超分子化学
生物催化
甲酸
化学
堆积
组合化学
选择性
芘
材料科学
溶剂
催化作用
纳米技术
有机化学
离子液体
晶体结构
作者
Wei Huang,Haitao Yuan,Hongling Yang,Xiaomin Ma,Shuyao Huang,Hongjie Zhang,Siming Huang,Guosheng Chen,Gangfeng Ouyang
标识
DOI:10.1038/s41467-023-39364-x
摘要
Abstract Rational integration of native enzymes and nanoscaffold is an efficient means to access robust biocatalyst, yet remains on-going challenges due to the trade-off between fragile enzymes and harsh assembling conditions. Here, we report a supramolecular strategy enabling the in situ fusion of fragile enzymes into a robust porous crystal. A c2-symmetric pyrene tecton with four formic acid arms is utilized as the building block to engineer this hybrid biocatalyst. The decorated formic acid arms afford the pyrene tectons high dispersibility in minute amount of organic solvent, and permit the hydrogen-bonded linkage of discrete pyrene tectons to an extended supramolecular network around an enzyme in almost organic solvent-free aqueous solution. This hybrid biocatalyst is covered by long-range ordered pore channels, which can serve as the gating to sieve the catalytic substrate and thus enhance the biocatalytic selectivity. Given the structural integration, a supramolecular biocatalyst-based electrochemical immunosensor is developed, enabling the pg/mL detection of cancer biomarker.
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