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NASA Scientists Gain
Insight Into Deadly Disease
Scientists at NASA's
Marshall Space Flight Center
in Huntsville, AL, have taken an important step in understanding the
molecular structure of a disease that afflicts 200 to 300 million
people and is second only to malaria in cause of death worldwide.
The disease, known as Schistosomiasis, is caused by parasites found
in contaminated water.
"We were able
to determine a three-dimensional atomic structure of an important
enzyme from one of four species of parasites known to cause schistosomiasis,"
explained Dr. Daniel Carter, research director and chief of Marshall's
Biophysics and Advanced Materials Branch of the Space Sciences Laboratory.
"That allowed us to identify critical parts of the enzyme's surface
structure which elicit the immune responses to the disease. This
important step seems to offer the most potential for developing
vaccines that protect people against the entire species of schistosomiasis
parasites, not just one species," said Carter.
Using highly
specialized X-ray equipment and protein crystallization techniques
developed for space-based microgravity research, biophysics researchers
were able to locate key positions of individual atoms in the enzyme,
also a major target for drugs used in the treatment of schistosomiasis,
and build a computer picture or blueprint of the schistosoma enzyme
structure.
The determination
of the enzyme structure offers the possibility of combining such
techniques as the use of disease fighting drugs with the development
of preventative vaccines to form an effective barrier against the
transmission of schistosomiasis.
"Building a
person's immunity is one way to fight schistosomiasis," explained
Carter. "Many people are repeatedly infected with the disease. If
we can break the life cycle of the parasite by vaccinating people
against transmission of the disease, we can make a major step toward
eliminating the threat of schistosomiasis in those parts of the
world where it poses a major health hazard."
The research
has paid dividends in other areas as well, said Carter. "Information
gained in the search for a particular atomic structure often helps
us learn more quickly about other research targets," he said. "For
instance, a three-dimensional crystal structure of a schistosomiasis
enzyme joined with atomic structural components of Human Immunodeficiency
Virus type 1 (HIV-1) has also been resolved. This structural, building-
block approach to HIV research has helped us learn more about the
structure of HIV proteins, which have proven very difficult to crystallize
and thus study more thoroughly," said Carter.
Schistosomiasis
research at Marshall was performed in collaboration with the Institute
of Applied Microbiology in Vienna, Austria, and the Center For Advanced
Research in Biotechnology of the National Institute of Standards
in Washington, DC.
Also known
as bilharzia, schistosomiasis is a disease caused by any of four
parasitic flatworms or flukes. Persons can become infected with
schistosomiasis when they wade or swim in contaminated fresh water
by exposure to skin-penetrating, free-swimming larvae. Schistosomiasis
is known to occur in parts of Brazil, Egypt, sub-Saharan Africa,
southern China, the Philippines and Southeast Asia. There is no
vaccine against the disease.
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