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Multilayer DNA Origami with Terminal Interfaces That Are Flat and Wide-Area.
Kilwing, Luzia; Lill, Pascal; Nathwani, Bhavik; Guerra, Richard; Benson, Erik; Liedl, Tim; Shih, William M.
Afiliación
  • Kilwing L; Faculty of Physics and Center for NanoScience (CeNS), Ludwig-Maximilians-University, Geschwister-Scholl-Platz 1, 80539 Munich, Germany.
  • Lill P; Department of Cancer Biology, Dana-Farber Cancer Institute; Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, Massachusetts 02115, United States.
  • Nathwani B; Department of Cancer Biology, Dana-Farber Cancer Institute; Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, Massachusetts 02115, United States.
  • Guerra R; Department of Cancer Biology, Dana-Farber Cancer Institute; Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, Massachusetts 02115, United States.
  • Benson E; Department of Cancer Biology, Dana-Farber Cancer Institute; Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, Massachusetts 02115, United States.
  • Liedl T; Department of Physics, University of Oxford, Clarendon Laboratory, Oxford OX1 3PU, United Kingdom.
  • Shih WM; The Kavli Institute for Nanoscience Discovery, University of Oxford, New Biochemistry Building, Oxford OX1 3PU, United Kingdom.
ACS Nano ; 18(1): 885-893, 2024 Jan 09.
Article en En | MEDLINE | ID: mdl-38109901
ABSTRACT
DNA origami is a popular nanofabrication strategy that employs self-assembly of a long single scaffold strand, typically less than 10 kilobases in length, with hundreds of shorter staple strands into a desired shape. In particular, origami arranged as a single-layer rectangle has proven popular as flat pegboards that can display functionalities at staple-strand breakpoints, off the sides of the constituent double helices, with a ∼5.3 nm rhombic-lattice spacing. For applications that demand tighter spacing, functionalities can be displayed instead on the termini of helices of multilayer DNA origami. However, pegboards with the greatest addressable surface area are often found to be the most versatile. Given the practical limitations of the length of the scaffold that can be easily realized, designs that minimize the length of each helix would have advantages for maximizing the number of helices and therefore the number of addressable pixels on each terminal surface. Here we present an architecture for multilayer DNA origami displaying flush terminal interfaces from over 200 helices that each are only 5.3 turns in length. We characterize an example using cryo-EM imaging paired with single-particle analysis for further analysis of the global structure.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: ADN / Nanoestructuras Idioma: En Revista: ACS Nano Año: 2024 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: ADN / Nanoestructuras Idioma: En Revista: ACS Nano Año: 2024 Tipo del documento: Article País de afiliación: Alemania