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利用稳定的基于锆的金属有机骨架仿生矿化大酶。

Biomimetic Mineralization of Large Enzymes Utilizing a Stable Zirconium-Based Metal-Organic Frameworks.

机构信息

Department of Chemistry, Northwestern University, Evanston, Illinois 60208-3113, United States.

Department of Chemical Engineering, Northwestern University, Evanston, Illinois 60208-3113, United States.

出版信息

J Am Chem Soc. 2024 Feb 28;146(8):5108-5117. doi: 10.1021/jacs.3c07785. Epub 2024 Feb 17.

Abstract

Enzymes are natural catalysts for a wide range of metabolic chemical transformations, including selective hydrolysis, oxidation, and phosphorylation. Herein, we demonstrate a strategy for the encapsulation of enzymes within a highly stable zirconium-based metal-organic framework. UiO-66-F was synthesized under mild conditions using an enzyme-compatible amino acid modulator, serine, at a modest temperature in an aqueous solution. Enzyme@UiO-66-F biocomposites were then formed by an encapsulation route in which UiO-66-F grows around the enzymes and, consequently, provides protection for the enzymes. A range of enzymes, namely, lysozyme, horseradish peroxidase, and amano lipase, were successfully encapsulated within UiO-66-F. We further demonstrate that the resulting biocomposites are stable under conditions that could denature many enzymes. Horseradish peroxidase encapsulated within UiO-66-F maintained its biological activity even after being treated with the proteolytic enzyme pepsin and heated at 60 °C. This strategy expands the toolbox of potential metal-organic frameworks with different topologies or functionalities that can be used as enzyme encapsulation hosts. We also demonstrate that this versatile process of encapsulation of enzymes under mild conditions (i.e., submerged in water and at a modest temperature) can be generalized to encapsulate enzymes of various sizes within UiO-66-F while protecting them from harsh conditions (i.e., high temperatures, contact with denaturants or organic solvents).

摘要

酶是广泛的代谢化学反应的天然催化剂,包括选择性水解、氧化和磷酸化。在此,我们展示了一种在高度稳定的锆基金属有机骨架内封装酶的策略。UiO-66-F 在温和条件下使用酶相容的氨基酸调节剂丝氨酸,在水溶液中于适度温度下合成。然后通过封装途径形成酶@UiO-66-F 生物复合材料,其中 UiO-66-F 在酶周围生长,从而为酶提供保护。一系列酶,即溶菌酶、辣根过氧化物酶和 Amano 脂肪酶,成功地封装在 UiO-66-F 内。我们进一步证明,在可能使许多酶变性的条件下,所得生物复合材料是稳定的。即使在用蛋白酶胃蛋白酶处理并在 60°C 加热后,封装在 UiO-66-F 内的辣根过氧化物酶仍保持其生物活性。该策略扩展了具有不同拓扑结构或功能的潜在金属有机骨架的工具箱,可作为酶封装宿主。我们还证明,这种温和条件下(即在水中并在适度温度下)封装酶的通用过程可以推广到在 UiO-66-F 内封装各种大小的酶,同时保护它们免受恶劣条件(即高温、与变性剂或有机溶剂接触)的影响。

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