Jiangsu Key Laboratory of Biofunctional Materials, Jiangsu Collaborative Innovation Center of Biomedical Functional Materials, College of Chemistry and Materials Science, Nanjing Normal University , Nanjing, 210023, China.
Department of Chemistry, Texas A&M University , College Station, Texas 77843-3255, United States.
J Am Chem Soc. 2017 Jun 21;139(24):8312-8319. doi: 10.1021/jacs.7b03450. Epub 2017 Jun 7.
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)(OTf) nanosheets, while Zn(bim) 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.
二维金属有机骨架(MOF)纳米片可用作有效的酶抑制剂,为增强对细胞过程的控制以及增进对 MOF 和酶之间表面化学的理解提供了一种有启发性的方法。在本文中,我们证明了α-糜蛋白酶(ChT)的活性可以通过二维 Cu(bpy)(OTf)纳米片有效地抑制,达到 96.9%的抑制率,而 Zn(bim)纳米片对 ChT 没有显著的抑制作用。动力学研究表明,该材料对 ChT 起竞争性抑制剂的作用。此外,荧光和圆二色性光谱揭示二维 MOF 纳米片不会改变酶的二级结构。二维纳米片的 Cu(II)中心结合缓冲液中的 4-(2-羟乙基)-1-哌嗪乙磺酸(HEPES)分子,导致纳米片与酶之间的静电相互作用。此外,Cu(II)中心与 His-57 之间的不可逆配位相互作用在抑制过程中起重要作用,这得到离子强度实验和 Cu(II)d-d 跃迁的紫外吸收变化的支持。结果,底物被阻止到达酶的活性部位,从而导致酶抑制。二维 MOF 纳米片对酶活性的调节为探索生理和催化系统中 MOF-生物界面开辟了新的方向。