Imaging of lysosomal pH changes with a novel quinoline/benzothiazole probe

2018 ◽  
Vol 42 (16) ◽  
pp. 13479-13485 ◽  
Author(s):  
Li Fan ◽  
Ming Nan ◽  
Jinyin Ge ◽  
Xiaodong Wang ◽  
Bo Lin ◽  
...  

A fluorescent pH probe BTVQ for imaging lysosomal pH fluctuations in live cells and extreme acidity in E. coli cells.

The Analyst ◽  
2018 ◽  
Vol 143 (20) ◽  
pp. 5054-5060 ◽  
Author(s):  
Bo Lin ◽  
Li Fan ◽  
Jinyin Ge ◽  
Wenjia Zhang ◽  
Caihong Zhang ◽  
...  

A naphthalene-based fluorescent pH probe with a pKa of 8.8 for imaging mitochondrial pH changes in live cells.


2015 ◽  
Vol 3 (16) ◽  
pp. 3260-3266 ◽  
Author(s):  
Xiao-Fan Zhang ◽  
Tao Zhang ◽  
Shi-Li Shen ◽  
Jun-Ying Miao ◽  
Bao-Xiang Zhao
Keyword(s):  
Ph Probe ◽  

The ratiometric pH probe RNL was constructed by integrating the naphthalimide moiety as an FRET donor into the rhodamine moiety as an FRET acceptor. The probe with a pKa of 4.82 could detect pH in the range of 4.50–5.50, selectively stain lysosome and detect lysosomal pH changes.


2013 ◽  
Vol 1 (34) ◽  
pp. 4281 ◽  
Author(s):  
Li Fan ◽  
Qiaoling Liu ◽  
Dongtao Lu ◽  
Heping Shi ◽  
Yunfeng Yang ◽  
...  
Keyword(s):  

2020 ◽  
Vol 8 (7) ◽  
pp. 1466-1471 ◽  
Author(s):  
Xiaodong Wang ◽  
Li Fan ◽  
Yubin Wang ◽  
Caihong Zhang ◽  
Wenting Liang ◽  
...  

We report a red-emission fluorescent pH probe (RML) for visual monitoring of the lysosomal pH changes during autophagy in living cells.


Talanta ◽  
2021 ◽  
Vol 228 ◽  
pp. 122184
Author(s):  
Qingfeng Xia ◽  
Shumin Feng ◽  
Jiaxin Hong ◽  
Guoqiang Feng

2002 ◽  
Vol 65 (2) ◽  
pp. 251-259 ◽  
Author(s):  
SCOTT L. BURNETT ◽  
LARRY R. BEUCHAT

Confocal scanning laser microscopy (CSLM) was used to differentiate viable and nonviable cells of Escherichia coli O157:H7 on and in raw apple tissues following treatment with water and 200 or 2,000 ppm active chlorine solution. Whole unwaxed Red Delicious cultivar apples at 25°C were inoculated by dipping in a suspension of E. coli O157:H7 (8.48 log10 CFU/ml) at 4°C, followed by treatment in water or chlorine solution at 21°C for 2 min. The dead cells on and in apples were distinguished from live cells by treating tissue samples with SYTOX green nucleic acid stain. Viable and dead cells were then labeled with an antibody conjugated with a fluorescent dye (Alexa Fluor 594). The percentage of viable cells on the apple surface, as well as at various depths in surface and internal structures, was determined. The mean percentages of viable cells located at the sites after treatment with water or chlorinated water were in the following order, which also reflects the order of protection against inactivation: floral tube wall (20.5%) > lenticels (15.0%) > damaged cuticle surrounding puncture wounds (13.0%) > intact cuticle (8.1%). The location of viable cells within tissues was dependent on the structure. Except for lenticels, the percentage of viable cells increased as depth into the CSLM stacks increased, indicating that cells attached to subsurface structures were better protected against inactivation with chlorine than were cells located on exposed surfaces. Further research is warranted to investigate the efficacy of other chemical sanitizers, as well as that of surfactants and solvents in combination with sanitizers, in removing or killing E. coli O157:H7 lodged in protective structures on the surface and within tissues of apples.


2017 ◽  
Vol 5 (5) ◽  
pp. 988-995 ◽  
Author(s):  
Baoli Dong ◽  
Xuezhen Song ◽  
Xiuqi Kong ◽  
Chao Wang ◽  
Nan Zhang ◽  
...  

Lysosomal pH is closely related to the metastasis and apoptosis of cancer cells.


Talanta ◽  
2020 ◽  
Vol 209 ◽  
pp. 120549 ◽  
Author(s):  
Yaqi Dong ◽  
Haibin Xiao ◽  
Lingbao Xing ◽  
Chuanchen Wu ◽  
Jin Zhou ◽  
...  

Small ◽  
2012 ◽  
Vol 8 (6) ◽  
pp. 943-948 ◽  
Author(s):  
Pilar RiveraGil ◽  
Moritz Nazarenus ◽  
Sumaira Ashraf ◽  
Wolfgang J. Parak

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