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02/10/05
-- A novel technology that can test cells in minutes for responses to any
stimulus, including antibiotics, pathogens, toxins, radiation or
chemotherapy, has been developed by scientists at the University at Buffalo.
The paper
describing the sensor will appear in the Feb. 15 issue of Analytical
Chemistry, and currently is available as an "ASAP" article on the American
Chemical Society Web site http://www.chemistry.org.
Susan Z. Hua,
Ph.D., UB assistant professor of mechanical and aerospace engineering and
physiology and biophysics, is the lead researcher.
The
technology is based on the universal connection between cell volume and the
cell environment, or cell volume cytometry. It is particularly useful
because it eliminates the need to culture bacteria to assess their
sensitivity to antibiotics.
"Now, in a
matter of minutes, we can tell if particular antibiotics are active against
specific bacteria," said Frederick Sachs, Ph.D., professor of physiology and
biophysics at UB, co-director of UB's Center for Single Molecule Biophysics
and a coauthor on the paper.
"We have
measured the sensitivity to antibiotics of different strains of E. Coli in
less than 10 minutes at room temperature. We will get results even faster at
higher temperatures."
Hua and her
students created the tiny silicon chip that is the heart of the sensor
chamber in which the cells are encased for testing.
"The new
technique is so sensitive it can detect changes in cell dimensions never
seen before in living cells," she said. "The necessary power can be supplied
even by a watch battery and the sensor is so small it could fit into a
pencil eraser."
Sachs said
the assay can be used on any biological component that is enclosed by a
membrane. "It doesn't have to be cells. We can use lipid bilayer vesicles
containing a single protein, mitochondria, chloroplasts (plant cells) or
cell nuclei, as well as whole cells. We can screen for just about anything."
For example,
this technique could be used to rapidly scan cancer cells obtained from
biopsies to evaluate the effectiveness of chemotherapy or radiation
protocols. The chip has obvious application to measuring toxins relevant to
bioterrorism, Sachs said.
Cell volume
and physiological function are intimately intertwined, the authors note in
their paper. Normal biological activity, such as metabolism, apoptosis
(programmed cell death) or cell division affect cell volume, as does
abnormal activity, such as exposure to toxic agents. Sachs and Hua call the
sensor a "canary on a chip," to highlight its versatility as a first-line
indicator of activity.
There are
many methods used to measure changes in cell volume, said Hua, but
electrical impedance, the resistance to flow of electric current, is the key
to this sensor's simplicity.
Cells are
electrical insulators, she noted. "When immersed in salt water, which
conducts current, the cells displace some of the water and reduce the
electrical current. If cells swell, as commonly would happen in the presence
of a toxin, the resistance would increase and the current would become
smaller, indicating a cellular response."
In addition
to being simple to use, the chip is inexpensive, low power, portable and
provides real-time results, said Sachs. "The assay is applicable to an
enormous number of problems, and is a particularly powerful tool for drug
screening," he noted.
Additional
authors on the study are Daniel A. Ateya, a UB mechanical engineering
student; Philip A. Gottlieb, Ph.D., research associate professor in the UB
Center for Molecular Biology and Immunology, and Steve Besch, Ph.D.,
research assistant professor of physiology and biophysics. The authors have
filed a patent on the technology.
The work was
supported by grants to Hua and Sachs from the National Science Foundation
and the National Institutes of Health, respectively. The microfabrication
was done primarily in the Nanofabrication Facility at Cornell University.
Source: University at
Buffalo
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