RNA expression profiling at the single molecule level

被引:54
作者
Hesse, Jan
Jacak, Jaroslaw
Kasper, Maria
Regl, Gerhard
Eichberger, Thomas
Winklmayr, Martina
Aberger, Fritz
Sonnleitner, Max
Schlapak, Robert
Howorka, Stefan
Muresan, Leila
Frischauf, Anna-Maria [1 ]
Schuetz, Gerhard J.
机构
[1] Johannes Kepler Univ Linz, Inst Biophys, A-4040 Linz, Austria
[2] Salzburg Univ, Dept Mol Biol, Div Genom, A-5020 Salzburg, Austria
[3] Upper Austrian Res GmbH, Ctr Biomed Nanotechnol, A-4020 Linz, Austria
[4] Johannes Kepler Univ Linz, Dept Knowledge Based Math Syst, A-4040 Linz, Austria
基金
奥地利科学基金会;
关键词
D O I
10.1101/gr.4999906
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We developed a microarray platform for PCR amplification-independent expression profiling of minute samples. A novel scanning system combined with specialized biochips enables detection down to individual fluorescent oligonucleotide molecules specifically hybridized to their complementary sequence over the entire biochip surface of cm(2) size. A detection limit of 1.3 fM target oligonucleotide concentration - corresponding to only 39,000 molecules in the sample solution - and a dynamic range of 4.7 orders of magnitude have been achieved. The applicability of the system to PCR amplification-independent gene-expression profiling of minute samples was demonstrated by complex hybridization of cDNA derived from the equivalent of only 104 cells, which matches results obtained in ensemble studies on large samples. By counting each hybridized molecule on the microarray, the method is insusceptible to gene-specific variations of the labeling, thereby representing a principle advance to conventional ensemble-based microarray analysis.
引用
收藏
页码:1041 / 1045
页数:5
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