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用具有宽敞微环境的共价有机框架胶囊来制造酶。

Fabricating Covalent Organic Framework Capsules with Commodious Microenvironment for Enzymes.

机构信息

State Key Laboratory of Medicinal Chemical biology, College of Pharmacy, Nankai University, Tianjin 300071, China.

Department of Chemical Sciences, Bernal Institute, University of Limerick, Limerick V94 T9PX, Republic of Ireland.

出版信息

J Am Chem Soc. 2020 Apr 8;142(14):6675-6681. doi: 10.1021/jacs.0c00285. Epub 2020 Mar 30.

Abstract

Enzyme immobilization has been demonstrated to be a favorable protocol to promote industrialization of biomacromolecules. Despite tremendous efforts to develop new strategies and materials to realize this process, maintaining enzyme activity is still a formidable challenge. Herein we created a sacrificial templating method, using metal-organic frameworks (MOFs) as sacrificial templates to construct hollow covalent organic framework (COF) capsules for enzyme encapsulation. This strategy can provide a capacious microenvironment to unleash enzyme molecules. The improved conformational freedom of enzymes, enhanced mass transfer, and protective effect against the external environment ultimately boosted the enzymatic activities. We also found that this strategy possesses high versatility that is suitable for diverse biomacromolecules, MOF templates, and COF capsules. Moreover, the dimensions, pore sizes, and shell thickness of COF capsules can be conveniently tuned, allowing for customizing bioreactors for specific functions. For example, coencapsulation of different enzymes with synergistic functions were successfully demonstrated using this bioreactor platform. This study not only opens up a new avenue to overcome the present limitations of enzymatic immobilization in porous matrixes but also provides new opportunities for construction of biomicrodevices or artificial organelles based on crystalline porous materials.

摘要

酶固定化已被证明是促进生物大分子工业化的一种有利方案。尽管人们付出了巨大的努力来开发新的策略和材料来实现这一过程,但保持酶的活性仍然是一个巨大的挑战。在这里,我们创建了一种牺牲模板法,使用金属有机框架(MOFs)作为牺牲模板来构建用于酶封装的中空共价有机框架(COF)胶囊。该策略可以提供一个宽敞的微环境来释放酶分子。酶的构象自由度的提高、传质的增强以及对外部环境的保护作用最终提高了酶的活性。我们还发现,该策略具有高度的通用性,适用于各种生物大分子、MOF 模板和 COF 胶囊。此外,COF 胶囊的尺寸、孔径和壳厚可以方便地调节,从而可以为特定功能定制生物反应器。例如,使用该生物反应器平台成功地证明了具有协同功能的不同酶的共包封。这项研究不仅为克服酶在多孔基质中固定化的当前限制开辟了新途径,而且为基于结晶多孔材料构建生物微器件或人工细胞器提供了新的机会。

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