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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 |