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Orthogonally-tunable and ER-targeting fluorophores detect avian influenza virus early infectionopen access

Authors
Kang, TaewonHaque, MamunulLee, BoranHong, Kyung TaeHong, Seong CheolKim, YounghunLee, JesangLee, Jun-SeokLee, Dongwhan
Issue Date
4-10월-2022
Publisher
NATURE PORTFOLIO
Citation
NATURE COMMUNICATIONS, v.13, no.1
Indexed
SCIE
SCOPUS
Journal Title
NATURE COMMUNICATIONS
Volume
13
Number
1
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/145671
DOI
10.1038/s41467-022-33586-1
ISSN
2041-1723
Abstract
Methods to detect and distinguish the early stage of viral infection often involve complicated and time-consuming protocols. Here, the authors disclose a class of fluorescent molecules that enable fast detection of avian influenza virus infection by selectively localizing at the endoplasmic reticulum in the cell. Cell-based assays can monitor virus infection at a single-cell level with high sensitivity and cost-efficiency. For this purpose, it is crucial to develop molecular probes that respond selectively to physiological changes in live cells. We report stimuli-responsive light-emitters built on a T-shaped benzimidazole platform, and consecutive borylation reactions to produce a library of homologs displaying systematic changes in fluorescence quantum yield and environmental sensitivity. We find that certain fluorophores localize selectively at the endoplasmic reticulum, and interact with proteins involved in the stress signaling pathways. Notably, the mono-borylated compound responds selectively to the stress conditions by enhancing fluorescence, and detects avian influenza virus infection at the single-cell level. Our findings demonstrate the unprecedented practical utility of the stress-responsive molecular probes to differentiate cellular states for early diagnosis.
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