碳酸酐酶
反应性(心理学)
化学
金属有机骨架
吸附
金属
组合化学
酶
有机化学
医学
病理
替代医学
作者
Ashley M. Wright,Zhenwei Wu,Guanghui Zhang,Jenna L. Mancuso,Robert J. Comito,Robert W. Day,Christopher H. Hendon,Jeffrey T. Miller,Mircea Dincă
出处
期刊:Chem
[Elsevier BV]
日期:2018-10-04
卷期号:4 (12): 2894-2901
被引量:116
标识
DOI:10.1016/j.chempr.2018.09.011
摘要
Metal-organic frameworks (MOFs) have exciting potential for biomimetic studies of enzymes, yet construction of high-fidelity models at the metal nodes is challenging. Nonetheless, biomimetic MOFs have significant advantages, such as increased stability and ease of separation, over their enzymatic and homogeneous counterparts, making them particularly attractive for industrial applications. Here, we demonstrate biomimetic behavior of Zn hydroxide moieties inside a MOF with structural and reactivity characteristics of carbonic anhydrase. Similar to the biological system, the MOF binds CO2 by an insertion mechanism into the Zn–OH bond, leading to significant adsorption of CO2 (3.41 mmol/g). In reactivity mimicking that of the enzyme, the material also catalyzes the oxygen isotope exchange between water and carbon dioxide. Overall, these results provide the strongest evidence yet of metal nodes in MOFs bearing high structural fidelity to enzymatic active sites.
科研通智能强力驱动
Strongly Powered by AbleSci AI