short
4100  - http://biorxiv.org/content/early/2018/11/24/474668.full
AB  - To expand the toolbox of imaging in living cells, we have engineered a new single chain variable fragment (scFv) that binds the classic linear HA epitope with high affinity and specificity in vivo. The resulting probe, which we call the HA frankenbody, is capable of lighting up in multiple colors HA-tagged nuclear, cytoplasmic, and membrane proteins in diverse living cell types. The HA frankenbody also enables state-of-the-art single-molecule experiments, which we demonstrate by tracking single mRNA translation dynamics in living U2OS cells and neurons. In combination with the SunTag, we track two mRNA species simultaneously to demonstrate comparative single-molecule studies of translation can now be done with genetically encoded tools alone. Finally, we use the HA frankenbody to precisely quantify the expression of HA tagged proteins in developing zebrafish embryos. The versatility of the HA frankenbody makes it a powerful new tool for imaging protein dynamics in vivo.One-sentence summary A genetically encodable intracellular single-chain variable fragment that selectively binds the HA epitope (YPYDVPDYA) with high affinity in living cells and organisms can be used to quantify HA-tagged protein translation, localization, and dynamics.