Forensic DNA testing is extensively used to link individuals to crimes, establish paternity, solve missing person cases, identify casualties in military and mass fatality events, and provide genealogical histories. Typically, it takes a skilled technician in a properly equipped laboratory 1-2 days to extract DNA from a sample, quantify the amount, make multiple copies of specific genetic sequences (PCR amplification), and then create a "DNA signature" that is unique to an individual. However, when crude samples are the source of the desired DNA, the contaminants and particulates mixed in with the genetic material can seriously complicate the reading of a complete and accurate DNA signature. The additional purification steps needed for conventional means of handling crude samples, such as filtering, not only lengthen the processing time but also tend to reduce the quantity and concentration of DNA delivered—making human identification more difficult or impossible.
The new NIST/ARA technique is based on one the team first developed four years ago** for crude samples called "gradient elution moving boundary electrophoreses" or GEMBE. GEMBE separates specific components of a sample by a molecular "tug-of-war." The sample is pushed in one direction by an electric field and in the other by the counterflow of a buffer solution. Gradually reducing the buffer flow allows selected components from the sample to pass into a microfluidic channel to be analyzed. Unwanted components of the crude sample are kept out. (For details, see "'No Muss, No Fuss' Miniaturized Analysis for Complex Samples Developed" in NIST Tech Beat, Nov. 17, 2009, and "Researchers Expand Capabilities of Miniature Analysis for Complex Samples" in NIST Tech Beat, Aug. 30, 2011.)
To work with DNA, the researchers modified GEMBE so that two different buffer solutions—one with ions that move quickly and one with ions that move slowly during electrophoresis—are placed in the separate reservoirs connected by the microchannel. When a crude sample is suspended in the slow ion solution and electric current is applied, the DNA within the sample moves into the microchannel and concentrates at the interface between the two buffers. Unwanted contaminants and particulates—including those that can inhibit PCR amplification—are left behind. The collected DNA can be quantified directly in the microchannel and then delivered into a vial for further processing.
To demonstrate the forensic capabilities of its new technique, the NIST/ARA team extracted, purified, quantified and concentrated human genomic DNA from both clean and dirty buccal (cheek cell) swabs. In both cases, the process yielded full DNA signatures.
*E.A. Strychalski, C. Konek, E.L.R. Butts, P.M. Vallone, A.C. Henry and D. Ross. DNA purification from crude samples for human identification using gradient elution isotachophoresis. Electrophoresis, Vol. 34, No.17, pp. 2522–2530. Published online Sept. 2, 2013. DOI 10.1002/elps.201300133.
**www.nist.gov/public_affairs/tech-beat/tb20091117.cfm#gembe and www.nist.gov/public_affairs/tech-beat/tb20110830.cfm#gembeSource: