A multidisciplinary team coordinated by biologist Stanley Brul of the University of Amsterdam’s Swammerdam Institute for Life Sciences has improved a technique to study live cells in time with the help of fluorescence and rescan confocal microscopy. The technique can be applied to existing microscopy set-ups, making it an easy and cheap solution when higher resolution is needed. The findings were published in Scientific Reports on 24 March.
The invention of confocal microscopy and fluorescent markers has made it possible to study live cells and processes within them. Something that used to be impossible with traditional microscopes. And the possibilities continue to increase, both with the development of even better fluorescent markers and improved microscopy techniques.
A multidisciplinary team of microscopists, image analysis experts, computer modellers, molecular biologists, cell- and microbiologists, led by professor Stanley Brul, has now developed a new technique to improve the resolution and dynamics of microscopy images, so processes within cells can be studied in even more detail. The work was spearheaded by the Van Leeuwenhoek Centre for Advanced Microscopy.
Their solution overcomes two problems of existing techniques. A number of existing techniques require you to make multiple images, which are then merged into one using mathematical calculations. But this makes them sensitive to errors. Another common technique, for which one image scan suffices, uses a high dose of illumination which generates heat and can interfere with the normal physiology of cells. The new technique of Brul’s team smartly combines a known scanning technique with the use of an annulus, overcoming the need of post-calculations and high doses of illumination. The details can be found in their paper in Scientific Reports.
To prove the value of their technique, the team used it to study the germination of spores of the bacterium Bacillus subtilis. The germination, or ‘awakening’, of these spores is triggered by the binding of certain “germinants” to their receptor proteins (that can be fluorescently labelled) at so-called germinosomes. This process is notoriously hard to study, because the spores have very few of these germinosomes and because of autofluorescence of the spore coat. But the team’s new technique managed to overcome these problems, and they were able to perform time-lapse, super-resolution imaging of Bacillus subtilis spore germination.
According to the biologists themselves, their newly developed technique is architecturally less complex compared to other super-resolution microscopic techniques and easy to use. It uses standard preparation protocols and a relatively simple rescan confocal microscope with annular illumunation, and anyone with standard imaging expertise should be able to perform it. This means it could be adopted by any lab in need for higher resolution imaging.
R. M. P . Breedijk, J. Wen, V. Krishnaswami, T. Bernas, E. M. M. Manders, P. Setlow, N. O. E . Vischer & S. Brul; A live-cell super-resolution technique demonstrated by imaging germinosomes in wild-type bacterial spores, in: Nature Scientific Reports, 24 March 2020. DOI: https://doi.org/10.1038/s41598-020-62377-1