The method, named L-TEAM (Low-TEmperature AMplification), is the result of more than five years of research and offers several advantages over traditional PCR, the dominant technique used to amplify DNA segments of interest.
With its easy-to-use, 'one-pot' design, L-TEAM avoids the need for heating and cooling steps and specialized equipment usually associated with PCR. That means it is an efficient, inexpensive method that can importantly prevent protein denaturation, thereby opening a new route to real-time analysis of living cells.
In their study published in Organic & Biomolecular Chemistry, the researchers introduced synthetic molecules called locked nucleic acids (LNAs) into the DNA strands, as these molecules are known to help achieve greater stability during hybridization.
The addition of LNA led to an unexpected, but beneficial, outcome. The team observed a reduced level of "leak" amplification, a type of non-specific amplification that has long been an issue in DNA amplification studies as it can lead to an error in disease diagnosis, that is, a false positive.
"We were surprised to discover the novel effect of LNA in overcoming the common leak problem in DNA amplification reactions," says Ken Komiya, assistant professor at Tokyo Tech's School of Computing. "We plan to investigate the mechanisms behind leak amplification in detail and further improve the sensitivity and speed of L-TEAM."
In the near future, the method could be used to detect short nucleic acids such as microRNA for medical diagnostics. In particular, it could facilitate point-of-care testing and early disease detection. MicroRNAs are now increasingly recognized as promising biomarkers for cancer detection and may hold the key to uncovering many other aspects of human health and environmental science.
MEDICA-tradefair.com; Source: Tokyo Institute of Technology