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Real-Time View of Living Cells

Photonics.com
Mar 2010
CAMBRIDGE, Mass. March 17, 2010 – For the first time scientists have recorded real-time microscopic images showing the deadly effects of naturally occurring proteins, called antimicrobial peptides (AMPs), in live bacteria.

Researchers led by Angela Belcher, a professor at Massachusetts Institute of Technology (MIT), modified an existing, extremely sensitive technique known as high-speed atomic force microscopy (AFM) to allow them to image the bacteria in real time. Their method represents the first way to study living cells using high-resolution images recorded in rapid succession.


This image, taken with atomic force microscopy, shows E. coli bacteria after they have been exposed to the antimicrobial peptide CM15. The peptides have begun destroying the bacteria’s cell walls. (Image: Georg Fantner)

Using this type of high-speed AFM could allow scientists to study how cells respond to other drugs and to viral infection, says Belcher, who is the Germeshausen Professor of Materials Science and Engineering and Biological Engineering and a member of the Koch Institute for Integrative Cancer Research at MIT.

It could also be useful in studying cell death in mammalian cells, such as the nerve cell death that occurs in Alzheimer’s patients, according to Paul Hansma, a physics professor at the University of California at Santa Barbara who has been developing AFM technology for 20 years.

“This paper is a highly significant advance in the state-of-the-art imaging of cellular processes,” commented Hansma, who was not involved in the research.

High speed

Atomic force microscopy, invented in 1986, is widely used to image nanoscale materials. Its resolution (about 5 nanometers) is comparable to that of electron microscopy, but unlike electron microscopy, it does not require a vacuum and thus can be used with living samples. However, traditional AFM requires several minutes to produce one image, so it cannot record a sequence of rapidly occurring events.

In recent years, scientists have developed high-speed AFM techniques, but haven’t optimized them for living cells. That’s what the MIT team set out to do, building on the experience of lead author Georg Fantner, a postdoctoral associate in Belcher’s lab who had worked on high-speed AFM at the University of California at Santa Barbara.

Atomic force microscopy makes use of a cantilever equipped with a probe tip that “feels” the surface of a sample. Forces between the tip and the sample can be measured as the probe moves across the sample, revealing the shape of the surface. The MIT team used a cantilever about 1,000 times smaller than those normally used for AFM, which enabled them to increase the imaging speed without harming the bacteria.

The measurements are performed in a liquid environment, another critical factor in keeping the bacteria alive.

With the new setup, the team was able to take images every 13 seconds over a period of several minutes following treatment with an AMP known as CM15. They found that AMP-induced cell death appears to be a two-step process: a short incubation period followed by a rapid “execution.” They were surprised to see that the onset of the incubation period varied from 13 to 80 seconds.

“Not all of the cells started dying at the exact same time, even though they were genetically identical and were exposed to the peptide at the same time,” says Roberto Barbero, a graduate student in biological engineering and a co-author of the paper.

Most AMPs act by puncturing bacterial cell membranes, which destroys the delicate equilibrium between the bacterium and its environment. Others appear to target machinery inside the cell. There has been a great deal of interest in developing AMPs as drugs that could supplement or replace traditional antibiotics, but none have been approved yet.

Until a few years ago, it was thought that bacteria could not become resistant to AMPS, but recent studies have shown that they can. The new MIT work could help researchers understand how that resistance develops.

The research was funded by an Erwin-Schrodinger Fellowship, the National Institutes of Health, Army Research Office and Austrian Research Promotion Agency.

For more information, visit: www.mit.edu


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