纳斯巴
溶解
核酸
核糖核酸
细菌
检出限
分子信标
微流控
生物
化学
分子生物学
色谱法
DNA
寡核苷酸
纳米技术
基因
生物化学
材料科学
遗传学
作者
Ivan K. Dimov,José L. García-Cordero,Justin O’Grady,Claus Poulsen,Caroline Viguier,Lorcan Kent,Paul Daly,Bryan Lincoln,Majella Maher,Richard O’Kennedy,Terry Smith,Antonio J. Ricco,Luke P. Lee
出处
期刊:Lab on a Chip
[Royal Society of Chemistry]
日期:2008-01-01
卷期号:8 (12): 2071-2071
被引量:142
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 microL of crude lysate in under 30 min for the entire process.
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