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LOS ANGELES, Sept. 7 (Xinhuanet) --
Small particles of prion protein are much more efficiently
infectious than large ones, yet there is also a lower size
limit below which infectivity is lost, scientists reported on
Wednesday.
Prions are apparently malformed proteins blamed for deadly brain
diseases, such as the mad cow disease in cattle and
Creutzfeldt-Jakob disease in humans. Prion diseases are also
known as transmissible spongiform encephalopathies (TSEs)
because the prions create holes in the brain, giving it a
sponge-like appearance.
In a latest study, researchers from
US National Institute of Allergy and Infectious Diseases
(NIAID) found the link between the proteins' size and their
infectivity. Their findings appear in theSept. 8 issue of the
journal Nature.
The most infectious prions are
significantly smaller than the large thread-like deposits of
protein molecules readily seen in the diseased brains of
infected individuals.
Scientists have known that
infectious prions range widely in size, but now for the first
time the researchers ranked them according to their infective
efficiency, and their findings have placed new limits on the
size of the smallest prion.
Prions appear to be crystal-like
clusters of protein molecules that can grab normal, dissolved
protein molecules and convert them to a solid, crystal-like
state, said Byron Caughey, senior researcher at NIAID's Rocky
Mountain Laboratory.
"Although large prion particles can
do this, and are infectious, you can infect many more
individuals, or cause much more rapid disease in a single
individual, with an equivalent weight of small prion
particles," said Caughey.
"But our findings also suggest that
if the protein cluster is smaller than a certain minimum size,
it becomes unstable and loses its infectious properties."
Normal protein molecules found in
many animals do not cause harm, but they can become lethal and
destroy the brain when they refold and gather into precisely
ordered clusters.
"As you increase particle size
steadily from single molecules to particles containing
thousands of molecules, there's a sudden jump in infectivity
once you get to the minimum infectious particle size (at least
six molecules per particle)," he explained.
"Soon the most infectious particles
appear (equivalent in weight to 14 to 28 molecules per
particle), followed by larger thread-like particles that are
still infectious, but less so, per unit of protein."
These findings are consistent with
evidences in many other neurological protein aggregation
diseases, that small, misfolded clusters are more damaging
than large clusters.
Thus the treatments designed to
break apart large accumulations of prions in the brain might
do more harm than good by releasing the most infectious prion
particles, resulting in more widespread damage, the
researchers noted.
"Large deposits, or plaques, could
be an attempt by the brainto detoxify the infectivity, to
protect the brain," Caughey said.
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