Scientists reveal how cellular protein detects viruses, sparks immune responseFebruary 20th, 2009 - 5:39 pm ICT by ANI
Washington, February 20 (ANI): Scientists at the University of Illinois say that they have found how a cellular protein recognizes an invading virus and alerts the body to the infection.
Taekjip Ha, a physics professor and Howard Hughes Medical Institute investigator, says that the study settles a debate over how the protein, RIG-I (pronounced rig-EYE), is able to distinguish between viral RNA and self (or cellular) RNA.
“RIG-I is the first molecule in the immune response to detect viral RNA,” said Sua Myong, lead author on the study and a professor at the U. of I.’’s Institute for Genomic Biology.
She pointed out that unlike most other proteins known to detect viral infections only in specialized immune cells, RIG-I is active in every cell type in the body.
The RIG-I protein has two major parts: caspase-recruitment domains (CARDs) and an ATPase domain that consumes ATP, the cellular fuel molecule.
Studies conducted in the past have shown that the CARD domains actually inhibit the activity of RIG-I when no virus is present, but are vital to sounding the alarm and triggering an immune response once a certain type of virus has been detected.
Other research projects have shown that RIG-I recognizes an important feature of viral RNAs that is missing from most human RNAs.
This feature, a “triphosphate” tag at a particular end, the “five-prime” (5”) end, of viral RNA, is a viral fingerprint that tells RIG-I that something is amiss. Detection of this tag starts a cascade of reactions that allows RIG-I to broadcast a message to other cellular components, and ultimately to other cells.
They also knew that RIG-I was usually active in the presence of double-stranded RNA, not the single-stranded RNA found in most animal cells.
Previous studies have also shown that the central ATPase domain is key to the function of the molecule. A single mutation in this region shuts down its activity altogether.
“We knew that the CARD domain was responsible for transmitting the antiviral signaling. And we knew how the 5”-triphosphate tag is detected. But a big question remained about the ATPase domain: It was using ATP to do something but what?” Myong said.
With a view to solving that mystery, the research team used a technique called “protein-induced fluorescent enhancement”which makes use of a fluorescent dye that, when attached to a specific region of a molecule such as RNA, glows with more or less intensity depending on its proximity to a protein that is interacting with that molecule.
They found that the RIG-I protein moves back and forth (translocates) selectively on double-stranded RNA, and that this activity is greatly stimulated in the presence of 5”-triphosphate.
According to Ha, by requiring both the 5”-triphosphate and the double-stranded RNA for it to function, the RIG-I protein is able to very accurately detect a viral invader.
He said that most cellular RNAs have their triphosphate tails bobbed, capped or otherwise modified before circulating in the cytosol of the cell.
“So this is one powerful way of distinguishing viral RNA from cellular RNA,” he added.
Myong said that before conducting the current study, researchers did not know if RIG-I sensed both the double-stranded RNA and the 5”-triphosphate separately, or in an integrated manner.
“Our work bridges the gap. We show that it does both in an integrated manner, she said.
The study has been reported in the journal Science. (ANI)
Tags: animal cells, atp, cellular components, cellular fuel, cellular protein, cellular rna, double stranded rna, fingerprint, howard hughes, howard hughes medical, howard hughes medical institute, hughes medical institute, immune cells, immune response, molecule studies, physics professor, rig, rnas, viral infections, viral rna