NLO Lasers Offer New Possibilities for Multiphoton Microscopy

Both components are integrated and expand the functionality of the multiphoton systems.

An optical parametric oscillator increases the excitation range of multi-photon microscopy to up to 1,300 nanometers and particularly covers 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 nonlinear 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.

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.

The new possibilities for confocal multiphoton microscopy from Carl Zeiss (Jena, Germany) include OPO and simultaneous lasers for the laser-scanning microscope (LSM) 7 series

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