A vertically stacked, polymer, microfluidic point mutation analyzer: rapid high accuracy detection of low-abundance K-ras mutations |
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Authors: | Han Kyudong Lee Tae Yoon Nikitopoulos Dimitris E Soper Steven A Murphy Michael C |
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Affiliation: | aDepartment of Nanobiomedical Science and WCU Research Center, Dankook University, Cheonan 330-714, Republic of Korea;bEmerging Technology R&D Lab, LG Electronics Advanced Research Institute, Seoul 137-724, Republic of Korea;cDepartment of Mechanical Engineering, Louisiana State University, Baton Rouge, LA 70803, USA;dCenter for Bio-Modular Multi-Scale Systems, Louisiana State University, Baton Rouge, LA 70803, USA;eDepartment of Chemistry, Louisiana State University, Baton Rouge, LA 70803, USA |
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Abstract: | Recognition of point mutations in the K-ras gene can be used for the clinical management of several types of cancers. Unfortunately, several assay and hardware concerns must be addressed to allow users not well trained in performing molecular analyses the opportunity to undertake these measurements. To provide for a larger user base for these types of molecular assays, a vertically stacked microfluidic analyzer with a modular architecture and process automation was developed. The analyzer employs a primary polymerase chain reaction (PCR) coupled to an allele-specific ligase detection reaction (LDR). Each functional device, including continuous flow thermal reactors for the PCR and LDR, passive micromixers, and ExoSAP-IT purification, was designed and tested. Individual devices were fabricated in polycarbonate using hot embossing and were assembled using adhesive bonding for system assembly. The system produced LDR products from a DNA sample in approximately 1 h, an 80% reduction in time compared with conventional benchtop instrumentation. Purifying the post-PCR products with the ExoSAP-IT enzyme led to optimized LDR performance, minimizing false-positive signals and producing reliable results. Mutant alleles in genomic DNA were quantified to the level of 0.25 ng of mutant DNA in 50 ng of wild-type DNA for a 25-μl sample, equivalent to DNA from 42 mutant cells. |
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Keywords: | K-ras mutation Ligase detection reaction Microfluidic system |
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