Highly sensitive amplified electronic detection of DNA by biocatalyzed precipitation of an insoluble product onto electrodes

被引:74
作者
Patolsky, F [1 ]
Lichtenstein, A [1 ]
Willner, I [1 ]
机构
[1] Hebrew Univ Jerusalem, Inst Chem, IL-91904 Jerusalem, Israel
关键词
bioelectronics; biosensors; DNA; gene technology; monolayers;
D O I
10.1002/chem.200390131
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The amplified detection of a target DNA, based on the alkaline phosphatase oxidative hydrolysis of the soluble 5-bromo-4-chloro-3-indoyl phosphate to the insoluble indigo product as an amplification path, is addressed by two different sensing configurations. The accumulation of the insoluble product on Au electrodes or Au/quartz crystals alters the interfacial electron-transfer resistance at the Au electrode or the mass associated with the piezoelectric crystal, thus enabling the quantitative transduction of the DNA sensing by Faradaic impedance spectroscopy or microgravimetric quartz crystal microbalance measurements, respectively. One sensing configuration involves the association of a complex consisting of the target DNA and a biotinylated oligonucleotide to the functionalized transducers. The binding of the avidin/alkaline phosphatase conjugate to the sensing interface followed by the biocatalyzed precipitation provides the amplification path for the analysis of the target DNA. This analysis scheme was used to sense the target DNA with a sensitivity limit that corresponds to 5 x 10(-14) M. ne second amplified detection scheme involves the use of a nucleic-acid-functionalized alkaline phosphatase as a biocatalytic conjugate for the precipitation of the insoluble product. Following this scheme, the functionalized transducers are interacted with the analyzed sample that was pretreated with the oligonucleotide-modified alkaline phosphatase, followed by the biocatalyzed precipitation as the amplification route for the analysis of the target DNA. By the use of this configuration, a detection limit corresponding to 5 x 10(-13) M was achieved. Real clinical samples of the Tay-Sachs genetic disorder were easily analyzed by the developed detection routes.
引用
收藏
页码:1137 / 1145
页数:9
相关论文
共 47 条
[1]   A quartz crystal microbalance assay for detection of antibodies against the recombinant African swine fever virus attachment protein p12 in swine serum [J].
Abad, JM ;
Pariente, F ;
Hernández, L ;
Lorenzo, E .
ANALYTICA CHIMICA ACTA, 1998, 368 (03) :183-189
[2]   Analysis of biosensor chips for identification of nucleic acids [J].
Arlinghaus, HF ;
Kwoka, MN ;
Jacobson, KB .
ANALYTICAL CHEMISTRY, 1997, 69 (18) :3747-3753
[3]  
BARD AJ, 1980, ELECTROCHEMICAL METH
[4]   Sensing and amplification of oligonucleotide-DNA interactions by means of impedance spectroscopy: a route to a Tay-Sachs sensor [J].
Bardea, A ;
Patolsky, F ;
Dagan, A ;
Willner, I .
CHEMICAL COMMUNICATIONS, 1999, (01) :21-22
[5]   Amplified microgravimetric quartz crystal-microbalance analyses of oligonucleotide complexes: a route to a Tay-Sachs biosensor device [J].
Bardea, A ;
Dagan, A ;
Ben-Dov, I ;
Amit, B ;
Willner, I .
CHEMICAL COMMUNICATIONS, 1998, (07) :839-840
[6]  
Barton J. K., 2004, ANGEW CHEM INT EDIT, V36, P2714
[7]   Mutation detection by electrocatalysis at DNA-modified electrodes [J].
Boon, EM ;
Ceres, DM ;
Drummond, TG ;
Hill, MG ;
Barton, JK .
NATURE BIOTECHNOLOGY, 2000, 18 (10) :1096-1100
[8]   Enzyme-amplified amperometric detection of hybridization and of a single base pair mutation in an 18-base oligonucleotide on a 7-μm-diameter microelectrode [J].
Caruana, DJ ;
Heller, A .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1999, 121 (04) :769-774
[9]   Direct enzyme-amplified electrical recognition of a 30-base model oligonucleotide [J].
deLumleyWoodyear, T ;
Campbell, CN ;
Heller, A .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1996, 118 (23) :5504-5505
[10]   IMPEDANCE BASED SENSING OF THE SPECIFIC BINDING REACTION BETWEEN STAPHYLOCOCCUS ENTEROTOXIN-B AND ITS ANTIBODY ON AN ULTRA-THIN PLATINUM FILM [J].
DESILVA, MS ;
ZHANG, Y ;
HESKETH, PJ ;
MACLAY, GJ ;
GENDEL, SM ;
STETTER, JR .
BIOSENSORS & BIOELECTRONICS, 1995, 10 (08) :675-682