A highly selective ratiometric fluorescent probe for in vitro monitoring and cellular imaging of human carboxylesterase 1

被引:104
作者
Liu, Zhao-Ming [1 ]
Feng, Lei [2 ]
Ge, Guang-Bo [1 ]
Lv, Xia [1 ]
Hou, Jie [3 ]
Cao, Yun-Feng [1 ]
Cui, Jing-Nan [2 ]
Yang, Ling [1 ]
机构
[1] Chinese Acad Sci, Dalian Inst Chem Phys, Lab Pharmaceut Resource Discovery, Dalian 116023, Peoples R China
[2] Dalian Univ Technol, State Key Lab Fine Chem, Dalian 116012, Peoples R China
[3] Dalian Med Univ, Dalian 116044, Peoples R China
关键词
Ratiometric fluorescent probe; Human carboxylesterase 1; Large emission shift; Cell imaging; ESTER HYDROLASE 1; HUMAN LIVER; MAMMALIAN CARBOXYLESTERASES; DRUG-METABOLISM; LIVING CELLS; HYDROLYSIS; CLOPIDOGREL; BINDING; OSELTAMIVIR; ACTIVATION;
D O I
10.1016/j.bios.2014.01.049
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
A new ratiometric fluorescent probe derived from 2-(2-hydroxy-3-methoxyphenyl) benzothiazole (HMBT) has been developed for selective monitoring of human carboxylesterase 1 (hCE1). The probe is designed by introducing benzoyl moiety to HMBT. The prepared latent spectroscopic probe 1 displays satisfying stability under physiological pH conditions with very low background signal. Both the reaction phynotyping and chemical inhibition assays demonstrated that hCE1 mediated the specific cleavage of the carboxylic ester bond of probe 1 in human biological samples. The release of HMBT leads to a remarkable red-shifted emission in fluorescence spectrum (120 nm large emission shift). Furthermore, human cell-based assays show that probe 1 is cell membrane permeable, and it can be used for bioassay and cellular imaging of hCE1 activity in HepG2 cells. These findings lead to the development of a simple and sensitive fluorescent method for measurement of hCE1 activity in vitro or in living cells, in the presence of additional enzymes or endogenous compounds. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:30 / 35
页数:6
相关论文
共 49 条
[1]   Multisite promiscuity in the processing of endogenous substrates by human carboxylesterase 1 [J].
Bencharit, Sompop ;
Edwards, Carol C. ;
Morton, Christopher L. ;
Howard-Williams, Escher L. ;
Kuhn, Peter ;
Potter, Philip M. ;
Redinbo, Matthew R. .
JOURNAL OF MOLECULAR BIOLOGY, 2006, 363 (01) :201-214
[2]  
Brzezinski MR, 1997, DRUG METAB DISPOS, V25, P1089
[3]  
Choi JY, 2013, BIOSENS BIOELECTRON, V49, P438, DOI [10.1016/j.bios.013.05.033, 10.1016/j.bios.2013.05.033]
[4]   Inhibition of carboxylesterase 1 is associated with cholesteryl ester retention in human THP-1 monocyte/macrophages [J].
Crow, J. Allen ;
Middleton, Brandy L. ;
Borazjani, Abdolsamad ;
Hatfield, M. Jason ;
Potter, Philip M. ;
Ross, Matthew K. .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS, 2008, 1781 (10) :643-654
[5]   Selective and sensitive detection and quantification of arylamine N-acetyltransferase 2 by a ratiometric fluorescence probe [J].
Cui, Lei ;
Zhong, Ye ;
Zhu, Weiping ;
Xu, Yufang ;
Qian, Xuhong .
CHEMICAL COMMUNICATIONS, 2010, 46 (38) :7121-7123
[6]  
Demchenko AP, 2010, SPRINGER SER FLUORES, V8, P3, DOI 10.1007/978-3-642-04702-2_1
[7]   Carboxylesterase 1 Gene Duplication and mRNA Expression in Adipose Tissue are Linked to Obesity and Metabolic Function [J].
Friedrichsen, Martin ;
Poulsen, Pernille ;
Wojtaszewski, Jorgen ;
Hansen, Peter Riis ;
Vaag, Allan ;
Rasmussen, Henrik Berg .
PLOS ONE, 2013, 8 (02)
[8]   Cholinesterases: New roles in brain function and in Alzheimer's disease [J].
Giacobini, E .
NEUROCHEMICAL RESEARCH, 2003, 28 (3-4) :515-522
[9]   A Possible Mechanism for the Differences in Efficiency and Variability of Active Metabolite Formation from Thienopyridine Antiplatelet Agents, Prasugrel and Clopidogrel [J].
Hagihara, Katsunobu ;
Kazui, Miho ;
Kurihara, Atsushi ;
Yoshiike, Michiharu ;
Honda, Kokichi ;
Okazaki, Osamu ;
Farid, Nagy A. ;
Ikeda, Toshihiko .
DRUG METABOLISM AND DISPOSITION, 2009, 37 (11) :2145-2152
[10]   Design and synthesis of an ER-specific fluorescent probe based on carboxylesterase activity with quinone methide cleavage process [J].
Hakamata, Wataru ;
Machida, Aki ;
Oku, Tadatake ;
Nishio, Toshiyuki .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2011, 21 (11) :3206-3209