Directing Uphill Strand Displacement with an Engineered Superhelicase

The ability to finely tune reaction rates and binding energies between components has made DNA strand displacement circuits promising candidates to replicate the complex regulatory functions of biological reaction networks. However, these circuits often lack crucial properties, such as signal turnov...

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Bibliographic Details
Published inACS synthetic biology Vol. 12; no. 11; pp. 3424 - 3432
Main Authors Hall-Thomsen, Helena, Small, Shavier, Gavrilov, Momcilo, Ha, Taekjip, Schulman, Rebecca, Moerman, Pepijn Gerben
Format Journal Article
LanguageEnglish
Published United States American Chemical Society 17.11.2023
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Summary:The ability to finely tune reaction rates and binding energies between components has made DNA strand displacement circuits promising candidates to replicate the complex regulatory functions of biological reaction networks. However, these circuits often lack crucial properties, such as signal turnover and the ability to transiently respond to successive input signals that require the continuous input of chemical energy. Here, we introduce a method for providing such energy to strand displacement networks in a controlled fashion: an engineered DNA helicase, Rep-X, that transiently dehybridizes specific DNA complexes, enabling the strands in the complex to participate in downstream hybridization or strand displacement reactions. We demonstrate how this process can direct the formation of specific metastable structures by design and that this dehybridization process can be controlled by DNA strand displacement reactions that effectively protect and deprotect a double-stranded complex from unwinding by Rep-X. These findings can guide the design of active DNA strand displacement regulatory networks, in which sustained dynamical behavior is fueled by helicase-regulated unwinding.
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USDOE
SC0010426
ISSN:2161-5063
2161-5063
DOI:10.1021/acssynbio.3c00452