Islamabad, Jan 14 :
When most people in the developed world think of measles, what comes to mind is
only a dim memory of a vaccination at a pediatrician's office. But while
childhood vaccination has virtually eliminated measles from North America and
much of Europe, researchers remain interested in the virus.
This
fascination persists partly because improving the measles vaccine could help
eliminate the more than 10 million measles infections and 150,000 measles-caused
deaths that still occur worldwide. But it also has another source: Scientists
believe that modified measles viruses can be "re-targeted" to attack only tumor
cells, and thus transformed into a powerful new therapy for cancer.
Now,
a new discovery about the process by which measles invades cells has brought the
dream of transforming the virus into a weapon against cancer one step closer to
reality. A research team including scientists from the University of Texas
Medical Branch at Galveston and the Mayo Clinic in Rochester, Minn. have
produced a detailed picture of the intricate molecular mechanism that measles
virus uses to attach to and enter the cells it infects.
The key players
are two proteins that form the spherical envelope surrounding the genetic
material of the measles virus. One is an attachment protein that binds to
receptor molecules on the outer membrane of a host cell, and the other is a
fusion protein that merges the viral envelope with the cell membrane, enabling
the virus to infect the cell. The study, published in the recent issue of Nature
Structural Biology & Molecular Biology demonstrated that the intrinsic
flexibility of the attachment protein is a necessary condition to initiate the
cell fusion process.
"The overall goal of our Mayo Clinic collaborator,
Roberto Cattaneo, is to redirect the measles virus to attack specific cancer
cells, and to accomplish that he and his group need to know as much as they can
about the mechanisms of measles infection," said UTMB professor Werner Braun, an
author of the study. "We have a long-standing collaboration with his group,
using our theoretical predictions and computational methods to help them better
target their experimental work."
UTMB Health research scientist Numan
Oezguen used computer-based molecular modeling to predict interaction sites and
suggested specific mutations that would alter the interaction and mobility of
the attachment protein heads. Results of these experiments performed by the Mayo
Clinic team -- led by Cattaneo -- showed that cell entry of the measles virus
depends on a twisting motion of the attachment protein's heads.
To
produce an accurate portrait of the dynamic mechanism the Mayo Clinic group
created measles viruses with mutations affecting the mobility of their
attachment protein heads, and then tested the mutated viruses to determine each
type's ability to infect cells. "What Dr. Cattaneo's experiments showed was that
the motion of these two parts of the attachment protein has a dramatic effect on
infectivity," Braun said. "In a simplified sense, we think this works like a
lever -- if the cell receptors pull on the attachment protein properly, they
generate this type of motion, and this triggers the fusion protein and leads to
infectivity."
Other authors of the paper include Cattaneo, Chanakha
Navaratnarajah, Levi Rupp, Leah Kay and Vincent Leonard of the Mayo Clinic. The
National Institutes of Health and the Mayo Clinic Cancer Center supported this
research.
Ends
SA/EN
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