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Design and development of fluorescent probe substrates for carboxylesterase 1 using BODIPY as the basic fluorophore
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Le-le DING1, 2, Zhen-hao TIAN1, Jie HOU1, 3, Zi-miao WENG3, Jing-nan CUI1, Ling YANG2, Guang-bo GE2, *
Acta Pharmaceutica Sinica | 2017, 52(1) : 58 - 65
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Acta Pharmaceutica Sinica | 2017, 52(1): 58-65
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Design and development of fluorescent probe substrates for carboxylesterase 1 using BODIPY as the basic fluorophore
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Le-le DING1, 2, Zhen-hao TIAN1, Jie HOU1, 3, Zi-miao WENG3, Jing-nan CUI1, Ling YANG2, Guang-bo GE2, *
Affiliations
  • 1. State Key Laboratory of Fine Chemicals, Dalian University of Technology, Dalian 116023, China
  • 2. Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, China
  • 3. Dalian Medical University, Dalian 116011, China
Published: 2017-01-12 doi: 10.16438/j.0513-4870.2016-1004
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Carboxylesterase 1 (CE1) is an important serine hydrolase in mammals, which involved in the hydrolysis of a variety of compounds (endogenous substrates like cholesterol and xenobiotic compounds like ester-contain drugs and pesticides). This study aimed to design and develop the fluorescent probe substrates for human carboxylesterase 1 (hCE1), on the basis of the structural features of hCE1 preferred substrates. Four carboxylic esters deriving from BODIPY-8-carboxylic acid were designed and synthesized. After then, reaction phenotyping assays and chemical inhibition assays were used to evaluate the selectivity of these four ester derivatives towards hCE1. Our results clearly demonstrated that the substrate specificity of these ester substrates towards hCE1 would be improved with the decrease of the alcohol group on BODIPY-8-carboxylesters, while BODIPY-8-carboxylesters with small alcohol groups including methyl (BCM) and ethyl (BCE) esters could serve as the ideal probe substrates for hCE1. Given that BCM exhibit rapid hydrolytic rate in hCE1, we further investigate the enzymatic kinetics of this fluorescent probe substrate in both human liver microsomes (HLM) and recombinant hCE1, as well as to explore its potential application in high-throughput screening of hCE1 inhibitors by using HLM as enzyme source. The results showed that the kinetic behaviors and the affinity of BCM in HLM is much closed to those in recombinant hCE1, implying that hCE1 played the key roles in BCM hydrolysis in HLM. Furthermore, the inhibition study demonstrated that BCM could be used for rapid screening and characterization of hCE1 inhibitors, by using HLM to replace recombinant hCE1 as enzyme source.

carboxylesterase 1  /  boron-dipyrromethene  /  fluorescent probe  /  specificity  /  inhibitors screening
Le-le DING, Zhen-hao TIAN, Jie HOU, Zi-miao WENG, Jing-nan CUI, Ling YANG, Guang-bo GE. Design and development of fluorescent probe substrates for carboxylesterase 1 using BODIPY as the basic fluorophore[J]. Acta Pharmaceutica Sinica, 2017 , 52 (1) : 58 -65 . DOI: 10.16438/j.0513-4870.2016-1004
Year 2017 volume 52 Issue 1
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Article Info
doi: 10.16438/j.0513-4870.2016-1004
  • Receive Date:2016-10-17
  • Online Date:2026-01-14
  • Published:2017-01-12
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History
  • Received:2016-10-17
  • Revised:2016-12-07
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Affiliations
    1. State Key Laboratory of Fine Chemicals, Dalian University of Technology, Dalian 116023, China
    2. Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, China
    3. Dalian Medical University, Dalian 116011, China
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表12种不同金属材料的力学参数

Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)

Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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