"Microscopes have to evolve to keep up with the demands of modern science," says Ernst Stelzer, whose group at EMBL developed SPIM. "Molecular biology has graduated upwards from studying single molecules - now we need to watch complex, three-dimensional processes in whole, living organisms. SPIM allows us to do that with unprecedented quality."
In a series of technical innovations, Stelzer and his colleagues (in particular Jim Swoger and Jan Huisken) have made it possible to make three-dimensional films of the inner workings of living organisms at a much higher level of detail than ever before.
One innovation of SPIM is the illumination of a sample from the side rather than along the traditional view of the microscope lens. This eliminates a problem that has plagued three-dimensional microscopy in the past: researchers could obtain excellent resolution in the plane of the microscope slide, but resolution along the direction of the viewer was very fuzzy. In SPIM, a sample is passed through a thin sheet of light, capturing high-quality images layer-by-layer. The sample can be rotated and viewed along different directions, further eliminating the blurry and unwanted light which prevented scientists from looking deep into tissues in the past. The entire procedure is very fast and in a computer supported post-processing step, one or more stacks of images are assembled into a high-resolution film.
Another advantage of SPIM is that the specimen is kept alive in a liquid-filled chamber, allowing scientists to tra
Source:European Molecular Biology Laboratory