CHAPEL HILL - Chemists working at the University of North Carolina at Chapel Hill have developed a simple new way of detecting tiny genetic mutations responsible for medical conditions including cystic fibrosis and cancer.
Those alternations, called single nucleotide polymorphisms, occur when one chemical component of the genetic code is changed in some way by additions, deletions or relocations of genetic material, the scientists say. Knowing what and where those changes are is critical to finding and designing drugs that can act on them specifically without interfering with the activity of healthy genes.
Potentially, the new method could allow scientists to screen for minute changes in the genetic makeup of humans, animals, plants or viruses, UNC-CH's Dr. Holden Thorp said. Comparable techniques already available for screening genes are confined to research laboratories, are labor intensive and are therefore slow and expensive.
Dr. Patricia A Ropp, postdoctoral research associate in pharmacology at the UNC-CH School of Medicine, and Thorp, professor of chemistry, have been developing the new method. In a paper published in the September issue of the journal Chemistry and Biology, the two describe it.
"Our method uses inexpensive electronic equipment without cumbersome procedures," Thorp said. "It is based on the measurement of different but very small electrical currents generated when guanine is paired with its correct DNA chemical partner versus an incorrect chemical partner."
The incorrect chemical is a single nucleotide polymorphism mutation or SNP, he said. With the new technique, he and Ropp can detect specific mutations associated with specific diseases.
"As we can continue to make these kinds of advances, we'll eventually have a device that can be used to do these analyses routinely so that they will impact people's everyday lives," Thorp said. "It's very exciting."