Modular Assembly of a Concatenated DNA Circuit for In Vivo Amplified Aptasensing.


Journal

Small (Weinheim an der Bergstrasse, Germany)
ISSN: 1613-6829
Titre abrégé: Small
Pays: Germany
ID NLM: 101235338

Informations de publication

Date de publication:
05 2022
Historique:
revised: 09 04 2022
received: 15 02 2022
pubmed: 24 4 2022
medline: 28 5 2022
entrez: 23 4 2022
Statut: ppublish

Résumé

Probing endogenous molecular profiles in living entities is of fundamental significance to decipher biological functions and exploit novel theranostics. Despite programmable nucleic acid-based aptasensing systems across the breadth of molecular imaging, an aptasensing system enabling in vivo imaging with high sensitivity, accuracy, and adaptability is highly required yet is still in its infancy. Artificial catalytic DNA circuits that can modularly integrate to generate multiple outputs from a single input in an isothermal autonomous manner, have supplemented powerful toolkits for intracellular biosensing research. Herein, a multilayer nonenzymatic catalytic DNA circuits-based aptasensing system is devised for in situ imaging of a bioactive molecule in living mice by assembling branched DNA copolymers with high-molecular-weight and high-signal-gain based on avalanche-mimicking hybridization chain reactions (HCRs). The HCRs aptasensing circuit performs as a general and powerful sensing platform for precise analysis of a series of bioactive molecules due to its inherent rich recognition repertoire and hierarchical reaction accelerations. With tumor-targeting capsule encapsulation, the HCRs aptasensing circuit is specifically delivered into tumor cells and allowed the high-contrast imaging of intracellular adenosine triphosphate in living mice, highlighting its potential for visualizing these clinically important biomolecules and for studying the associated physiological processes.

Identifiants

pubmed: 35460185
doi: 10.1002/smll.202200983
doi:

Substances chimiques

DNA, Catalytic 0
DNA, Concatenated 0
DNA 9007-49-2

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e2200983

Informations de copyright

© 2022 Wiley-VCH GmbH.

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Auteurs

Qiong Wu (Q)

College of Chemistry and Molecular Sciences, Wuhan University, Wuhan, 430072, P. R. China.
Medical College, Wuhan University of Science and Technology, Wuhan, 430065, P. R. China.

Lei Yang (L)

College of Chemistry and Molecular Sciences, Wuhan University, Wuhan, 430072, P. R. China.

Lingling Xie (L)

Medical College, Wuhan University of Science and Technology, Wuhan, 430065, P. R. China.

Jinhua Shang (J)

College of Chemistry and Molecular Sciences, Wuhan University, Wuhan, 430072, P. R. China.

Shizhen He (S)

College of Chemistry and Molecular Sciences, Wuhan University, Wuhan, 430072, P. R. China.

Jing Liu (J)

Department of Gastroenterology, Hubei Clinical Center & Key Lab of Intestinal & Colorectal Diseases, Zhongnan Hospital of Wuhan University, Wuhan, 430072, P. R. China.

Fuan Wang (F)

College of Chemistry and Molecular Sciences, Wuhan University, Wuhan, 430072, P. R. China.

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