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Fluorescence Resonance Energy Transfer over 130 Basepairs in Hyperstable Lac Repressor-DNA Loops

Department of Chemistry and Biochemistry, University of Maryland, College Park, College Park, Maryland 20742-2021 USA

Correspondence: Address reprint requests to Jason D. Kahn, Tel.: 301-405-0058; Fax: 301-405-9376; E-mail: kahn{at}adnadn.umd.edu.

Lac repressor (LacI) binds two operator DNA sites, looping the intervening DNA. DNA molecules containing two lac operators bracketing a sequence-directed bend were previously shown to form hyperstable LacI-looped complexes. Biochemical studies suggested that orienting the operators outward relative to the bend direction (in construct 9C14) stabilizes a positively supercoiled closed form, with a V-shaped LacI, but that the most stable loop construct (11C12) is a more open form. Here, fluorescence resonance energy transfer (FRET) is measured on DNA loops, between fluorescein and TAMRA attached near the two operators, 130 basepairs apart. For 9C14, efficient LacI-induced energy transfer (74% based on donor quenching) confirms that the designed DNA shape can force the looped complex into a closed form. From enhanced acceptor emission, correcting for observed donor-dependent quenching of acceptor fluorescence, 52% transfer was observed. Time-resolved FRET suggests that this complex exists in both closed- and open form populations. Less efficient transfer, 10%, was detected for DNA-LacI sandwiches and 11C12-LacI, consistent with an open form loop. This demonstration of long-range FRET in large DNA loops confirms that appropriate DNA design can control loop geometry. LacI flexibility may allow it to maintain looping with other proteins bound or under different intracellular conditions.

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