WATCHING INDIVIDUAL PROTEINS ACTING ON SINGLE MOLECULES OF DNA

被引:31
作者
Amitani, Ichiro [1 ,2 ]
Liu, Bian [1 ,2 ,3 ]
Dombrowski, Christopher C. [1 ,2 ]
Baskin, Ronald J. [2 ]
Kowalczykowski, Stephen C. [1 ,2 ,3 ]
机构
[1] Univ Calif Davis, Dept Microbiol, Davis, CA 95616 USA
[2] Univ Calif Davis, Dept Mol & Cellular Biol, Davis, CA 95616 USA
[3] Univ Calif Davis, Biophys Grad Grp, Davis, CA 95616 USA
来源
METHODS IN ENZYMOLOGY, VOL 472: SINGLE MOLECULE TOOLS, PT A: FLUORESCENCE BASED APPROACHES | 2010年 / 472卷
关键词
RAD51 NUCLEOPROTEIN FILAMENT; RECOMBINATION HOTSPOT-CHI; ESCHERICHIA-COLI RECA; DOUBLE-STRANDED DNA; RECBCD ENZYME; SACCHAROMYCES-CEREVISIAE; PROCESSIVE TRANSLOCATION; YEAST RAD51; DUPLEX DNA; EXCHANGE;
D O I
10.1016/S0076-6879(10)72007-3
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In traditional biochemical experiments, the behavior of individual proteins is obscured by ensemble averaging. To better understand the behavior of proteins that bind to and/or translocate on DNA, we have developed instrumentation that uses optical trapping, microfluidic solution delivery, and fluorescent microscopy to visualize either individual proteins or assemblies of proteins acting on single molecules of DNA. The general experimental design involves attaching a single DNA molecule to a polystyrene microsphere that is then used as a microscopic handle to manipulate individual DNA molecules with a laser trap. Visualization is achieved by fluorescently labeling either the DNA or the protein of interest, followed by direct imaging using high-sensitivity fluorescence microscopy. We describe the sample preparation and instrumentation used to visualize the interaction of individual proteins with single molecules of DNA. As examples, we describe the application of these methods to the study of proteins involved in recombination-mediated DNA repair, a process essential for the maintenance of genomic integrity.
引用
收藏
页码:261 / 291
页数:31
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