A molecular rotor sensor for detecting mitochondrial viscosity in apoptotic cells by two-photon fluorescence lifetime imaging

Impairing mitochondrial function may change its viscosity. The detection of changes in the mitochondrial viscosity is of great significance for biomedical research. Herein, we have designed a D-π-A type two-photon fluorescent probe ((4-(bis(4-(pyridin-4-yl)phenyl)amino)styryl)-1-methylpyridin-1-ium...

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Bibliographic Details
Published in:New journal of chemistry 2020-07, Vol.44 (26), p.11342-11348
Main Authors: Hou, Ming-Xuan, Liu, Liu-Yi, Wang, Kang-Nan, Chao, Xi-Juan, Liu, Rong-Xue, Mao, Zong-Wan
Format: Article
Language:English
Subjects:
Apoptosis
Biocompatibility
Cells (biology)
Change detection
Fluorescent indicators
Microscopy
Mitochondria
Photons
Viscosity
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Summary:Impairing mitochondrial function may change its viscosity. The detection of changes in the mitochondrial viscosity is of great significance for biomedical research. Herein, we have designed a D-π-A type two-photon fluorescent probe ((4-(bis(4-(pyridin-4-yl)phenyl)amino)styryl)-1-methylpyridin-1-ium iodide) ( DPTPA-Py ) with a triphenylamine derivative as the electron donor and pyridinium as the electron acceptor for detecting mitochondrial viscosity in living cells. It is found that both fluorescence intensity and fluorescence lifetime of DPTPA-Py are viscosity-dependent, and the probe exhibits a strong anti-interference ability in the detection of viscosity. The colocalization experiments reveal that DPTPA-Py is located in mitochondria only and is highly biocompatible. The probe shows no significant effects on the mitochondrial membrane potential. In addition, the probe is successfully used to monitor mitochondrial viscosity changes during apoptosis of living cells by two-photon microscopy (TPM) and fluorescence lifetime imaging microscopy (FLIM). A two-photon fluorescent probe was developed for detecting mitochondrial viscosity during apoptosis of living cells by two-photon microscopy (TPM) and fluorescence lifetime imaging microscopy (FLIM) with good selectivity and highly biocompatible.
ISSN:1144-0546
1369-9261
DOI:10.1039/d0nj02108c