Electrophoretic quantitation of nucleic acids without amplification by single-molecule imaging

被引:44
作者
Anazawa, T
Matsunaga, H
Yeung, ES [1 ]
机构
[1] Iowa State Univ, Ames Lab, US DOE, Ames, IA 50011 USA
[2] Iowa State Univ, Dept Chem, Ames, IA 50011 USA
[3] Hitachi Ltd, Cent Res Lab, Kokubunji, Tokyo 1858601, Japan
关键词
D O I
10.1021/ac025801u
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
We have developed a novel high-performance quantitative assay for unamplified nucleic acids that is based on single-molecule imaging. The apparatus is a simple but highly sensitive single-molecule detection system that uses a normal CCD camera instead of an image-intensified CCD camera. After the DNA molecules in a sample were labeled with YOYO-1, they were induced to migrate electrophoretically in a polymer solution and imaged. No chemical or biochemical amplification was required. Direct quantitation of the sample by counting molecules was possible, because the number counted over the measurement period was directly proportional to the concentration of DNA molecules in the sample. Nonspecifically labeled impurities that would degrade the sensitivity of the assay were successfully reduced and discriminated from the DNA molecules by differences in electrophoretic mobility. By using beta-actin DNA (838 bp) as a model sample, we demonstrate that this protocol was fast (10-min measurement period), highly sensitive (limit of quantitation: similar to10(3) copies/sample, or 3x10(-16) M), quantitative, and covered a wide linear dynamic range (similar to10(4)). This high-performance assay promises to be a powerful technology for the quantitation of specific varieties of mRNA in the study of gene functions and diseases and in the clinical detection of mutant cells.
引用
收藏
页码:5033 / 5038
页数:6
相关论文
共 32 条