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

被引:114
作者
Dimov, Ivan K. [1 ,3 ]
Garcia-Cordero, Jose L. [1 ]
O'Grady, Justin [2 ]
Poulsen, Claus R. [1 ]
Viguier, Caroline [1 ]
Kent, Lorcan [1 ]
Daly, Paul [1 ]
Lincoln, Bryan [1 ]
Maher, Majella [2 ]
O'Kennedy, Richard [1 ]
Smith, Terry J. [2 ]
Ricco, Antonio J. [1 ]
Lee, Luke P. [1 ,4 ]
机构
[1] Dublin City Univ, Natl Ctr Sensor Res, Biomed Diagnost Inst, Dublin 9, Ireland
[2] Natl Univ Ireland Univ Coll Galway, Biomed Diagnost Inst, Galway, Ireland
[3] Univ Valparaiso, Dept Biomed Engn, Valparaiso, Chile
[4] Univ Calif Berkeley, Berkeley Sensor & Actuator Ctr, Dept Bioengn, Biomol Nanotechnol Ctr, Berkeley, CA 94720 USA
关键词
D O I
10.1039/b812515e
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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 mu L of crude lysate in under 30 min for the entire process.
引用
收藏
页码:2071 / 2078
页数:8
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