journal article·2018-01

Utilizing HomoFRET to Extend DNA‐Scaffolded Photonic Networks and Increase Light‐Harvesting Capability

William P. Klein, Sebastián A. Díaz, Susan Buckhout‐White, Joseph S. Melinger, Paul D. Cunningham, Ellen R. Goldman, Mario G. Ancona, Wan Kuang, Igor L. Medintz

Advanced Optical Materials· Volume 6· Issue 1
Publisher page

Abstract

Abstract DNA‐based photonic wires that exploit Förster resonance energy transfer (FRET) between pendant fluorophores to direct and focus excitonic energy have high research interest due to their potential applications in light harvesting, biocomputing, and biosensing. One important goal with these structures is to increase their ability to harvest energy and then transfer it over multiple steps both across extended portions of the spectra and physical space. Toward these goals, incorporating extended homogeneous or homoFRET sections into three unique FRET cascade DNA dendrimer architectures are explored. The effects of inserting increasingly longer homoFRET modules into assemblies based on AF488→Cy3→Cy3.5→Cy5→Cy5.5 dye‐displaying four‐arm, eight‐arm, and 2:1 dendrimeric DNA photonic wires are evaluated to understand what these hybrid structures may offer toward increased efficiency. Each structure incorporates an extendable Cy3 homoFRET region capable of incorporating one to six Cy3 repeats. Steady‐state and time‐resolved fluorescence measurements along with detailed analysis and simulations reveal that despite their modest relay capabilities, the structures are capable of acting as efficient antennas, with the dendrimeric structure manifesting a remarkably high sixfold gain. Moreover, an energy transfer efficiency of ≈3% is possible over nine sequential FRET steps.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: Advanced biosensing and bioanalysis techniques · DNA and Nucleic Acid Chemistry · Molecular Junctions and Nanostructures

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Center for Bio/Molecular Science and Engineering, Code 6900 U.S. Naval Research Laboratory Washington DC 20375 USA

Electronics Science and Technology Division, Code 6800 U.S. Naval Research Laboratory Washington DC 20375 USA

Department of Electrical and Computer Engineering Boise State University Boise ID 83706 USA

Funding

U.S. Naval Research Laboratory · U.S. Nuclear Regulatory Commission

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