Self-calibrated fluorescent probe resembled as an indicator of the lysosomal phosphatase pertaining to the cancer cells

被引:9
|
作者
Podder, Arup [1 ]
Alex, Susan M. [2 ]
Maiti, Mrinmoy [1 ]
Maiti, Kaustabh Kumar [2 ,3 ]
Bhuniy, Sankarprasad [1 ,4 ]
机构
[1] Amrita Univ, Amrita Ctr Ind Res & Innovat, Coimbatore 64112, Tamil Nadu, India
[2] CSIR NIIST, Chem Sci & Technol Div, Ind Estate, Thiruvananthapuram 695019, Kerala, India
[3] CSIR NIIST, AcSIR, Thiruvananthapuram 695019, Kerala, India
[4] Amrita Univ, Dept Chem Engn & Mat Sci, Coimbatore 641112, Tamil Nadu, India
关键词
Lysosomal phosphatase; Fluorescent; Naphthalimide; Chemoselective; Bioimaging; AGGREGATION-INDUCED EMISSION; LIGHT-UP PROBE; TURN-ON PROBE; ALKALINE-PHOSPHATASE; LIVING CELLS; ASSAY; TETRAPHENYLETHYLENE; STRATEGY;
D O I
10.1016/j.jphotobiol.2017.10.019
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A self-calibrated fluorescent probe Lyso-Phos has synthesized followed by a straightforward synthetic pathway. Lyso-Phos acts as an indicator for lysosomal phosphatase. Its photophysical property including cellular imaging was described. Lyso-Phos showed ratiometric UV-Vis- absorption changes from lambda(abs) 370 nm to lambda(abs) 450 nm in the presence of alkaline phosphatase (ALP). On the other hand, fluorescence intensity lambda(em) 560 nm of Lyso-Phos has increased around 45-fold in the presence of ALP. The probe Lyso-Phos was found to be highly chemoselective toward the phosphatase compared with other ubiquitous entities in cellular milieu. The non-toxic nature of the Lyso-phos has accounted by observing higher cell viability in prostate cancer- LnCap, fibrosarcoma HT1080 and normal mouse embryo fibroblast NIH3T3 cells. Further, the probe Lyso-Phos was utilized for tracking of cellular phosphatase in live-cells. Lyso-Phos enabled to track cellular phosphatase by the extent of fluorescence labeling of LnCap cells which showed reasonable uptake efficiency in the presence of Lyso Phos as indicated by the intracellular fluorescence. The phosphoester bond in the probe was cleaved by intracellular alkaline phosphatase leading to turn on fluorescence of the fluorescent probe Lyso Phos. Finally, cellular co-localization with Lyso-Tracker empowered our speculation that Lyso-Phos can track endogenous phosphatase in the lysosomes. Altogether these findings suggest that Lyso-Phos would be powerful probe to detect phosphates in cancer cells.
引用
收藏
页码:105 / 111
页数:7
相关论文
共 50 条
  • [31] Biocompatible fluorescent probe for detecting mitochondrial alkaline phosphatase activity in live cells
    Khatun, Sabina
    Biswas, Shayeri
    Mahanta, Arun Kumar
    Joseph, Manu M.
    Vidyalekshmi, Murukan S.
    Podder, Arup
    Maiti, Pralay
    Maiti, Kaustabh Kumar
    Bhuniya, Sankarprasad
    [J]. JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY B-BIOLOGY, 2020, 212
  • [32] A fluorescent probe for detection of an intracellular prognostic indicator in early-stage cancer
    Ji, Haiwei
    Guan, Yijia
    Wu, Li
    Ren, Jinsong
    Miyoshi, Daisuke
    Sugimoto, Naoki
    Qu, Xiaogang
    [J]. CHEMICAL COMMUNICATIONS, 2015, 51 (08) : 1479 - 1482
  • [33] A naphthalene-based fluorescent probe for ratiometric imaging of lysosomal hydrogen sulfide in living cells
    Gao, Cai
    Liu, Xianjun
    Chen, Wen
    Wang, Fenglin
    Jiang, Jian-Hui
    [J]. METHODS AND APPLICATIONS IN FLUORESCENCE, 2019, 7 (01):
  • [34] A lysosomal targeted fluorescent probe based on coumarin for monitoring hydrazine in living cells with high performance
    Jiang, Jin-Hua
    Zhang, Zhi-Hao
    Qu, Jianbo
    Wang, Jian-Yong
    [J]. ANALYTICAL METHODS, 2021, 14 (01) : 17 - 21
  • [35] Assessing effects of pressure on tumor and normal tissue physiology using an automated self-calibrated, pressure-sensing probe for diffuse reflectance spectroscopy
    Palmer, Gregory M.
    Zhang, Hengtao
    Lee, Chen-Ting
    Mikati, Husam
    Herbert, Joseph A.
    Krieger, Marlee
    von Windheim, Jesko
    Koester, Dave
    Stevenson, Daniel
    Rocke, Daniel J.
    Esclamado, Ramon
    Erkanli, Alaatin
    Ramanujam, Nirmala
    Dewhirst, Mark W.
    Lee, Walter T.
    [J]. JOURNAL OF BIOMEDICAL OPTICS, 2018, 23 (05)
  • [36] Imaging of lysosomal activity using naphthalimide-benzimidazole based fluorescent probe in living cells
    Sharma, Pooja
    Gupta, Neha
    Kaur, Sandeep
    Kaur, Satwinderjeet
    Ohri, Puja
    Parihar, Ripu D.
    Bhalla, Vandana
    Kumar, Manoj
    [J]. SENSORS AND ACTUATORS B-CHEMICAL, 2019, 286 : 451 - 459
  • [37] Dissecting lysosomal viscosity fluctuations in live cells and liver tissues with an ingenious NIR fluorescent probe
    Zhang, Yu
    Jiang, Qingqing
    Wang, Kai
    Fang, Yuqi
    Zhang, Peng
    Wei, Liangchen
    Li, Dongpeng
    Shu, Wei
    Xiao, Haibin
    [J]. TALANTA, 2024, 272
  • [38] Ratiometric emission NIR-fluorescent probe for the detection of lysosomal pH in living cells and in vivo
    Niu, Weifen
    Jia, Juan
    Li, Junkai
    Zhang, Chao
    Yun, Keming
    [J]. NEW JOURNAL OF CHEMISTRY, 2019, 43 (34) : 13363 - 13370
  • [39] A New Ratiometric Lysosomal Copper(II) Fluorescent Probe To Map a Dynamic Metallome in Live Cells
    Giuffrida, Maria Laura
    Sfrazzetto, Giuseppe Trusso
    Satriano, Cristina
    Zimbone, Stefania
    Tomaselli, Gaetano A.
    Copani, Agata
    Rizzarelli, Enrico
    [J]. INORGANIC CHEMISTRY, 2018, 57 (05) : 2365 - 2368
  • [40] Real-time visualization of lysosomal pH fluctuations in living cells with a ratiometric fluorescent probe
    Wang, Zhonglong
    Zhang, Yan
    Zhu, Yurong
    Fu, Yubin
    Zhang, Xinru
    Shen, Zheyu
    Gong, Shuai
    Meng, Zhiyuan
    Wang, Shifa
    [J]. MICROCHEMICAL JOURNAL, 2022, 180