TY - JOUR
T1 - A straightforward approach for bioorthogonal labeling of proteins and organelles in live mammalian cells, using a short peptide tag
AU - Segal, Inbar
AU - Nachmias, Dikla
AU - Konig, Andres
AU - Alon, Ariel
AU - Arbely, Eyal
AU - Elia, Natalie
N1 - Funding Information:
The project leading to this application has received funding from the European Research Council (ERC) under the European Union’s Horizon 2020 research.
Publisher Copyright:
© 2020 The Author(s).
PY - 2020/1/14
Y1 - 2020/1/14
N2 - Background: In the high-resolution microscopy era, genetic code expansion (GCE)-based bioorthogonal labeling offers an elegant way for direct labeling of proteins in live cells with fluorescent dyes. This labeling approach is currently not broadly used in live-cell applications, partly because it needs to be adjusted to the specific protein under study. Results: We present a generic, 14-residue long, N-terminal tag for GCE-based labeling of proteins in live mammalian cells. Using this tag, we generated a library of GCE-based organelle markers, demonstrating the applicability of the tag for labeling a plethora of proteins and organelles. Finally, we show that the HA epitope, used as a backbone in our tag, may be substituted with other epitopes and, in some cases, can be completely removed, reducing the tag length to 5 residues. Conclusions: The GCE-tag presented here offers a powerful, easy-to-implement tool for live-cell labeling of cellular proteins with small and bright probes.
AB - Background: In the high-resolution microscopy era, genetic code expansion (GCE)-based bioorthogonal labeling offers an elegant way for direct labeling of proteins in live cells with fluorescent dyes. This labeling approach is currently not broadly used in live-cell applications, partly because it needs to be adjusted to the specific protein under study. Results: We present a generic, 14-residue long, N-terminal tag for GCE-based labeling of proteins in live mammalian cells. Using this tag, we generated a library of GCE-based organelle markers, demonstrating the applicability of the tag for labeling a plethora of proteins and organelles. Finally, we show that the HA epitope, used as a backbone in our tag, may be substituted with other epitopes and, in some cases, can be completely removed, reducing the tag length to 5 residues. Conclusions: The GCE-tag presented here offers a powerful, easy-to-implement tool for live-cell labeling of cellular proteins with small and bright probes.
UR - http://www.scopus.com/inward/record.url?scp=85077853653&partnerID=8YFLogxK
U2 - 10.1186/s12915-019-0708-7
DO - 10.1186/s12915-019-0708-7
M3 - Article
C2 - 31937312
AN - SCOPUS:85077853653
VL - 18
JO - BMC Biology
JF - BMC Biology
SN - 1741-7007
IS - 1
M1 - 5
ER -