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02/15/05 --
UCLA scientists have created a mechanism at the nanoscale to externally
control the function and action of a protein.
"We can switch a protein on
and off, and while we have controlled a specific protein, we believe our
approach will work with virtually any protein," said Giovanni Zocchi,
assistant professor of physics at UCLA, member of the California NanoSystems
Institute and leader of the research effort. "This research has the
potential to start a new approach to protein engineering."
The research, published in
the journal Physical Review Letters, potentially could lead to a new
generation of targeted "smart" pharmaceutical drugs that are active only in
cells where a certain gene is expressed, or a certain DNA sequence is
present, Zocchi said. Such drugs would have reduced side effects. The
research, federally funded by the National Science Foundation, also may lead
to a deeper understanding of proteins' molecular architecture.
Proteins are switched on and
off in living cells by a mechanism called allosteric control; proteins are
regulated by other molecules that bind to their surface, inducing a change
of conformation, or distortion in the shape, of the protein, making the
protein either active or inactive, Zocchi explained.
"We have made an artificial
mechanism of allosteric control based on mechanical tension -- the first
time this has ever been done," Zocchi said. "Potentially, the applications
could be very far-reaching and beneficial if the research continues to
progress well.
"We insert a molecular spring
on the protein, and we can control the stiffness of the spring externally,"
he said. "We chemically string a short piece of DNA around the protein. We
can switch the protein on and off by changing the stiffness of the DNA. We
have made a new molecule, which we can control. By gluing together two
disparate pieces of the cell's molecular machinery, a protein and a piece of
DNA, we have created a spring-loaded protein which can be turned on and
off."
Zocchi's graduate student,
Brian Choi, worked with a transport protein called MBP (maltose binding
protein), expressed in a bacterium. The MBP protein binds and transports a
sugar.
The first applications Zocchi
foresees for the new molecules are as amplified molecular probes. Currently
it is difficult for scientists to study a single live cell and find what
gene it is expressing, but with an amplified molecular probe, in principle
one could inject the probe into a single cell and detect that the cell is
expressing a particular gene, Zocchi said.
An amplified molecular probe
would make it possible to study the individuality of cells, with
applications in stem cell research and the early detection of disease, said
Zocchi, whose laboratory was established in part through start-up funding
from UCLA's Division of Physical Sciences.
"I'm interested in
conformational changes of macromolecules, and in understanding the physical
basis of this allosteric mechanism, which is central to the regulation in
the cell," Zocchi said.
Source: University of California - Los Angeles
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