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Protein-Assisted Room-Temperature Assembly of Rigid, Immobile Holliday Junctions and Hierarchical DNA Nanostructures

  1. Author:
    Ramakrishnan,Saminathan
    Subramaniam, Sivaraman
    Kielar, Charlotte
    Grundmeier, Guido
    Stewart, A. Francis
    Keller, Adrian
  2. Author Address

    Paderborn Univ, Tech & Macromol Chem, Warburger Str 100, D-33098 Paderborn, Germany.NCI, Struct Biophys Lab, Ctr Canc Res, Frederick, MD 21702 USA.Tech Univ Dresden, Biotechnol Ctr, Dept Genom, Tatzberg 47-51, D-01307 Dresden, Germany.Tech Univ Dresden, Cluster Excellence Phys Life, D-01062 Dresden, Germany.Helmholtz Zentrum Dresden Rossendorf, Inst Resource Ecol, Bautzner Landstr 400, D-01328 Dresden, Germany.
    1. Year: 2020
    2. Date: NOV
  1. Journal: MOLECULES
  2. MDPI,
    1. 25
    2. 21
  3. Type of Article: Article
  4. Article Number: 5099
  5. ISSN: 1420-3049
  1. Abstract:

    Immobile Holliday junctions represent not only the most fundamental building block of structural DNA nanotechnology but are also of tremendous importance for the in vitro investigation of genetic recombination and epigenetics. Here, we present a detailed study on the room-temperature assembly of immobile Holliday junctions with the help of the single-strand annealing protein Red beta. Individual DNA single strands are initially coated with protein monomers and subsequently hybridized to form a rigid blunt-ended four-arm junction. We investigate the efficiency of this approach for different DNA/protein ratios, as well as for different DNA sequence lengths. Furthermore, we also evaluate the potential of Red beta to anneal sticky-end modified Holliday junctions into hierarchical assemblies. We demonstrate the Red beta-mediated annealing of Holliday junction dimers, multimers, and extended networks several microns in size. While these hybrid DNA-protein nanostructures may find applications in the crystallization of DNA-protein complexes, our work shows the great potential of Red beta to aid in the synthesis of functional DNA nanostructures under mild reaction conditions.

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External Sources

  1. DOI: 10.3390/molecules25215099
  2. WOS: 000589351000001

Library Notes

  1. Fiscal Year: FY2020-2021
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