PhD at the
“CARS microscopy of biological samples” with Dr Andy Downes
Microscopy of biological samples is of limited use when white light is used. So biologists use fluorescent dyes – which are either added to cells, or they are produced by genes which have been inserted into the DNA. These fluorescently-labelled images, although useful, are limited in their application. Raman spectroscopy is a label-free technique which is similar to infra-red spectroscopy, which excites molecular vibrations. These vibrations occur at different frequencies in different molecules – for example DNA, proteins and lipids. However, Raman spectroscopy is too slow to image live cells.
Coherent anti-Stokes Raman
Scattering (CARS) microscopy
is around 5 orders of magnitude quicker than normal Raman, so images of live
cells can be acquired in a matter of seconds. Very few of these microscopes
exist worldwide, and we have one of the best here in

Left: 212 μm square region of a 20 μm thick sample of cancerous breast tissue. (A)
Differential interference contrast (DIC), (B) CARS tuned to 1662 cm-1
(proteins), (C) two-photon fluorescence (2PEF), (D) second harmonic generation
(SHG), (E) sum frequency generation (SFG). Centre:
2PEF image of anti-cancer drugs in live breast cancer cells – green channel
shows the accumulation of Doxorubicin molecules within the nuclei. Right: CARS image of 1 μm diameter latex spheres digested by (and contained
within) a human macrophage cell, 50 x 35 μm.
Blue maps the CARS signal specific to latex (3054 cm-1). All images
were acquired in 21 seconds.
PhD research programme
The successful candidate will:
We have an extensive suite of biological laboratories, connected to our CARS microscope and Raman spectrometer rooms.
Informal Enquiries to Dr Andy Downes (tel: 0131 651 7072, e-mail: andy.downes@ed.ac.uk)
Closing date: 31 March 2010.
Stipend 2010/11 £13650 tax
free.
Funding is subject to approval by
the