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Truncated tetrahedral RNA nanostructures exhibit enhanced features for delivery of RNAi substrates.
Zakrevsky, Paul; Kasprzak, Wojciech K; Heinz, William F; Wu, Weimin; Khant, Htet; Bindewald, Eckart; Dorjsuren, Nomongo; Fields, Eric A; de Val, Natalia; Jaeger, Luc; Shapiro, Bruce A.
Afiliación
  • Zakrevsky P; RNA Biology Laboratory, National Cancer Institute, Frederick, MD 21702, USA. shapirbr@mail.nih.gov.
  • Kasprzak WK; Basic Science Program, Frederick National Laboratory for Cancer Research, Frederick, MD 21702, USA.
  • Heinz WF; Optical Microscopy and Analysis Laboratory, Cancer Research Technology Program, Frederick National Laboratory for Cancer Research, Frederick, MD 21702, USA.
  • Wu W; Center for Molecular Microscopy, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Frederick, MD 21702, USA.
  • Khant H; Center for Molecular Microscopy, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Frederick, MD 21702, USA.
  • Bindewald E; Basic Science Program, Frederick National Laboratory for Cancer Research, Frederick, MD 21702, USA.
  • Dorjsuren N; RNA Biology Laboratory, National Cancer Institute, Frederick, MD 21702, USA. shapirbr@mail.nih.gov.
  • Fields EA; RNA Biology Laboratory, National Cancer Institute, Frederick, MD 21702, USA. shapirbr@mail.nih.gov.
  • de Val N; Center for Molecular Microscopy, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Frederick, MD 21702, USA and Cancer Research Technology Program, Frederick National Laboratory for Cancer Research, Leidos Biomedical Research Inc, Frederick, MD 21701, USA.
  • Jaeger L; Department of Chemistry and Biochemistry, Biomolecular Science and Engineering Program, University of California, Santa Barbara, CA 93106-9510, USA. jaeger@chem.ucsb.edu.
  • Shapiro BA; RNA Biology Laboratory, National Cancer Institute, Frederick, MD 21702, USA. shapirbr@mail.nih.gov.
Nanoscale ; 12(4): 2555-2568, 2020 Jan 28.
Article en En | MEDLINE | ID: mdl-31932830
ABSTRACT
Using RNA as a material for nanoparticle construction provides control over particle size and shape at the nano-scale. RNA nano-architectures have shown promise as delivery vehicles for RNA interference (RNAi) substrates, allowing multiple functional entities to be combined on a single particle in a programmable fashion. Rather than employing a completely bottom-up approach to scaffold design, here multiple copies of an existing synthetic supramolecular RNA nano-architecture serve as building blocks along with additional motifs for the design of a novel truncated tetrahedral RNA scaffold, demonstrating that rationally designed RNA assemblies can themselves serve as modular pieces in the construction of larger rationally designed structures. The resulting tetrahedral scaffold displays enhanced characteristics for RNAi-substrate delivery in comparison to similar RNA-based scaffolds, as evidenced by its increased functional capacity, increased cellular uptake and ultimately an increased RNAi efficacy of its adorned Dicer substrate siRNAs. The unique truncated tetrahedral shape of the nanoparticle core appears to contribute to this particle's enhanced function, indicating the physical characteristics of RNA scaffolds merit significant consideration when designing platforms for delivery of functional RNAs via RNA nanoparticles.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: ARN / Interferencia de ARN / Ribonucleasa III / Nanoestructuras / ARN Helicasas DEAD-box Límite: Humans Idioma: En Revista: Nanoscale Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: ARN / Interferencia de ARN / Ribonucleasa III / Nanoestructuras / ARN Helicasas DEAD-box Límite: Humans Idioma: En Revista: Nanoscale Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos