An Instrument for Automated Purification of Nucleic Acids from Contaminated Forensic Samples
Forensic crime scene sample analysis, by its nature, often deals with samples in which there are low amounts of nucleic acids, on substrates that often lead to inhibition of subsequent enzymatic reactions such as PCR amplification for Short Tandem Repeat (STR) profiling. Common substrates include denim from blue jeans, which yields indigo dye as a PCR inhibitor, and soil, which yields humic substances as inhibitors. These inhibitors frequently co-extract with nucleic acids in standard column or bead-based preps, leading to frequent failure of STR profiling. We present a novel instrument for DNA purification of forensic samples that is capable of highly effective concentration of nucleic acids from soil particulates, fabric, and other complex samples including solid components. The novel concentration process, known as Synchronous Coefficient of Drag Alteration, is inherently selective for long-charged polymers such as DNA, and therefore is able to effectively reject known contaminants. We present an automated sample preparation instrument based on this process, and preliminary results based on mock forensic samples.
1University of British Columbia, Vancouver, British Columbia, Canada
2Royal Canadian Mounted Police Forensic Laboratory Services, Vancouver, British Columbia, Canada
Correspondence: Andre Marziali, Ph.D., University of British Columbia, Department of Physics and Astronomy, 6224 Agricultural Road, Vancouver, BC, Canada V6T 1Z1; Phone: +1.604.822.4514; Fax: +1.604.822.4202
∗∗ Authors contributed equally to this publication.