Second harmonic generating (SHG) nanoprobes for in vivo imaging
Abstract
Fluorescence microscopy has profoundly changed cell and molecular biology studies by permitting tagged gene products to be followed as they function and interact. The ability of a fluorescent dye to absorb and emit light of different wavelengths allows it to generate startling contrast that, in the best cases, can permit single molecule detection and tracking. However, in many experimental settings, fluorescent probes fall short of their potential due to dye bleaching, dye signal saturation, and tissue autofluorescence. Here, we demonstrate that second harmonic generating (SHG) nanoprobes can be used for in vivo imaging, circumventing many of the limitations of classical fluorescence probes. Under intense illumination, such as at the focus of a laser-scanning microscope, these SHG nanocrystals convert two photons into one photon of half the wavelength; thus, when imaged by conventional two-photon microscopy, SHG nanoprobes appear to generate a signal with an inverse Stokes shift like a fluorescent dye, but with a narrower emission. Unlike commonly used fluorescent probes, SHG nanoprobes neither bleach nor blink, and the signal they generate does not saturate with increasing illumination intensity. The resulting contrast and detectability of SHG nanoprobes provide unique advantages for molecular imaging of living cells and tissues.
Additional Information
© 2010 by the National Academy of Sciences. Edited by Harry B. Gray, California Institute of Technology, Pasadena, CA, and approved July 1, 2010 (received for review April 9, 2010). Published online before print July 28, 2010. We thank Le Trinh, Luca Caneparo, Thai Truong, Nathan Hodas, and William Dempsey for comments on the manuscript, Willy Supatto and William Dempsey for help with Matlab, David Koos for mouse tail preparation, and Demetri Psaltis for providing functionalized nanoprobes. Research was in part carried out at the Molecular Materials Research Center of the Beckman Institute of the California Institute of Technology. P.P. is supported by a German Science Foundation (Deutsche Forschungsgemeinschaft) Postdoctoral Fellowship. Supported by the Bio-Imaging Center at the California Institute of Technology, the National Human Genome Research Institute Center of Excellence in Genomic Science Grant P50HG004071, and the City of Hope/California Institute of Technology Initiative. Author contributions: P.P. and S.E.F. designed research; P.P. and J.M. performed research; P.P. contributed new reagents/analytic tools; P.P. and D.W. analyzed data; and P.P. and S.E.F. wrote the paper.Attached Files
Published - Pantazis2010p11232P_Natl_Acad_Sci_Usa.pdf
Supplemental Material - SM01.mov
Supplemental Material - SM02.mov
Supplemental Material - SM03.mov
Supplemental Material - pnas.1004748107_SI.pdf
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Additional details
- PMCID
- PMC2930484
- Eprint ID
- 19722
- Resolver ID
- CaltechAUTHORS:20100830-150819965
- Deutsche Forschungsgemeinschaft (DFG)
- Caltech Bio-Imaging Center
- National Human Genome Research Institute
- P50HG004071
- Caltech/City of Hope Biomedical Initiative
- Created
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2010-09-15Created from EPrint's datestamp field
- Updated
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2021-11-08Created from EPrint's last_modified field