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Modulating the Biofunctionality of Metal-Organic-Framework-Encapsulated Enzymes through Controllable Embedding Patterns.
Angewandte Chemie International Edition ( IF 16.1 ) Pub Date : 2019-11-21 , DOI: 10.1002/anie.201913231 Guosheng Chen 1 , Xiaoxue Kou 1 , Siming Huang 2 , Linjing Tong 1 , Yujian Shen 1 , Wangshu Zhu 2 , Fang Zhu 1 , Gangfeng Ouyang 1, 3
Angewandte Chemie International Edition ( IF 16.1 ) Pub Date : 2019-11-21 , DOI: 10.1002/anie.201913231 Guosheng Chen 1 , Xiaoxue Kou 1 , Siming Huang 2 , Linjing Tong 1 , Yujian Shen 1 , Wangshu Zhu 2 , Fang Zhu 1 , Gangfeng Ouyang 1, 3
Affiliation
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.
中文翻译:
通过可控的嵌入模式调节金属有机框架封装的酶的生物功能。
将酶嵌入到MOF中作为外骨骼(enzyme @ MOF)提供了新的机会来改善酶的固有易碎性,同时也为MOF赋予了新的生物功能。尽管嵌入MOF的酶具有显着的稳定性,但是MOF诱捕后的嵌入模式和酶生物功能的转化仅受到了有限的关注。在这里,我们揭示了嵌入模式如何影响ZIF-8中封装的酶的生物活性。当酶促ZIF-8快速成核驱动包封过程时,酶@MOF可以保持高活性。当封装是由缓慢的共沉淀驱动的,并且酶不参与ZIF-8的成核时,由于配体的展开和竞争性配位,酶@MOF趋于失活,2-甲基咪唑。可以通过化学修饰酶的氨基酸来调节这两种嵌入方式,从而调节其生物功能。
更新日期:2020-01-04
中文翻译:
通过可控的嵌入模式调节金属有机框架封装的酶的生物功能。
将酶嵌入到MOF中作为外骨骼(enzyme @ MOF)提供了新的机会来改善酶的固有易碎性,同时也为MOF赋予了新的生物功能。尽管嵌入MOF的酶具有显着的稳定性,但是MOF诱捕后的嵌入模式和酶生物功能的转化仅受到了有限的关注。在这里,我们揭示了嵌入模式如何影响ZIF-8中封装的酶的生物活性。当酶促ZIF-8快速成核驱动包封过程时,酶@MOF可以保持高活性。当封装是由缓慢的共沉淀驱动的,并且酶不参与ZIF-8的成核时,由于配体的展开和竞争性配位,酶@MOF趋于失活,2-甲基咪唑。可以通过化学修饰酶的氨基酸来调节这两种嵌入方式,从而调节其生物功能。