Towards a general procedure for sequencing single DNA molecules

被引:36
作者
Stephan, J
Dörre, K
Brakmann, S
Winkler, T
Wetzel, T
Lapczyna, M
Stuke, M
Angerer, B
Ankenbauer, W
Földes-Papp, Z
Rigler, R
Eigen, M
机构
[1] Max Planck Inst Biophys Chem, Abt Biochem Kinet, D-37077 Gottingen, Germany
[2] EVOTEC Biosyst AG, D-22525 Hamburg, Germany
[3] Max Planck Inst Biophys Chem, Abt Laserchem, D-37077 Gottingen, Germany
[4] Roche Diagnost GMBH, Dept Penzberg, D-82372 Penzberg, Germany
[5] Karolinska Inst, S-17177 Stockholm, Sweden
关键词
single molecule detection; DNA labeling; exonucleolytic degradation; microstructures; de novo DNA sequencing;
D O I
10.1016/S0168-1656(00)00417-X
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
In this paper we report on the latest technical advances towards single molecule sequencing, a useful method currently developed especially for fast and easy de novo sequencing. Different approaches for complete labeling of DNA with fluorescent dyes are described. In addition, the experimental set-up for the sequencing process is shown. We demonstrate the ability to purify the buffer and enzyme solutions. Inorganic buffers were purified down to at least 20 fM of remaining fluorescent impurities. The exonuclease buffer solution could be cleaned down to 0.8 pM whereby its full activity was kept. Finally, we show a selection procedure for beads and present the data of a model experiment, in which immobilized DNA is degraded by an exonuclease within a polymethylmethacrylate (PMMA) microstructure. Furthermore, the mathematical processing of the obtained raw data is described. A first complete experimental cycle is shown, combining all preparatory steps which are necessary for single molecule sequencing in microstructures. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:255 / 267
页数:13
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