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CRISPR/Cas9-based coronal nanostructures for targeted mitochondria single molecule imaging

The biological state at the subcellular level is highly relevant to many diseases, and the monitoring of organelles such as mitochondria is crucial based on this. However, most DNA and protein based nanoprobes used for the detection of mitochondrial RNAs (mitomiRs) lack spatial selectivity, which le...

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Detalles Bibliográficos
Autores principales: Zhao, Xuan, Na, Na, Ouyang, Jin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9533423/
https://www.ncbi.nlm.nih.gov/pubmed/36320584
http://dx.doi.org/10.1039/d2sc03329a
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author Zhao, Xuan
Na, Na
Ouyang, Jin
author_facet Zhao, Xuan
Na, Na
Ouyang, Jin
author_sort Zhao, Xuan
collection PubMed
description The biological state at the subcellular level is highly relevant to many diseases, and the monitoring of organelles such as mitochondria is crucial based on this. However, most DNA and protein based nanoprobes used for the detection of mitochondrial RNAs (mitomiRs) lack spatial selectivity, which leads to inefficiencies in probe delivery and signal turn-on. Herein, we constructed a novel DNA nanoprobe named protein delivery nano-corona (PDNC) to improve the delivery efficiency of Cas protein, for spatially selective imaging of mitomiRs in living cells switched on by a CRISPR/Cas system. Combined with a single-molecule counting method, this strategy enables highly sensitive detection of low-abundance mitomiR. Therefore, the strategy in this work opens up new opportunities for cell identification, early clinical diagnosis, and research in biological behaviour at the subcellular level.
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spelling pubmed-95334232022-10-31 CRISPR/Cas9-based coronal nanostructures for targeted mitochondria single molecule imaging Zhao, Xuan Na, Na Ouyang, Jin Chem Sci Chemistry The biological state at the subcellular level is highly relevant to many diseases, and the monitoring of organelles such as mitochondria is crucial based on this. However, most DNA and protein based nanoprobes used for the detection of mitochondrial RNAs (mitomiRs) lack spatial selectivity, which leads to inefficiencies in probe delivery and signal turn-on. Herein, we constructed a novel DNA nanoprobe named protein delivery nano-corona (PDNC) to improve the delivery efficiency of Cas protein, for spatially selective imaging of mitomiRs in living cells switched on by a CRISPR/Cas system. Combined with a single-molecule counting method, this strategy enables highly sensitive detection of low-abundance mitomiR. Therefore, the strategy in this work opens up new opportunities for cell identification, early clinical diagnosis, and research in biological behaviour at the subcellular level. The Royal Society of Chemistry 2022-09-10 /pmc/articles/PMC9533423/ /pubmed/36320584 http://dx.doi.org/10.1039/d2sc03329a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Zhao, Xuan
Na, Na
Ouyang, Jin
CRISPR/Cas9-based coronal nanostructures for targeted mitochondria single molecule imaging
title CRISPR/Cas9-based coronal nanostructures for targeted mitochondria single molecule imaging
title_full CRISPR/Cas9-based coronal nanostructures for targeted mitochondria single molecule imaging
title_fullStr CRISPR/Cas9-based coronal nanostructures for targeted mitochondria single molecule imaging
title_full_unstemmed CRISPR/Cas9-based coronal nanostructures for targeted mitochondria single molecule imaging
title_short CRISPR/Cas9-based coronal nanostructures for targeted mitochondria single molecule imaging
title_sort crispr/cas9-based coronal nanostructures for targeted mitochondria single molecule imaging
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9533423/
https://www.ncbi.nlm.nih.gov/pubmed/36320584
http://dx.doi.org/10.1039/d2sc03329a
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AT nana crisprcas9basedcoronalnanostructuresfortargetedmitochondriasinglemoleculeimaging
AT ouyangjin crisprcas9basedcoronalnanostructuresfortargetedmitochondriasinglemoleculeimaging