Citation: Yan-Fen FANG, Yu-Ting HE, Li ZHAO, Hui-Bin NIU, Chun-Cheng CHEN, Yue LI, Ying-Ping HUANG. A Zn(Ⅱ) metal-organic framework as a matrix metalloproteinase mimic to catalyze the hydrolysis of microcystin-LR[J]. Chinese Journal of Inorganic Chemistry, ;2023, 39(12): 2265-2278. doi: 10.11862/CJIC.2023.205 shu

A Zn(Ⅱ) metal-organic framework as a matrix metalloproteinase mimic to catalyze the hydrolysis of microcystin-LR

Yan-Fen FANG ^{1, 2} ,
Yu-Ting HE ^{1, 2} ,
Li ZHAO ³ ,
Hui-Bin NIU ² ,
Chun-Cheng CHEN ⁴ ,
Yue LI ^3,, ,
Ying-Ping HUANG ^2,,

1.
College of Materials and Chemical Engineering, China Three Gorges University, Yichang, Hubei 443002, China
2.
Engineering Research Center of Eco-environment in Three Gorges Reservoir Region, Ministry of Education, Three Gorges University, Yichang, Hubei 443002, China
3.
College of Chemistry, Nankai University, Tianjin 300071, China
4.
Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China

Corresponding author: Yue LI, liyue84@nankai.edu.cn Ying-Ping HUANG, chem_ctgu@126.com
Received Date: 30 June 2023
Revised Date: 2 November 2023

Figures(7)

Constructed by the ligands of 3-amino-1,2,4-triazole-5-carboxylic acid (Hatz) and 1,3,5-benzenetricarboxylic acid (H₃btc), a Zn(Ⅱ) metal-organic framework with nanosheet morphology (Zn-MOF-1-NS) was prepared to mimic the structures of matrix metalloproteinases (MMPs). Zn-MOF-1-NS was highly effective in catalyzing the hydrolysis of the peptide bonds of microcystin (MC-LR). Within just 7.5 h, 82.6% of MC-LR was hydrolyzed (k=0.23 h^-1), which was much higher than the reported best hydrolysis efficiency of siderite (k=0.04 h^-1). This research has found that even when the amount of humic acid was increased tenfold, it did not significantly impede MC-LR decomposition. This demonstrates the impressive ability of the catalyst to resist interference from natural organic matter (NOM). Through in-situ attenuated total reflectance Fourier transform infrared spectroscopy (in-situ ATR-FTIR) and X-ray photoelectron spectroscopy (XPS) analyses, theoretical calculations, and comparison with a non-carboxyl counterpart, it was discovered that the surficial Zn(Ⅱ) site and the carboxyl group of Zn-MOF-1-NS participate in the cleavage of the peptide bond.
- microcystin-LR,
- selective hydrolysis,
- enzyme mimicking,
- metal-organic framework,
- matrix metalloproteinase
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