New Possibilities for Multiphoton Microscopy from Carl Zeiss
OPO and simultaneous lasers for LSM 7 series
Mouse, lymphnode, white: Pecam, capsule, Red: mOrange, endothelial cells.
(Specimen courtesy of F. Kiefer, MPI for molecular Biomedicine, Münster, Germany)
May 16, 2012
Multiphoton confocal microscopes from Carl Zeiss now permit the simultaneous use of two NLO lasers or one laser with an optical
parametric oscillator (OPO). Both components are fully integrated and expand the functionality of the multiphoton systems.
In dual laser systems different laser wavelengths simultaneously excite several fluorescent dyes or proteins.
Without time loss, users can image specimens with one wavelength and manipulate them in the multiphoton mode with another.
The automatic free beam adjustment gives the system a high degree of stability and reproducibility and ensures exact overlay
of the two excitation beams. Such dual laser systems are used, above all, in intravital microscopy, e.g. for examining functional
correlations in the brain of a mouse.
An OPO increases the excitation range of multi- photon microscopy to up to 1300 nanometers and therefore covers in particular
the absorption peak of red fluorescent proteins such as mCherry, mPlum and tdTomato. This efficient, long-wave excitation enables
excellent specimen protection. The potentially very high light intensities of the OPO lasers interact with specific structures in
the tissue, leading to a doubling and tripling of the oscillation frequency.
This non-linear effect of frequency doubling (SHG) occurs, for example.
in striated skeletal muscle and collagen. Frequency tripling is especially visible on regions where structures with inconsistent
optical density converge. These include lipid-water boundaries – for example, between membrane and cytoplasm.
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