A microfluidic biosensor based on nucleic acid sequence recognition

被引:71
作者
Kwakye, S [1 ]
Baeumner, A [1 ]
机构
[1] Cornell Univ, Dept Biol & Environm Engn, Ithaca, NY 14853 USA
基金
美国国家科学基金会;
关键词
biosensor; microfluidics; rapid detection; probe hybridization; microfabrication; liposomes;
D O I
10.1007/s00216-003-2063-2
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The development of a generic semi-disposable microfluidic biosensor for the highly sensitive detection of pathogens via their nucleic acid sequences is presented in this paper. Disposable microchannels with defined areas for capture and detection of target pathogen RNA sequence were created in polydimethylsiloxane (PDMS) and mounted onto a reusable polymethylmethacrylate (PMMA) stand. Two different DNA probes complementary to unique sequences on the target pathogen RNA serve as the biorecognition elements. For signal generation and amplification, one probe is coupled to dye encapsulated liposomes while the second probe is coupled to superparamagnetic beads for target immobilization. The probes hybridize to target RNA and the liposome-target-bead complex is subsequently captured on a magnet. The amount of liposomes captured correlates directly to the concentration of target sequence and is quantified using a fluorescence microscope. Dengue fever virus serotype 3 sequences and probes were used as a model analyte system to test the sensor. Probe binding and target capture conditions were optimized for sensitivity resulting in a detection limit of as little as 10 amol muL(-1) (10 pmol L-1). Future biosensors will be designed to incorporate a mixer and substitute the, fluorescence detection with an electrochemical detection technique to provide a truly portable microbiosensor system.
引用
收藏
页码:1062 / 1068
页数:7
相关论文
共 23 条
[11]  
JINGDONG X, 2000, ANAL CHEM, V72, P1930
[12]   DETECTION OF DENGUE VIRUS BY INSITU HYBRIDIZATION [J].
KILLEN, H ;
OSULLIVAN, MA .
JOURNAL OF VIROLOGICAL METHODS, 1993, 41 (02) :135-146
[13]   Chemical amplification: Continuous-flow PCR on a chip [J].
Kopp, MU ;
de Mello, AJ ;
Manz, A .
SCIENCE, 1998, 280 (5366) :1046-1048
[14]   Detection of dengue viruses in field caught male Aedes aegypti and Aedes albopictus (Diptera: Culicidae) in Singapore by type-specific PCR [J].
Kow, CY ;
Koon, LL ;
Yin, PF .
JOURNAL OF MEDICAL ENTOMOLOGY, 2001, 38 (04) :475-479
[15]   Detection of dengue virus RNA in patients after primary or secondary dengue infection by using the TaqMan automated amplification system [J].
Laue, T ;
Emmerich, P ;
Schmitz, H .
JOURNAL OF CLINICAL MICROBIOLOGY, 1999, 37 (08) :2543-2547
[16]   Comparison of liposome amplification and fluorophor detection in flow-injection immunoanalyses [J].
Lee, MY ;
Durst, RA ;
Wong, RB .
ANALYTICA CHIMICA ACTA, 1997, 354 (1-3) :23-28
[17]   PLANAR CHIPS TECHNOLOGY FOR MINIATURIZATION AND INTEGRATION OF SEPARATION TECHNIQUES INTO MONITORING SYSTEMS - CAPILLARY ELECTROPHORESIS ON A CHIP [J].
MANZ, A ;
HARRISON, DJ ;
VERPOORTE, EMJ ;
FETTINGER, JC ;
PAULUS, A ;
LUDI, H ;
WIDMER, HM .
JOURNAL OF CHROMATOGRAPHY, 1992, 593 (1-2) :253-258
[18]   Fabrication of plastic microfluid channels by imprinting methods [J].
Martynova, L ;
Locascio, LE ;
Gaitan, M ;
Kramer, GW ;
Christensen, RG ;
MacCrehan, WA .
ANALYTICAL CHEMISTRY, 1997, 69 (23) :4783-4789
[19]  
MONDESIRE R, 2000, IVD MAGAZINE MAY, P9
[20]   DNA chips: State-of-the-art [J].
Ramsay, G .
NATURE BIOTECHNOLOGY, 1998, 16 (01) :40-44