Single-molecule dynamics of the Eco RI enzyme using stretched DNA:: its application to in situ sliding assay and optical DNA mapping

被引:21
作者
Kabata, H [1 ]
Okada, W [1 ]
Washizu, M [1 ]
机构
[1] Kyoto Univ, Dept Mech Engn, Micromachine Lab, Sakyo Ku, Kyoto 6068501, Japan
来源
JAPANESE JOURNAL OF APPLIED PHYSICS PART 1-REGULAR PAPERS SHORT NOTES & REVIEW PAPERS | 2000年 / 39卷 / 12B期
关键词
nanomachine; enzyme; DNA; sliding; sequence specificity; dielectrophoresis; visualization; genome mapping; Bio MEMS;
D O I
10.1143/JJAP.39.7164
中图分类号
O59 [应用物理学];
学科分类号
摘要
The Eco RI enzyme is a nanomachine responsible for gene integrity in cells, and has a sensor that discriminates its specific binding sequence on DNA (GAATTC) from flanking nonspecific sequences. We applied this sequence sensing ability to microscopic DNA mapping. Visible measurement of positions of the GAATTC sequence was accomplished with fluorescently labeled Ecc, RI and DNA that was stretched by dielectrophoresis and suspended above a glass surface. Statistics showed that Eco RI molecules were trapped at particular positions on stretched DNA where GAATTC sequences are located. Dwell time at trapped positions agreed with the lifetime of the specific DNA-Eco RI complex previously measured. In a flowing stream, Eca RI molecules moved along stretched DNA and were trapped at putative GAATTC sequences, providing evidence of sliding as a mechanism for relocation of Eco RI on DNA. This single-molecule-based method can he a lab on a chip for mapping genomic DNA and analyzing motility of DNA-binding nanomachines.
引用
收藏
页码:7164 / 7171
页数:8
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