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Two-Dimensional Metal–Organic Framework Nanosheets as an Enzyme Inhibitor: Modulation of the α-Chymotrypsin Activity

Xu, Ming, Yuan, Shuai, Chen, Xin-Yu, Chang, Yu-Jie, Day, Gregory, Gu, Zhi-Yuan, Zhou, Hong-Cai·2017·Journal of the American Chemical Society

Abstract

Two-dimensional metal–organic framework (MOF) nanosheets are utilized as effective enzyme inhibitors, providing an inspiring means to enhance the control of cellular processes as well as improve our understanding of the surface chemistry between MOFs and enzymes. In this paper, we demonstrated that the activity of α-chymotrypsin (ChT) can be effectively inhibited with 96.9% inhibition by 2-D Cu(bpy) 2 (OTf) 2 nanosheets, while Zn 2 (bim) 4 nanosheets show no significant inhibition effect toward ChT. Kinetic studies revealed that the material acts as a competitive inhibitor toward ChT. Furthermore, fluorescence and circular dichroism spectroscopy reveal that the 2-D MOF nanosheets do not change the secondary structure of the enzyme. The Cu(II) center of the 2-D nanosheets binds the 4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid (HEPES) molecules in the buffer, leading to an electrostatic interaction between the nanosheets and the enzyme. In addition, the irreversible coordination interactions between Cu(II) center and His-57 played an important role during the inhibition process, as supported by ionic strength experiments and UV absorbance changes of Cu(II) d–d transitions. As a result, the substrate is prevented from reaching the active sites of the enzyme causing enzyme inhibition. The modulation of enzyme activity by 2-D MOF nanosheets opens up a new direction for the exploration of the MOF–bio interface in physiological and catalytic systems.

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Metadata

Authors
Xu, M., Yuan, S., Chen, X.-Y., Chang, Y.-J., Day, G., Gu, Z.-Y., & Zhou, H.-C.
Venue
Journal of the American Chemical Society
Published
2017-06-07
Volume
139
Issue
24
Pages
8312-8319
ISSN
  • 0002-7863 (ISSN-L)
  • 1520-5126
OpenAlex
W2617943034
Cited by
185
References
1
FWCI
10.15
Type
journal article
Language
en
Open access
closed

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