Enhancing the enzymatic inhibition performance of Cu-based metal-organic frameworks by shortening the organic ligands

被引:1
|
作者
Xu, Ming [1 ]
Liang, Hong [1 ]
Meng, Sha-Sha [1 ]
Gu, Zhi-Yuan [1 ]
机构
[1] Nanjing Normal Univ, Coll Chem & Mat Sci, Jiangsu Collaborat Innovat Ctr Biomed Funct Mat, Jiangsu Key Lab Biofunct Mat, Nanjing 210023, Peoples R China
基金
中国国家自然科学基金;
关键词
ALPHA-CHYMOTRYPSIN; NANOSHEETS; STABILITY;
D O I
10.1039/d1an00531f
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Creating more exposed active sites on the metal-organic framework (MOF) surface is crucial for enhancing the recognition ability of MOF artificial receptors. Here, a copper-based MOF Cu(im)(2) (im = imidazole) was utilized to act as an artificial receptor, inhibiting the activity of alpha-chymotrypsin. The shortest diazole ligand reduced the distance between regenerative copper sites, creating as many active sites as possible on the MOF unit surface. The amount of copper(ii) centers on the Cu(im)(2) surface was calculated to be 4.96 x 10(6) mu m(-2). Thus, Cu(im)(2) showed exceedingly higher inhibition performance than other copper-based MOFs. The ChT activity was almost inhibited (88.8%) after the incubation with only 20 mu g mL(-1) Cu(im)(2) for 10 min. The binding between ChT and Cu(im)(2) was very fast with high affinity. Further results proved that Cu(im)(2) inhibited the activity of ChT through electrostatic interactions and coordination interactions via the mixed inhibition mode. This strategy to use short ligands to create more active sites on the MOF surface provides a new direction to enhance the inhibition efficiency.
引用
收藏
页码:4235 / 4241
页数:7
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