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Ancient Enzymes Function Like Nanopistons To Unwind RNA
Molecular biologists at The University of Texas at Austin have solved one of the mysteries of how double-stranded RNA is remodeled inside cells in both their normal and disease states. The discovery may have implications for treating cancer and viruses in humans.
They use chemical energy to clamp down and pry open RNA strands, thereby enabling the formation of new structures. This remodeling of RNA is essential to the basic functioning of cells.
In all cellular organisms RNA (ribonucleic acid) plays a fundamental role in the translation of genetic information into the synthesis of proteins. DEAD-box proteins are the largest family of what are known as RNA helicases, which unwind RNA.
Credit: Wikipedia
“It has been known for some time that these enzymes do not function like traditional helicases,” saidEckhard Jankowsky, professor of biochemistry at Case Western Reserve University Medical School. “The research by Lambowitz and his colleagues now provides the critical information that explains how the unwinding reaction works. It marks a major step toward understanding the molecular mechanics for many steps in RNA biology.”
Lambowitz said that the basic insight came when Anna Mallam, a postdoctoral researcher in his lab, hypothesized that DEAD-box proteins function modularly. One area on the protein binds to an ATP molecule, which is the energy source. Another area binds to the double-stranded RNA.
“Once the second domain is latched on to the RNA,” said Mallam, “and the first has got its ATP, the ‘piston’ comes down. It has a sharp edge that drives between the two strands and also grabs on one strand and bends it out of the way.”
Lambowitz, Mallam and their colleagues uncovered this mechanism in Mss116p, a DEAD-box protein in yeast. The mechanism is almost certainly universal to the entire family of the proteins, however, and therefore to all domains of life.
“Every DEAD-box protein that we know about has the same structure,” said Lambowitz, “and they all presumably use the same mechanism.”
This flexibility of DEAD-box proteins is essential to the functioning of healthy cells, which rely on a range of RNA molecules for basic processes, including protein synthesis.
This flexibility is also hijacked in cancers — where over-expression of DEAD-box proteins may help drive uncontrolled cell proliferation — and in infections caused by bacteria, fungi and viruses, which rely on specific DEAD-box proteins for their propagation.
“These findings could have far-reaching implications for our ability to control the activities of proteins in this class when their functions go awry in disease states,” said Michael Bender, program director in the Division of Genetics and Developmental Biology at the National Institutes of Health, which partially funded the work.
Lambowitz even sees potential, much further down the line, for using the nanopistons as the basis of biomedical technology.
“You can even envision, in the far future, how they might be incorporated into artificial nanomachines,” he said, “for switches and other mechanical devices inside and outside the cell.”
