将生物催化剂融入金属有机框架:厘清亲和力、分子量和尺寸的作用。

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
ACS Applied Bio Materials Pub Date : 2024-11-04 Epub Date: 2024-10-24 DOI:10.1002/cbic.202400625
Raphael Greifenstein, Dhana Röhrs, Tim Ballweg, Juliana Pfeifer, Eric Gottwald, Masanari Takamiya, Matthias Franzreb, Christof Wöll
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引用次数: 0

摘要

将生物催化剂整合到金属有机框架(MOFs)中具有增强生物催化剂稳定性和维持生物催化剂在有机溶剂中活性的潜力,因此正引起越来越多的关注。然而,促进此类大分子合成后渗入 MOF 孔隙的因素仍不清楚。通过这项系统性研究,我们确定了生物催化剂的分子大小、分子量和亲和力对典型 MOF NU-1000 吸收的影响。我们分析了分子量从 1.9 kDa 到 44.4 kDa 的六种生物催化剂。通过结合使用荧光标记和 3D-STED 激光共聚焦扫描显微镜,我们区分了内置于 MOF 孔中的生物催化剂和被立体排斥的生物催化剂。我们对寄存在 MOF 中的生物催化剂的催化功能进行了研究,发现与溶解的情况相比,它们的催化功能有很大的变化,从增加两倍到大幅降低不等。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Integrating Biocatalysts into Metal-Organic Frameworks: Disentangling the Roles of Affinity, Molecular Weight, and Size.

The integration of biocatalysts within metal-organic frameworks (MOFs) is attracting growing interest due to its potential to both enhance biocatalyst stability and sustain biocatalyst activity in organic solvents. However, the factors that facilitate the post-synthetic infiltration of such large molecules into MOF pores remain unclear. This systematic study enabled the identification of the influence of biocatalyst molecular size, molecular weight and affinity on the uptake by an archetypal MOF, NU-1000. We analyzed a range of six biocatalysts with molecular weights from 1.9 kDa to 44.4 kDa, respectively. By employing a combination of fluorescence tagging and 3D-STED confocal laser scanning microscopy, we distinguished between biocatalysts that were internalized within the MOF pores and those sterically excluded. The catalytic functions of the biocatalysts hosted within the MOF were investigated and found to show strong variations relative to the solvated case, ranging from a two-fold increase to a strong decrease.

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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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