Magnetic resonance imaging (MRI) is a crucial diagnostic tool and an all-around cool technology that creates three-dimensional views of living tissues without being invasive or harming living tissues. But MRI is also limited; while telescopes see further and further into the cosmos and microscopes see smaller and smaller bodies, MRI can only go so small. But now, by blending atomic force microscopy with MRI's 3-D capabilities, MIT researchers are making a 3-D microscope 100 times more powerful than hospital MRI machines.
Traditional hospital MRI works by registering the very weak magnetic signals that come from hydrogen nuclei. A sample is doused with powerful magnetism that aligns the nuclei's magnetic spins, which in turn creates a strong enough signal for the machine to pick up.
The result is a 3-D image of the sample that is unparalleled in medical diagnostics, but there is a catch: In order to create a strong enough signal for the machine's antenna to pick up, traditional MRI requires trillions of atoms to be present in the sample. The best possible resolution is about three millionths of a meter.While that's fine if you're imaging an entire organ, biologists want to image individual cells and even individual proteins. They can do so with electron microscopes, but not without damaging the samples. So researchers began looking for ways to leverage the power of MRI into higher resolution microscopy.
The idea of magnetic resonance force microscopy (MRFM) isn't new: a theoretical physicist named John Sidles proposed the idea in 1991. Since then researchers have struggled to make the idea pay off, and a collaboration between between MIT and IBM has improved the concept to the point that it can now image with resolutions as low as 5-10 nanometers (that's billionths of a meter).
They've done so by attaching the sample to a very small silicon cantilever (100 nanometers wide). A magnetic iron cobalt tip is eased up to the sample until the atomic spins of the atoms come under the iron cobalt's sway, which generates a tiny force on the cantilever. The spins are then flipped over and over again, causing the cantilever to sway repeatedly. A laser creates 2-D images from the displacement of the cantilever, which can be digitally stitched into a 3-D image.
It's not quite electron microscopy but it's very close, and it doesn't damage the living tissue under examination, meaning individual viruses and cells can be examined up close and in 3-D for the first time. Such up-close images of protein structures and cell bodies could teach researchers a lot about disease as well as help them figure out better ways to fight it.
[MIT News]
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Sorry, but that video didn't really make sense. I understood the way it was explained in the article, but from seeing the video, I'm left wondering: huh?
You might be able to get a better idea about what the "slices" of magnetic resonance are doing if you read about how an MRI device works. There's basically one big magnet to align all the spins, but they use a radio frequency "slice" whose wave action flips the spins over. After the wave passes down your body the spins are back-in the large field and they slowly re-align (precess) back-to the large field. The image occurs because some spins (like bone) precess at a different rate than others (like muscle). This signal is inductively detected from many protons, and Sidles' insight was to imagine mechanical detection of a few protons. In the movie, you can see the blue line change shape as it interacts with the spin, which I thought was a pretty-cool effect to illustrate that the information they recover is a change in the wave form. hope that helps! Doug
^ The sample was the cigar-shaped objects in the video, they were attached to the cantilever. The blue object was the magnetic iron cobalt tip. The ball and arrow represented a single atom's spin being affected by the magnetic field of the iron cobalt. I admit, it's tough to figure out at first, but it makes for a good visual in accordance with the article's description of the process.
And a very nice process it is, too! Almost the resolution of an electron microscope, but I'm wondering exactly which kind of electron microscopy it's closer to - scanning or transmission? It sounds like it may have elements of both?