Truncated tetrahedral RNA nanostructures exhibit enhanced features for delivery of RNAi substrates.
Cell Cycle Proteins
/ chemistry
Cell Line, Tumor
Cryoelectron Microscopy
DEAD-box RNA Helicases
/ chemistry
Green Fluorescent Proteins
/ chemistry
Humans
Light
Molecular Dynamics Simulation
Nanostructures
/ chemistry
Nucleic Acid Conformation
Particle Size
Polymerase Chain Reaction
Protein Conformation
Protein Serine-Threonine Kinases
/ chemistry
Proto-Oncogene Proteins
/ chemistry
RNA
/ chemistry
RNA Interference
RNA, Small Interfering
Ribonuclease III
/ chemistry
Scattering, Radiation
Software
Thermodynamics
Polo-Like Kinase 1
Journal
Nanoscale
ISSN: 2040-3372
Titre abrégé: Nanoscale
Pays: England
ID NLM: 101525249
Informations de publication
Date de publication:
28 Jan 2020
28 Jan 2020
Historique:
pubmed:
15
1
2020
medline:
15
12
2020
entrez:
15
1
2020
Statut:
ppublish
Résumé
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.
Substances chimiques
Cell Cycle Proteins
0
Proto-Oncogene Proteins
0
RNA, Small Interfering
0
Green Fluorescent Proteins
147336-22-9
RNA
63231-63-0
Protein Serine-Threonine Kinases
EC 2.7.11.1
DICER1 protein, human
EC 3.1.26.3
Ribonuclease III
EC 3.1.26.3
DEAD-box RNA Helicases
EC 3.6.4.13
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM