Toehold-Mediated Shape Transition of Nucleic Acid Nanoparticles.


Journal

ACS applied materials & interfaces
ISSN: 1944-8252
Titre abrégé: ACS Appl Mater Interfaces
Pays: United States
ID NLM: 101504991

Informations de publication

Date de publication:
31 May 2023
Historique:
pmc-release: 31 05 2024
medline: 2 6 2023
pubmed: 19 5 2023
entrez: 19 5 2023
Statut: ppublish

Résumé

We introduce a toehold-mediated strand displacement strategy for regulated shape-switching of nucleic acid nanoparticles (NANPs) enabling their sequential transformation from triangular to hexagonal architectures at isothermal conditions. The successful shape transitions were confirmed by electrophoretic mobility shift assays, atomic force microscopy, and dynamic light scattering. Furthermore, implementation of split fluorogenic aptamers allowed for monitoring the individual transitions in real time. Three distinct RNA aptamers─malachite green (MG), broccoli, and mango─were embedded within NANPs as reporter domains to confirm shape transitions. While MG "lights up" within the square, pentagonal, and hexagonal constructs, the broccoli is activated only upon formation of pentagon and hexagon NANPs, and mango reports only the presence of hexagons. Moreover, the designed RNA fluorogenic platform can be employed to construct a logic gate that performs an AND operation with three single-stranded RNA inputs by implementing a non-sequential polygon transformation approach. Importantly, the polygonal scaffolds displayed promising potential as drug delivery agents and biosensors. All polygons exhibited effective cellular internalization followed by specific gene silencing when decorated with fluorophores and RNAi inducers. This work offers a new perspective for the design of toehold-mediated shape-switching nanodevices to activate different light-up aptamers for the development of biosensors, logic gates, and therapeutic devices in the nucleic acid nanotechnology.

Identifiants

pubmed: 37204867
doi: 10.1021/acsami.3c01604
pmc: PMC10331730
mid: NIHMS1911549
doi:

Substances chimiques

Nucleic Acids 0
RNA 63231-63-0
Oligonucleotides 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

25300-25312

Subventions

Organisme : CCR NIH HHS
ID : HHSN261200800001C
Pays : United States
Organisme : NCI NIH HHS
ID : HHSN261200800001E
Pays : United States
Organisme : NIBIB NIH HHS
ID : R15 EB031388
Pays : United States
Organisme : NIGMS NIH HHS
ID : R35 GM139587
Pays : United States

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Auteurs

Jordan Hartung (J)

Department of Chemistry, Ball State University, Muncie, Indiana 47306, United States.

Nathan McCann (N)

Department of Chemistry, Ball State University, Muncie, Indiana 47306, United States.

Erwin Doe (E)

Department of Chemistry, Ball State University, Muncie, Indiana 47306, United States.

Hannah Hayth (H)

Department of Chemistry, Ball State University, Muncie, Indiana 47306, United States.

Kheiria Benkato (K)

Department of Chemistry, Ball State University, Muncie, Indiana 47306, United States.

M Brittany Johnson (MB)

Department of Biology, University of North Carolina at Charlotte, Charlotte, North Carolina 28223, United States.

Mathias Viard (M)

Laboratory of Integrative Cancer Immunology, Center for Cancer Research, National Cancer Institute, Bethesda, Maryland 20892, United States.
Basic Science Program, Leidos Biomedical Research Inc. National Cancer Institute, National Institutes of Health, Frederick, Maryland 21702, United States.

Kirill A Afonin (KA)

Department of Chemistry, University of North Carolina at Charlotte, Charlotte, North Carolina 28223, United States.

Emil F Khisamutdinov (EF)

Department of Chemistry, Ball State University, Muncie, Indiana 47306, United States.

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Classifications MeSH