Title of article :
A specific probe for two-photon fluorescence lysosomal imaging
Author/Authors :
Wu، نويسنده , , Zhiguo and Tang، نويسنده , , Mingliang and Tian، نويسنده , , Tian and Wu، نويسنده , , Jianguo and Deng، نويسنده , , Yuanlin and Dong، نويسنده , , Xiaohu and Tan، نويسنده , , Zheng-Yu Weng، نويسنده , , Xiaocheng and Liu، نويسنده , , Zhihong and Wang، نويسنده , , Chunjiang and Zhou، نويسنده , , Xiang، نويسنده ,
Issue Information :
ماهنامه با شماره پیاپی سال 2011
Pages :
6
From page :
216
To page :
221
Abstract :
Lysosomes are vital organelles in physiological processes, as they receive and degrade macromolecules from the secretory and endocytic procedures. Evidences have shown that lysosomes were related to oncogenic activation and cancer progression, so lysosomes targeting and imaging probes make them convenient to be observed. In this study, a lysosome specific probe W-7 was designed and synthesized via convenient one-pot reaction and Heck reaction. This probe was derived from Trِgerʹs base with a dimethylaminomethyl end group. The optical properties of this compound were measured. W-7 also showed two-photon absorption (TPA) effect by using laser excitation at the wavelength of infrared light. In vivo experiment, W-7 showed high specificity and selectivity for lysosomes in living cells (HeLa cells, MRC-5 cells and NRK cells), compared with LT Red, GT Red and MT Red (R = 0.96). Two-photon fluorescence images of HeLa cells stained by W-7 were obtained. And high resolution 3D reconstruction of lysosomes in one HeLa cell was provided by using two-photon confocal microscopy. The anantioseparation of racemic W-7 was carried out by chiral-HPLC, and the two enantiomers showed no significant difference in lysosomes imaging.
Keywords :
two-photon , In vivo imaging , Lysosome , Fluorescence probe , confocal microscopy
Journal title :
Talanta
Serial Year :
2011
Journal title :
Talanta
Record number :
1663877
Link To Document :
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