Researchers at National Jewish Medical and Research Center have developed a method for finding the molecular targets of the immune system, known as antigens. The method extends a widely used technique, called library display, to more complex proteins. It could have broad applications in biological and medical research. The research team, led by National Jewish and Howard Hughes Medical Institute immunologist John W. Kappler, Ph.D., is already collaborating with teams looking for causes of the autoimmune disease rheumatoid arthritis, developing cancer vaccines, and understanding the molecular triggers of chronic beryllium disease. The technique is described in the April 2004 issue of PloS Biology (www.plosbiology.org
), a publication of the Public Library of Science.
"Our technique allows us to fish in a vast library of protein fragments for the specific ones that bind to T cells and trigger an immune-system attack," said Dr. Kappler. "We believe that researchers using this technique will extend its usefulness beyond T-cells and antigens to interactions involving a wide variety of biologically important proteins."
T cells are the sentinels of the immune system. Millions of T cells circulate in the body looking for infectious organisms or other foreign invaders. Each T cell carries a receptor that can recognize a specific protein fragment. Cells known as antigen-presenting cells display on their surfaces these protein fragments bound to a molecule known as MHC. When a specific T cell encounters a protein-MHC complex its receptor can bind, it becomes activated. That sets off a cascade of events that tells the immune system to attack that protein fragment and the organism it comes from.
In most cases it is very difficult for scientists to determine what protein-MHC complex a particular T-cell receptor binds, and thus where the immune system is aiming its attack. Dr. Kappler, who was one of the original discoverers oPage: 1 2 Related biology news :1
Contact: William Allstetter
National Jewish Medical and Research Center
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