| Literature DB >> 31749284 |
Guosheng Chen1, Xiaoxue Kou1, Siming Huang2, Linjing Tong1, Yujian Shen1, Wangshu Zhu2, Fang Zhu1, Gangfeng Ouyang1,3.
Abstract
Embedding an enzyme within a MOF as exoskeleton (enzyme@MOF) offers new opportunities to improve the inherent fragile nature of the enzyme, but also to impart novel biofunctionality to the MOF. Despite the remarkable stability achieved for MOF-embedded enzymes, embedding patterns and conversion of the enzymatic biofunctionality after entrapment by a MOF have only received limited attention. Herein, we reveal how embedding patterns affect the bioactivity of an enzyme encapsulated in ZIF-8. The enzyme@MOF can maintain high activity when the encapsulation process is driven by rapid enzyme-triggered nucleation of ZIF-8. When the encapsulation is driven by slow coprecipitation and the enzymes are not involved in the nucleation of ZIF-8, enzyme@MOF tends to be inactive owing to unfolding and competing coordination caused by the ligand, 2-methyl imidazole. These two embedding patterns can easily be controlled by chemical modification of the amino acids of the enzymes, modulating their biofunctionality.Entities:
Keywords: biocatalysis; embedding patterns; enzyme immobilization; enzyme-surface modification; metal-organic frameworks
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Year: 2020 PMID: 31749284 DOI: 10.1002/anie.201913231
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336