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Published on: October 15, 2019
Dye-cycling DNA origami rotors for long-term tracking of transcription at base-pair resolution
Amanda L Wacker1, Ryan J Fantasia1, Brian Tenner2
1Department of Molecular Biology, University of California, San Diego, 9500 Gillman Drive, La Jolla, CA 92093, USA; Salk Institute for Biological Studies, 10010 N Torrey Pines Road, La Jolla, CA 92037, USA.
Abstract:
Protein-DNA interactions often result in rotational movements. These movements underlie many genetic processes such as DNA transcription by RNA polymerases (RNAPs). To illuminate these movements, we previously developed origami-rotor-based imaging and tracking (ORBIT), a fluorescence-based method that enables high-speed tracking of DNA rotation. When used to track DNA rotation during transcription by E. coli RNAP, ORBIT enabled the detection of single base-pair steps. However, the duration of ORBIT experiments was limited due to fluorescence photobleaching. To overcome this limitation and extend the total possible observation time, we here introduce dye-cycling ORBIT (dcORBIT), a method that enables observation of protein-DNA interactions for over 10 min at 20 Hz while maintaining single-base-pair precision. dcORBIT thereby opens new possibilities to study the fundamental rotational movements underlying gene expression.

