Construction of a novel peptide nucleic acid piezoelectric gene sensor microarray detection system

被引:22
作者
Chen, M
Liu, MH
Yu, LL
Cai, GR
Chen, QH
Wu, R
Wang, F
Zhang, B
Jiang, TL
Fu, WL [1 ]
机构
[1] Third Mil Med Univ, SW Hosp, Dept Lab Diag, Chongqing 400038, Peoples R China
[2] Third Mil Med Univ, Daping Hosp, Dept Gynecol & Obstet, Chongqing 400042, Peoples R China
[3] Chinese Elect Sci & Tech Grp Co, Res Inst 26, Chongqing 400060, Peoples R China
关键词
peptide nucleic acid; gene sensor; microarray; HBV;
D O I
10.1166/jnn.2005.223
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A novel 2 x 5 clamped style piezoelectric gene sensor microarray has been successfully constructed. Every crystal unit of the fabricated gene sensor can oscillate independently without interfering with each other. The bis-peptide nucleic acid (bis-PNA) probe, which can combine with target DNA or RNA sequences more effectively and specifically than a DNA probe, was designed and immobilized on the surface of the gene sensor microarray to substitute the conventional DNA probe for direct detection of the hepatitis B virus (HBV) genomic DNA. Detection conditions were then explored and optimized. Results showed that PBS buffer of pH 6.8, an ion concentration of 20 mmol/liter, and a probe concentration of 1.5 mu mol/liter were optimal for the detection system. Under such optimized experimental conditions, the specificity of bis-PNA was proved much higher than that of DNA probe. The relationship between quantity of target and decrease of frequency showed a typical saturation curve when concentrations of target HBV DNA varied from 10 pg/liter to 100 mu g/liter, and 10 mu g/liter was the watershed, with a statistic linear regression equation of I gC = -2.7455 + 0.0691 Delta F and the correlating coefficient of 0.9923. Fortunately, this is exactly the most ordinary variant range of the HBV virus concentration in clinical hepatitis samples. So, a good technical platform is successfully constructed and it will be applied to detect HBV quantitatively in clinical samples.
引用
收藏
页码:1266 / 1272
页数:7
相关论文
共 43 条
[1]   Electropolymerization as a versatile route for immobilizing biological species onto surfaces -: Application to DNA biochips [J].
Bidan, G ;
Billon, M ;
Galasso, K ;
Livache, T ;
Mathis, C ;
Roget, A ;
Torres-Rodriguez, LM ;
Vieil, E .
APPLIED BIOCHEMISTRY AND BIOTECHNOLOGY, 2000, 89 (2-3) :183-193
[2]   In vivo nuclear delivery of oligonucleotides via hybridizing bifunctional peptides [J].
Brandén, LJ ;
Christensson, B ;
Smith, CIE .
GENE THERAPY, 2001, 8 (01) :84-87
[3]   Affinity capture and recovery of DNA at femtomolar concentrations with peptide nucleic acid probes [J].
Chandler, DP ;
Stults, JR ;
Anderson, KK ;
Cebula, S ;
Schuck, BL ;
Brockman, FJ .
ANALYTICAL BIOCHEMISTRY, 2000, 283 (02) :241-249
[4]   Affinity purification of DNA and RNA from environmental samples with peptide nucleic acid clamps [J].
Chandler, DP ;
Stults, JR ;
Cebula, S ;
Schuck, BL ;
Weaver, DW ;
Anderson, KK ;
Egholm, M ;
Brockman, FJ .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2000, 66 (08) :3438-3445
[5]  
Cutrona G, 2003, CANCER RES, V63, P6144
[6]   Sequence-specific targeting of duplex DNA by peptide nucleic acids via triplex strand invasion [J].
Demidov, VV ;
Frank-Kamenetskii, MD .
METHODS, 2001, 23 (02) :108-122
[7]   Site-directed inhibition of DNA replication by triple helix formation [J].
Diviacco, S ;
Rapozzi, V ;
Xodo, L ;
Hélène, C ;
Quadrifoglio, F ;
Giovannangeli, C .
FASEB JOURNAL, 2001, 15 (14) :2660-2668
[8]   Inhibition of gene expression inside cells by peptide nucleic acids: Effect of mRNA target sequence, mismatched bases, and PNA length [J].
Doyle, DF ;
Braasch, DA ;
Simmons, CG ;
Janowski, BA ;
Corey, DR .
BIOCHEMISTRY, 2001, 40 (01) :53-64
[9]   PNA HYBRIDIZES TO COMPLEMENTARY OLIGONUCLEOTIDES OBEYING THE WATSON-CRICK HYDROGEN-BONDING RULES [J].
EGHOLM, M ;
BUCHARDT, O ;
CHRISTENSEN, L ;
BEHRENS, C ;
FREIER, SM ;
DRIVER, DA ;
BERG, RH ;
KIM, SK ;
NORDEN, B ;
NIELSEN, PE .
NATURE, 1993, 365 (6446) :566-568
[10]   EFFICIENT PH-INDEPENDENT SEQUENCE-SPECIFIC DNA-BINDING BY PSEUDOISOCYTOSINE-CONTAINING BIS-PNA [J].
EGHOLM, M ;
CHRISTENSEN, L ;
DUEHOLM, KL ;
BUCHARDT, O ;
COULL, J ;
NIELSEN, PE .
NUCLEIC ACIDS RESEARCH, 1995, 23 (02) :217-222