Integrated microfluidic tmRNA purification and real-time NASBA device for molecular diagnostics

Ivan K. Dimov(University of Valparaíso), José L. García-Cordero(Dublin City University), Justin O’Grady(Ollscoil na Gaillimhe – University of Galway), Claus Poulsen(Dublin City University), Caroline Viguier(Dublin City University), Lorcan Kent(Dublin City University), Paul Daly(Dublin City University), Bryan Lincoln(Dublin City University), Majella Maher(Ollscoil na Gaillimhe – University of Galway), Richard O’Kennedy(Dublin City University), Terry Smith(Ollscoil na Gaillimhe – University of Galway), Antonio J. Ricco(Dublin City University), Luke P. Lee(University of California, Berkeley)
Lab on a Chip
January 1, 2008
Cited by 142Open Access
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Abstract

We demonstrate the first integrated microfluidic tmRNA purification and nucleic acid sequence-based amplification (NASBA) device incorporating real-time detection. The real-time amplification and detection step produces pathogen-specific response in < 3 min from the chip-purified RNA from 100 lysed bacteria. On-chip RNA purification uses a new silica bead immobilization method. On-chip amplification uses custom-designed high-selectivity primers and real-time detection uses molecular beacon fluorescent probe technology; both are integrated on-chip with NASBA. Present in all bacteria, tmRNA (10Sa RNA) includes organism-specific identification sequences, exhibits unusually high stability relative to mRNA, and has high copy number per organism; the latter two factors improve the limit of detection, accelerate time-to-positive response, and suit this approach ideally to the detection of small numbers of bacteria. Device efficacy was demonstrated by integrated on-chip purification, amplification, and real-time detection of 100 E. coli bacteria in 100 microL of crude lysate in under 30 min for the entire process.


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