A Two-Photon Fluorescent Probe for Specific Imaging of Furin Activity in Living Cells and Tissues

被引:7
|
作者
Liu Hongwen [1 ]
Zhu Longmin [1 ]
Lou Xiaofeng [1 ]
Yuan Lin [1 ]
Zhang Xiao-Bing [1 ]
机构
[1] Hunan Univ, State Key Lab Chemo Biosensing & Chemometr, Coll Chem & Chem Engn, Mol Sci & Biomed Lab MBL, Changsha 410082, Hunan, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
two-photon; fluorescent probe; furin; cancer; hypoxia; PROPROTEIN CONVERTASES; EXPRESSION; EMISSION;
D O I
10.6023/A20070323
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Furin, the most characteristic member of the proprotein convertase (PCs), has important biological functions. The expression level of furin is related to many diseases, for example, the occurrence and development of cancer is closely related to the expression level of furin. Although several small-molecule fluorescent probes for furin have been developed, which were designed based on near-infrared dye or one-photon dye. These probes exhibit low Stocks' shift or shallow penetration depth, which leading to self-quenching and strong interference. Two-photon fluorescent probes, which utilize two near-infrared photons as the excitation source, can overcome these problems. Herein, a furin-activatable two-photon fluorescent probe (Nap-F) was developed firstly that allowed for detection and imaging of furin in live cells and tumor tissues. Nap-F consists of a classical two-photon fluorophore (1,8-naphthalimide), a furin-particular polypeptide sequence RVRR and a self-eliminating linker. Nap-F is water-soluble and in a fluorescence-off state itself due to the inhibited intramolecular charge transfer (ICT). In the absence of furin, no noticeable fluorescence enhancement was detected, even over 3 days in buffer solution, indicating its good stability. Upon the conversion by furin, it displayed a dramatically fluorescence enhancement at 545 nm, and exhibits high specificity and sensitivity to furin. Nap-F was applied for visualizing the difference in the expression level of furin in various cells, demonstrating its capacity of distinguishing some cancer cells from normal cells. Furthermore, Nap-F was utilized to visualize the variation of furin expression level efficiently after immobilization of hypoxia-inducible factor-1 (HIF-1) by CoCl2, with the results indicating that there is a positive correlation between the expression level of furin and the degree of hypoxia in tumor cells. Owing to the excellent property of Nap-F, the probe was also successful utilized to imaging furin activity in tumor tissues. Thus, Nap-F is able to serve as a potential tool for better exploring the intrinsic link between hypoxic physiological environment and cellular carcinogenesis and detecting cancer in preclinical applications.
引用
收藏
页码:1240 / 1245
页数:6
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