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RESEARCH
Science
Chemistry
CHEMISTRY
Laser technique examines movement in nucleus of
living cell
James
E. Kloeppel, Physical Sciences Editor
(217) 244-1073; kloeppel@uiuc.edu
9/1/2001
CHAMPAIGN, Ill. By
colliding two laser beams head-on, scientists at the University of Illinois
can measure the movement of chromatin (tiny packets of DNA) in the nucleus
of a living cell.
"DNA, in the form of chromatin, plays a key role in several important
chemical reactions that occur in living cells," said Christopher
Bardeen, a UI professor of chemistry. "Understanding how chromatin
motility affects reactions, like the transcription of DNA into RNA for
the production of proteins, is essential to extending our knowledge
in such areas as cell reproduction, embryology and genetic engineering."
While scientists understand how chemical reactions work in a simple
test tube, the dense environment in a living cell presents a far more
complicated system.
"A living cell is a very complex reaction vessel, crowded with
proteins and other large molecules that must move around and interact,"
Bardeen said. "If we try to take a cell apart and examine its constituents,
we find they no longer behave as they do in intact, living cells."
To non-invasively measure chromatin movement in a live frog skin cell,
Bardeen and graduate students Sara Davis and Andrew Stout combine a
two-photon laser fluorescence technique with a standing-wave, counter-propagating
geometry.
First, the cell is treated with a harmless fluorescent dye that selectively
labels the DNA. Then, two counter-propagating, near-infrared laser beams
are used to create a standing-wave interference pattern in the cell
and excite fluorescence through a two-photon transition. Next, the researchers
turn up the laser power briefly, thereby bleaching some of the dye and
creating a distinctive signal pattern. As the DNA wiggles around, this
pattern gradually washes out and the fluorescence signal recovers.
"If the DNA wasn't moving, we could bleach a pattern and it would
remain frozen in the interference signal forever," Bardeen said.
"By monitoring the decay of the bleached pattern, we can tell that
the DNA is moving, and we can measure that movement to a precision of
about 20 nanometers."
Preliminary measurements have hinted at the occurrence of subdiffusion
within the cell nucleus, Bardeen said. "The chromatin is wobbling
around, apparently bumping into neighboring molecules and not moving
as far as it should have in the time elapsed."
This indicates that molecular crowding is extremely important at the
nanometer length scale, and suggests a major difference between life
and death, Bardeen said. "When a cell is dead, we don't see any
diffusion occurring. In fact, we don't see any movement in the cell
at all."
Cellular motion is not just a simple mechanical operation, Bardeen said.
"Motion is somehow connected with life itself. It's one of the
things that differentiates a living cell from a lump of DNA."
The researchers described their experimental technique and presented
preliminary data on chromatin movement at the American Chemical Society
meeting, held Aug. 26-30 in Chicago.
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