Nanopore Analysis of Nucleic Acids Bound to Exonucleases and Polymerases

被引:41
作者
Deamer, David [1 ]
机构
[1] Univ Calif Santa Cruz, Dept Biomol Engn, Santa Cruz, CA 95064 USA
来源
ANNUAL REVIEW OF BIOPHYSICS, VOL 39 | 2010年 / 39卷
关键词
single molecule; DNA sequencing; alpha-hemolysin; Klenow fragment; blocking oligomers; active control; single-molecule electrophoresis; T7 DNA polymerase; DNA; DISCRIMINATION; COMPLEXES; MOLECULES; BINDING; IDENTIFICATION; BASE;
D O I
10.1146/annurev.biophys.093008.131250
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
When a voltage is imposed across a thin membrane containing a nanoscopic pore, the electric field generated within the pore captures linear ionized polymers, such as nucleic acids, that are present in the solution bathing the pore. The nucleic acid molecule transiently blocks ionic current as it is translocated through the pore, and modulations of the current provide information about the structure and dynamic motion of the molecule. Altering the imposed voltage allows movement of the DNA molecule in the pore to be controlled. If a DNA-processing enzyme such as an exonuclease or polymerase is present, the enzyme-DNA complex is also drawn to the pore, and further modulations of the ionic current reflect enzyme function at the single-molecule level on millisecond timescales. The combined enzymatic and voltage control of a DNA molecule in the nanopore can be used to sequence the DNA.
引用
收藏
页码:79 / 90
页数:12
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