Meng Fanchen, Xu Cheng, Zhang Linghai, Huang Xiaohan, Zhang Xinglong, Zhang Wenlei, Luo Yongqi, Zhang Weina, Huang Wei, Huo Fengwei, Zhang Suoying
Key Laboratory of Flexible Electronics (KLOFE), Institute of Advanced Materials (IAM) & School of Flexible Electronics (Future Technologies), Nanjing Tech University, Nanjing 211816, P.R. China.
Research (Wash D C). 2024 Aug 9;7:0434. doi: 10.34133/research.0434. eCollection 2024.
Metal-organic frameworks (MOFs) have been widely considered as ideal platforms for the preparation of biomimetic catalysts, but it remains challenging to fabricate MOF-based enzyme-like catalysts with optimal activity. Here, we leverage the inherent flexibility of MOFs and propose a novel trans-functionalization strategy to construct a carbonic anhydrase (CA) mimic by the structural transformation from ZIF-L to ZIF-8. Theoretical and experimental results reveal that during the structural transformation, the hydroxyl group will preferentially coordinate with the interlayer Zn clusters to form the CA-like active center Zn-N-OH. Therefore, more accessible active centers are generated on the as-prepared ZIF-8-OH, resulting in substantially enhanced catalytic activity in the hydrolysis of -nitrophenyl acetate.
金属有机框架(MOFs)已被广泛认为是制备仿生催化剂的理想平台,但制备具有最佳活性的基于MOF的类酶催化剂仍然具有挑战性。在此,我们利用MOFs固有的灵活性,提出了一种新颖的转功能化策略,通过从ZIF-L到ZIF-8的结构转变来构建碳酸酐酶(CA)模拟物。理论和实验结果表明,在结构转变过程中,羟基将优先与层间锌簇配位,形成类CA活性中心Zn-N-OH。因此,在制备的ZIF-8-OH上产生了更多可及的活性中心,从而在对硝基苯乙酸酯的水解中显著提高了催化活性。