UMass Amherst Physicist, Biologist Develop New Microscope So Powerful It Sees Individual Molecules
January 6, 2010 – AMHERST, Mass. – Researchers are finding that the ability to see very small things—objects 20,000 times thinner than a human hair—can help answer big biological questions. That’s why Jennifer Ross, a University of Massachusetts Amherst physicist, is building a new microscope that achieves super resolution, allowing scientists to see molecules 100 times smaller than are visible using traditional light microscopy.
The image shows the set-up of a new microscope so powerful it can allow researchers to see individual molecules. The picture was taken in the dark in order to better show two lasers (blue and green lights) going into the microscope at right.
Photo credit: UMass Amherst
Ross is particularly interested in using the microscope to determine how a specialized protein called tubulin controls cell division. She and Patricia Wadsworth, a UMass Amherst biologist, were recently awarded a $684,000 grant by the National Institutes of Health through the American Recovery and Reinvestment Act to develop a microscope incorporating two cutting-edge fluorescence techniques that give researchers the ability to observe and track individual protein molecules. UMass Amherst is the second university in the country to use one of these, called Stochastic Optical Reconstruction Microscopy (STORM).
The new microscope, to be built within the next year, will allow much greater precision in identifying objects—such as certain cellular proteins—by letting scientists see them individually and watch their movement in real time. Ross says this will aid virtually all scientific disciplines to help answer important questions from how neurons communicate with each other in the brain to which are the most efficient green energy sources.
Special fluorescent tags used with the new microscope will allow her to see individual molecules that control cell division—working in real time, in living cells. Seeing individual tubulins in their normal environment should give her better insight into how processes they control can go awry. This could contribute to researchers’ understanding of how uncontrolled cell growth can lead to cancer.
Until now, observing individual proteins has involved isolating these proteins from the cells in which they operate. But observing a single molecule plucked out of its natural environment means normal interactions and behaviors are lost. “That’s not how the cell really is,” says Ross.
The first generation of fluorescence proteins (which recently earned discoverers a Nobel Prize) helped to solve this problem by allowing scientists some ability to watch marked proteins interact in real time inside cells. But when many molecules are fluorescently tagged inside a cell, the amount of light they emit prevents observers from seeing what individual proteins are doing because they all fluoresce at once, creating a glare. Tagging all similar proteins in a cell yields an image that’s too blurry to provide useful data.
The new tagging technique used with the microscope solves this problem by adding a “light switch” that allows the researcher to control the fluorescent marker. Instead of being on constantly, fluorescent tags can be individually selected to turn on using small amounts of purple light, allowing each protein to be seen individually. As the physicist explains, when only a small amount of light is used, it acts as a particle rather than a wave and excites only one fluorescently tagged molecule at a time.
Further, fluorescence from these proteins only lasts a few seconds and then goes dark. Another small set of proteins can be turned on with more purple light. Used in this way, the new, more precise microscope can then create a map of the individual proteins, which is captured on a high resolution camera.
The new microscope also solves another major problem associated with the first generation of light microscopes: Images are so blurry that molecules often appear to be 50 times their actual size. This results from the large amount of fluorescence that each tagged protein emits—researchers can’t distinguish between the real object and the fuzzy patch of light that surrounds it. The effect on investigators is much like asking for directions to a particular office and being told only what building it’s in, Ross explains—without an exact location, the answer is not helpful.
The new fluorescence techniques take advantage of the fact that the brightest light emitted by the objects will come from their centers. Ross and colleagues developed a mathematical formula that can fit the shape of a single molecule’s light intensity pattern. This allows a computer to locate the protein’s center within 20 billionths of a meter instead of 200, making the object appear much more like actual size.
Ross summarizes that both the Fluorescence Photoactivated and Localization Microscopy (FPALM) and STORM techniques that she and colleagues are perfecting should allow scientists to see individual molecules by exciting the fluorescent tags with a small amount of light. STORM uses slightly different dyes that can be “tuned” to tag specific molecules. By tagging different proteins with different fluorescent tags, scientists can also observe the dynamics of multiple proteins concurrently, not possible in first generation fluorescence microscopy.
Ross and colleagues are currently looking for a technician to help build and test the microscope over the next two years. Then the UMass Amherst team will share the instrument with their colleagues, who will be able to use it to view their own samples under the new microscope during the grant’s third year. Watch for large-scale photographs of images they capture to appear in public spaces around Amherst as the work progresses. Tours of the Ross laboratory are also available.
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