DNA Looping in Topologically Constrained Domains

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Abstract

New techniques are needed in order to study the effects of DNA supercoiling on loop-mediated regulation. The thermodynamics of DNA looping depend periodically on the helical phasing between recognition sites. A long-term goal is to provide enabling technologies for ensemble and single-molecule FRET studies of DNA looping mediated by lac repressor in vitro and in vivo. Other applications of the methodology include engineering of DNA substrates for studies of site-specific recombination and other enzyme systems

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Keywords

DNA, Fluorescence resonance energy transfer, Recombination, genetic, DNA-protein interactions

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This work was supported by grants from the DMS/NIGMS Joint Program in Mathematical Biology (GM67242 and DMS-800929).

Rights

CC BY-NC 3.0 (Attribution-NonCommercial), ©2012 The Authors

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