Synchrotron UV Fluorescence Microscopy Uncovers New Probes in Cells and Tissues

Abstract Use of deep ultraviolet (DUV, below 350 nm) fluorescence opens up new possibilities in biology because it does not need external specific probes or labeling but instead allows use of the intrinsic fluorescence that exists for many biomolecules when excited in this wavelength range. Indeed, observation of label free biomolecules or active drugs ensures that the label will not modify the biolocalization or any of its properties. In the past, it has not been easy to accomplish DUV fluorescence imaging due to limited sources and to microscope optics. Two worlds were coexisting: the spectrofluorometric measurements with full spectrum information with DUV excitation, which lacked high-resolution localization, and the microscopic world with very good spatial resolution but poor spectral resolution for which the wavelength range was limited to 350 nm. To combine the advantages of both worlds, we have developed a DUV fluorescence microscope for cell biology coupled to a synchrotron beamline, providing fine tunable excitation from 180 to 600 nm and full spectrum acquired on each point of the image, to study DUV excited fluorescence emitted from nanovolumes directly inside live cells or tissue biopsies.

[1]  B. Wilson,et al.  In Vivo Fluorescence Spectroscopy and Imaging for Oncological Applications , 1998, Photochemistry and photobiology.

[2]  Carol J. Cogswell,et al.  The Specimen Illumination Path and Its Effect on Image Quality , 1995 .

[3]  H. Stübel,et al.  Die Fluoreszenz tierischer Gewebe in ultraviolettem Licht , 1911, Pflüger's Archiv für die gesamte Physiologie des Menschen und der Tiere.

[4]  S. Seeger,et al.  Autofluorescence Detection in Analytical Chemistry and Biochemistry , 2010 .

[5]  Hans C. Gerritsen,et al.  Synchrotron radiation as a light source in confocal microscopy , 1992 .

[6]  Raymond F. Chen Fluorescence Quantum Yields of Tryptophan and Tyrosine , 1967 .

[7]  Daniel Zerbib,et al.  DISCO: a low-energy multipurpose beamline at synchrotron SOLEIL. , 2009, Journal of synchrotron radiation.

[8]  N Ramanujam,et al.  In vivo diagnosis of cervical intraepithelial neoplasia using 337-nm-excited laser-induced fluorescence. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[9]  Rebecca Richards-Kortum,et al.  Understanding the Biological Basis of Autofluorescence Imaging for Oral Cancer Detection: High-Resolution Fluorescence Microscopy in Viable Tissue , 2008, Clinical Cancer Research.

[10]  Fran Adar,et al.  Evolution of Instrumentation for Detection of the Raman Effect as Driven by Available Technologies and by Developing Applications. , 2007 .

[11]  Victor Horodincu,et al.  Nucleic acid and protein mass mapping by live-cell deep-ultraviolet microscopy , 2007, Nature Methods.

[12]  Hans C. Gerritsen,et al.  Micro-Volume Time-Resolved Fluorescence Spectroscopy Using a Confocal Synchrotron Radiation Microscope , 1995 .