Quantitative PCR based expression analysis on a nanoliter scale using polymer nano-well chips

被引:27
作者
Dahl, Andreas
Sultan, Marc
Jung, Alexander
Schwartz, Regine
Lange, Matthias
Steinwand, Michael
Livak, Kenneth J.
Lehrach, Hans
Nyarsik, Lajos
机构
[1] Max Planck Inst Mol Genet, Dept Vertebrate Genom, D-14195 Berlin, Germany
[2] Appl Biosyst PE Deutschland GmbH, D-88662 Uberlingen, Germany
[3] Free Univ Berlin, Fachbereich Biol, D-14195 Berlin, Germany
关键词
qPCR; miniaturization; expression analysis; real-time detection; high density microtiterplates; ENZYMATIC AMPLIFICATION; MICROCHAMBER ARRAY; DNA AMPLIFICATION; KINETIC PCR;
D O I
10.1007/s10544-006-9034-2
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The analysis of gene expression is an essential element of functional genomics. Expression analysis is mainly based on DNA microarrays due to highly parallel readout and high throughput. Quantitative PCR (qPCR) based expression profiling is the gold standard for the precise monitoring of selected genes, and therefore used for validation of microarray data. Doing qPCR-based expression analysis in an array-like format can combine the higher sensitivity and accuracy of the qPCR methodology with a high data density at relatively low costs. This paper describes the development of an open-well based miniaturized platform for liquid PCR-based assays on the nanoliter scale using cost-effective polypropylene micro reactors (mu PCR Chip). We show the quantification ability and reliability of qPCR in 200 nl with the mu PCR chip down to 5 starting target molecules using TaqMan (R) chemistry. An RNA expression analysis of four genes in mouse brain, liver and kidney tissues showed similar results in 200 nl as compared to standard 10 mu l assays. The high sensitivity and quantification capability of the mu PCR chip platform developed herein makes it a promising technology for performing high-throughput qPCR-based analysis in the nanoliter volume range.
引用
收藏
页码:307 / 314
页数:8
相关论文
共 27 条
[1]   Quantitative RT-PCR: Pitfalls and potential [J].
Freeman, WM ;
Walker, SJ ;
Vrana, KE .
BIOTECHNIQUES, 1999, 26 (01) :112-+
[2]  
Gitton Y, 2002, NATURE, V420, P586, DOI 10.1038/nature01178
[3]   Real-time nucleic acid sequence-based amplification in nanoliter volumes [J].
Gulliksen, A ;
Solli, L ;
Karlsen, F ;
Rogne, H ;
Hovig, E ;
Nordstrom, T ;
Sirevåg, R .
ANALYTICAL CHEMISTRY, 2004, 76 (01) :9-14
[4]   KINETIC PCR ANALYSIS - REAL-TIME MONITORING OF DNA AMPLIFICATION REACTIONS [J].
HIGUCHI, R ;
FOCKLER, C ;
DOLLINGER, G ;
WATSON, R .
BIO-TECHNOLOGY, 1993, 11 (09) :1026-1030
[5]   Nanoliter scale PCR with TaqMan detection [J].
Kalinina, O ;
Lebedeva, I ;
Brown, J ;
Silver, J .
NUCLEIC ACIDS RESEARCH, 1997, 25 (10) :1999-2004
[6]   Fabrication of plastic microchips by hot embossing [J].
Kricka, LJ ;
Fortina, P ;
Panaro, NJ ;
Wilding, P ;
Alonso-Amigo, G ;
Becker, H .
LAB ON A CHIP, 2002, 2 (01) :1-4
[7]   Single-molecule DNA amplification and analysis in an integrated microfluidic device [J].
Lagally, ET ;
Medintz, I ;
Mathies, RA .
ANALYTICAL CHEMISTRY, 2001, 73 (03) :565-570
[8]   Array of hope [J].
Lander, ES .
NATURE GENETICS, 1999, 21 (Suppl 1) :3-4
[9]   A massively parallel PicoTiterPlate™ based platform for discrete picoliter-scale polymerase chain reactions [J].
Leamon, JH ;
Lee, WL ;
Tartaro, KR ;
Lanza, JR ;
Sarkis, GJ ;
deWinter, AD ;
Berka, J ;
Lohman, KL .
ELECTROPHORESIS, 2003, 24 (21) :3769-3777
[10]   ALLELIC DISCRIMINATION BY NICK-TRANSLATION PCR WITH FLUOROGENIC PROBES [J].
LEE, LG ;
CONNELL, CR ;
BLOCH, W .
NUCLEIC ACIDS RESEARCH, 1993, 21 (16) :3761-3766