Improving Fluorescence Microscopy with New Technique
- This figure shows the information-rich cellular images made possible by using the newly reported BAMM technique. The 'Original' image shows cells containing multiple fluorescent targets, all having similar colours. This results in a monochrome image. With BAMM, photobleaching rates are colour coded red, green and blue for visualisation, so that each fluorescently labelled structure can be identified even though the fluorophore's native colour information was never used.
A novel technique developed by researchers at the ARC Centre of Excellence for Nanoscale BioPhotonics (CNBP) will help shine new light on biological questions by improving the quality and quantity of information that can be extracted in fluorescence microscopy.
The technique, ‘bleaching-assisted multichannel microscopy’ (BAMM) takes a current longstanding weakness of fluorescence microscopy – photobleaching – and turns it into a strength that improves imaging output by up to three times, with no additional hardwarerequired. Reported in the journal Biomedical Optics Express, BAMM will help researchers gain biological insights into the intricate processes taking place within living cells. This includes the interplay between proteins and molecules which have the potential to impact a wide range of health areas from fertility, to pain, to heart disease and more.
“Fluorescence microscopy is one of the most widely used techniques in biology. This is where light emitting molecules called fluorophores are bound to extremely small cellular targets such as proteins, genetic material or other biomolecules of interest,” says Dr Antony Orth, CNBP Research Fellow at RMIT University and lead author of the research paper.
“When the fluorophore is excited by light from the microscope, it reacts by emitting a specific colour signature. Seeing that colour signature under the microscope helps us view, track and understand the cellular target that the fluorophore has been bound to.” Notably says Dr Orth, you can attach different coloured fluorophores to different cell targets, all in the one sample, to maximise the data and imaging information that is
This traditional approach to fluorescence microscopy is versatile, but there is a major limitation: the visible (or colour) spectrum, where most fluorophores operate, can get crowded. In an ideal experiment, each target should be chosen to have a distinct colour emission, but this becomes increasingly difficult to arrange as the number of targets increases.
“The visible colour spectrum spans a range of 400 nanometres (nm) to 700 nm and only about 200 nm of this range is available for fluorescence colour emission,” explains Dr Orth.
“A typical fluorophore emits over a 50 nm range of the colour spectrum. Dividing 200 nm of the visible spectrum into 50 nm segments means that the colours of the fluorescent emitters begin to blend together when you attempt to squeeze in more than four colours.” “This is generally limiting researchers to four or fewer fluorescent targets in a sample,” says Dr Orth. “Typically, most experiments are even less ambitious, incorporating only two or three targets. The heart of the problem is that only one property of the fluorophore – its colour – is being used for identification.”
To help overcome this limitation, Dr Orth and his co-researchers have developed an innovative technique called ‘bleaching-assisted multichannel microscopy’ (BAMM) to increase their imaging output. “Instead of using colour to differentiate between fluorophores, we use the fourth dimension of time and exploit a phenomenon called photobleaching—the dimming of a collection of fluorophores or pigments under repeated exposure to light,” says Dr Orth.
“Because each type of fluorophore photo-bleaches at a different rate, we can differentiate between fluorophores without using any colour information. We use the rate of photobleaching as the identifier.” “When paired with traditional colour information, this added dimension of photobleaching enables scientists to use 2-3 times more types of fluorescent molecules, all in one sample. This lets us extract far more information from a single investigation.” “Researchers will be able to design more informative tests – for example, highlighting five targets when only two were previously practical. They will no longer have to avoid using
two fluorophores with the same colour, since a difference in photostability alone is enough to distinguish between the two targets,” he says.
Traditionally, the phenomenon of photobleaching (or fading) has been detrimental to the fluorescent microscopy process. This is where high-intensity and ongoing illumination from the microscope permanently destroys a fluorophore’s ability to fluoresce so that imaging of the cell target becomes impossible.
“BAMM transforms photobleaching from a long-standing weakness of fluorescence microscopy into a significant strength to allow increased identification of cellular targets,” says Dr Orth. “BAMM doesn’t require any additional hardware, it’s comparatively simple to do and doesn’t require any specialised sample preparation. It’s an extremely exciting new approach which has the potential to benefit all fluorescence microscopy users and their exploratory science,” he says.
Antony Orth, Richik N. Ghosh, Emma R. Wilson, Timothy Doughney, Hannah Brown, Philipp Reineck, Jeremy G. Thompson, and Brant C. Gibson: Super-multiplexed fluorescence microscopy via photostability contrast, Biomedical Optics Express, Vol. 9, Issue 7, pp. 2943-2954 (2018) doi: 10.1364/BOE.9.002943