Progress towards single-molecule DNA sequencing: a one color demonstration

被引:42
作者
Werner, JH
Cai, H
Jett, JH
Reha-Krantz, L
Keller, RA
Goodwin, PM
机构
[1] Los Alamos Natl Lab, Biosci Div, Los Alamos, NM 87545 USA
[2] Univ Alberta, Dept Biol Sci, Edmonton, AB T6G 2E9, Canada
基金
加拿大自然科学与工程研究理事会; 美国能源部;
关键词
DNA sequencing; single-molecule detection; fluorescence;
D O I
10.1016/S0168-1656(03)00006-3
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
Single molecules of fluorescently labeled nucleotides were detected during the cleavage of individual DNA fragments by a processive exonuclease. In these experiments, multiple (10-100) strands of DNA with tetramethyl rhodamine labeled dUMP (TMR-dUMP) incorporated into the sequence were anchored in flow upstream of the detection region of an ultra sensitive flow cytometer. A dilute solution of Exonuclease I passed over the microspheres. When an exonuclease attached to a strand, processive digestion of that strand began. The liberated, labeled bases flowed through the detection region and were detected at high efficiency at the single-molecule level by laser-induced fluorescence. The digestion of a single strand of DNA by a single exonuclease was discernable in these experiments. This result demonstrates the feasibility of single-molecule DNA sequencing. In addition, these experiments point to a new and practical means of arriving at a consensus sequence by individually reading out identical sequences on multiple fragments. Published by Elsevier Science B.V.
引用
收藏
页码:1 / 14
页数:14
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