Jan. 7, 2005
PROTEIN TRANSFORMATION GIVES NEW TWIST TO MEDICAL RESEARCH
Writer: Kathleen Phillips, (979) 845-2872,ka-phillips@tamu.edu
Contact: Dr. Ry Young, (979) 845-2087,ryland@tamu.edu
Dr. Jim Sacchettini, (979) 862-7636,sacchett@tamu.edu
COLLEGE STATION -- It was a transforming moment. Researchers could
barely believe their eyes.
A molecular blob of a protein reshaped itself into a molecular Pacman
in order to free new viruses from the inside of a bacterial cell.
"It's the sort of thing where your graduate student tells you the
results of an experiment and you say, 'You must have made a mistake,'" said
Dr. Ryland Young, Texas Agricultural Experiment Station biochemist.
But then, a good scientist has to be prepared at any time for the old
rule to be disproved, he added.
And that's what happens today when Science magazine reports on the
protein Lyz found to be capable of turning itself into a completely
different structure – a discovery made by Young's graduate student Min Xu
and a team of researchers.
Understanding Lyz could enable medical researchers to design drugs to
turn off or on proteins at the cellular level, which could lead to
treatment for some of the most difficult to cure diseases such as cancer
and HIV.
Lyz is a lysozyme, a protein that degrades the tough cell wall that
covers bacterial cells. The name lysozyme means break-out enzyme as coined
by Alexander Fleming, who was also the inventor of penicillin.
"Lysozymes are everywhere," Young noted. "They are even in your tears,
where they destroy bacteria that try to enter the eye."
But Lyz is made by a virus growing inside the bacterial cell. The virus
has to destroy the cell wall, or the virus babies would be trapped inside
the dead body of the bacterium. Originally, the group set out to study how
the Lyz protein gets outside the cell to break down the cell wall. They
were looking for a holin, a protein that makes holes in the cell membrane
to let the lysozyme out.
"Using biochemistry and genetics, Min and Doug (Struck, a senior research
scientist) found something completely unexpected," Young said. Lyz was
able to get out of the membrane by presenting a part of the protein as a
signal, or tether attached to the membrane. Once outside, Lyz completely
changes its shape, withdrawing the signal from the membrane and turning
into a jaw-like molecule that almost literally chews up the cell wall,
thus allowing release of its progeny.
"It's like one of those transformer toys that you twist and they become
something quite different from the original in shape and form," noted
Dr. Jim Sacchettini, whose group worked out the detailed molecular structure of
Lyz before and after its shape-shifting. "It's fascinating to know now that
the same protein can exist in vastly different states. It's an academic
exercise from which a lot of other interesting work and developments may
derive."
Also working with Xu, Young, Sacchettini and Struck on the project
were: Dr. Sam Arulandu, a post doctoral researcher, and undergraduate
student Stephanie Swanson, a senior from Houston.
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