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RNA-DNA fibers and polygons with controlled immunorecognition activate RNAi, FRET and transcriptional regulation of NF-B in human cells

  1. Author:
    Ke, Weina
    Hong, Enping
    Saito, Renata F.
    Rangel, Maria Cristina
    Wang, Jian
    Viard,Mathias
    Richardson, Melina
    Khisamutdinov, Emil F.
    Panigaj, Martin
    Dokholyan, Nikolay
    Chammas, Roger
    Dobrovolskaia, Marina A.
    Afonin, Kirill A.
  2. Author Address

    Univ North Carolina Charlotte, Dept Chem, Nanoscale Sci Program, Charlotte, NC 28223 USA.NCI, Nanotechnol Characterizat Lab, Canc Res Technol Program, Frederick Natl Lab Canc Res, Frederick, MD 21702 USA.Univ Sao Paulo, Fac Med, Dept Radiol & Oncol, Ctr Invest Translac Oncol LIM24, Sao Paulo, SP, Brazil.Inst Canc Estado Sao Paulo, Sao Paulo, SP, Brazil.Penn State Coll Med, Dept Biochem & Mol Biol, Dept Pharmacol, Hershey, PA 17033 USA.Leidos Biomed Res Inc, Frederick Natl Lab Canc Res, Canc & Inflammat Program, Basic Sci Program, Frederick, MD 21702 USA.Ball State Univ, Dept Chem, Muncie, IN 47306 USA.Pavol Jozef Safarik Univ Kosice, Fac Sci, Inst Biol & Ecol, Kosice, Slovakia.Univ North Carolina Charlotte, Ctr Biomed Engn & Sci, Charlotte, NC 28223 USA.
    1. Year: 2019
    2. Date: FEB 20
    3. Epub Date: 2018 12 04
  1. Journal: Nucleic acids research
  2. OXFORD UNIV PRESS,
    1. 47
    2. 3
    3. Pages: 1350-1361
  3. Type of Article: Article
  4. ISSN: 0305-1048
  1. Abstract:

    Nucleic acid-based assemblies that interact with each other and further communicate with the cellular machinery in a controlled manner represent a new class of reconfigurable materials that can overcome limitations of traditional biochemical approaches and improve the potential therapeutic utility of nucleic acids. This notion enables the development of novel biocompatible smart' devices and biosensors with precisely controlled physicochemical and biological properties. We extend this novel concept by designing RNA-DNA fibers and polygons that are able to cooperate in different human cell lines and that have defined immunostimulatory properties confirmed by ex vivo experiments. The mutual intracellular interaction of constructs results in the release of a large number of different siRNAs while giving a fluorescent response and activating NF-B decoy DNA oligonucleotides. This work expands the possibilities of nucleic acid technologies by (i) introducing very simple design principles and assembly protocols; (ii) potentially allowing for a simultaneous release of various siRNAs together with functional DNA sequences and (iii) providing controlled rates of reassociation, stabilities in human blood serum, and immunorecognition.

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External Sources

  1. DOI: 10.1093/nar/gky1215
  2. PMID: 30517685
  3. WOS: 000467960500028

Library Notes

  1. Fiscal Year: FY2018-2019
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