In vivo labeling method using a genetic construct for nanoscale resolution microscopy
- PMID: 19134467
- PMCID: PMC2710050
- DOI: 10.1016/j.bpj.2008.09.032
In vivo labeling method using a genetic construct for nanoscale resolution microscopy
Abstract
We demonstrate beam scanning-stimulated emission depletion microscopy with in vivo labeled cells. A red emitting fluorescent dye is introduced into membrane protein fused to a multifunctional reporter protein (HaloTag, Promega, Madison, WI) in live cells. This approach allows superresolution stimulated emission depletion imaging without the limitations of immunofluorescence-based staining.
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References
-
- Hell S.W., Stelzer E.H.K. Properties of a 4Pi-confocal fluorescence microscope. J. Opt. Soc. Am. A. 1992;9:2159–2166.
-
- Hell S.W., Wichmann J. Breaking the diffraction resolution limit by stimulated emission. Opt. Lett. 1994;19:780–782. - PubMed
-
- Betzig E., Patterson G.H., Sougrat R., Lindwasser O.W., Olenych S. Imaging intracellular fluorescent proteins at nanometer resolution. Science. 2006;313:1642–1645. - PubMed
-
- Willig K.I., Rizzoli S.O., Westphal V., Jahn R., Hell S.W. STED-microscopy reveals that synaptotagmin remains clustered after synaptic vesicle exocytosis. Nature. 2006;440:935–939. - PubMed
-
- Kittel R.J., Wichmann C., Rasse T.M., Fouquet W., Schmidt M. Bruchpilot promotes active zone assembly, Ca2+-channel clustering, and vesicle release. Science. 2006;312:1051–1054. - PubMed
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