Modular Ultrafast Sources for Intergrated control
Modular Ultrafast Sourses for Integrated Control (MUSIC) is a joint project which seeks to lead the way in the development of a new generation of ultrafast lasers. By adopting a modular approach for laser design we aim to demonstrate a platform from which lasers can be designed to address a wide range of user-specific requirements. Although vibronic crystals have been deployed widely in ultrashort-pulse lasers the flexibility offered by conventional laser designs is very limited. To remedy this situation we intend to revolutionise cavity design to enable electrical control of the laser output parameters. Progress is expected to lead to a new generation of lasers that can give applications compatibility that far exceeds that available from traditional laser system designs.
This project is being lead by Professor Wilson Sibbett here at the University of St Andrews. Other investigators include Dr Tom Brown (also at St Andrews) Professors Ian White and Richard Penty (Centre for Photonics Systems, University of Cambridge) Professor Martin Dawson FRSE, Dr Stephane Calvez and Dr David Burns (Institute of Photonics, University of Strathclyde). We have put together a research team having complementary expertise and established track records of international excellence in photonics. This project as a whole is managed from St Andrews University but all three research groups undertake interactive research on all aspects of laser development. Further information can be found at the dedicated MUSIC website.
In terms if the research effort taking place at St Andrews, Christopher Leburn, Klaus Metzger and Christine Jappy are the three main researchers working on this project. There research includes the following activites:

The ability to load membrane impermeable substances into cells is of great interest to cell biologists. Optical transfection is one of the few technologies that allows single cells to easily be transfected, without affecting neighbouring cells. The image on the right shows six cells, three of which were transfected with a plasmid encoding for green fluorescent protein (green & blue cells), and three of which that were not. Cells are co-stained with the blue nuclear dye, DAPI, so only the nuclei of untransfected cells are visible. Early transfection work employed a Ti:Sapphire femtosecond pulsed laser using a standard Gaussian beam profile. More recent work has employed the use of a Bessel Beam profile, obviating the need for exact focussing and opening the possibility of a “point-and-shoot” device for the biological community.