TY - CHAP
T1 - Watching Individual Proteins Acting on Single Molecules of DNA
AU - Amitani, Ichiro
AU - Liu, Bian
AU - Dombrowski, Christopher C.
AU - Baskin, Ronald J.
AU - Kowalczykowski, Stephen C.
N1 - Funding Information:
We wish to thank Jason Bell, Aura Carreira, Petr Cejka, Anthony Forget, Joe Hilario, Taeho Kim, Hsu-Yang Lee, Katsumi Morimatsu, Amitabh Nimonkar, Behzad Rad, and Lisa Vancelette for their comments on this manuscript, and members of the Kowalczykowski lab for their contribution to this research. The research in our lab has been funded by grants from National Institutes of Health T32 CA-108459 to C. C. D., and GM-41347, GM-62653, and GM-64745 to S. C. K.
Publisher Copyright:
© 2010 Elsevier Inc.
PY - 2010/1
Y1 - 2010/1
N2 - 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.
AB - 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.
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U2 - 10.1016/S0076-6879(10)72007-3
DO - 10.1016/S0076-6879(10)72007-3
M3 - Chapter
C2 - 20580968
AN - SCOPUS:77957023630
T3 - Methods in Enzymology
SP - 261
EP - 291
BT - Methods in Enzymology
PB - Academic Press Inc.
ER -