化学
纳米技术
生物催化
生物传感器
纳米材料
纳米反应器
介孔材料
荧光
生物界面
整体
点击化学
纳米颗粒
分子工程
固定化酶
量子点
生物物理学
可重用性
微型多孔材料
纳米载体
合理设计
生物相容性材料
组合化学
原位
石墨烯
作者
Yuechun Li,Chenjie Nie,Chunyan Ji,Zhaowen Cui,Yanwei Ji,Min Ma,Wentao Zhang,Leina Dou,Qianjin Liu,Jianlong Wang
标识
DOI:10.1021/acs.analchem.5c03889
摘要
Harmonizing enzyme-support microenvironments to govern thermodynamic interaction landscapes presents a critical yet underexplored frontier in nanobiocatalysis for pathogen detection. Herein, we architecturally engineer mesoporous resorcinol formaldehyde nanospheres (mRFNSs, 9.95 nm pores) with tailored surface chemistry to elucidate how microenvironment modulation dictates enzyme immobilization energetics. Thermodynamic dissection demonstrates that betaine-tailored mRFNSs with optimal immobilization efficiency and activity dramatically reshape binding energetics, achieving record affinity through optimized electrostatic complementarity, hydrogen-bond networks, and hydrophobic effect. This microenvironment engineering strategy delivers an unprecedented 4.01-fold enhancement in binding constant ( K a = 1.12 × 10 8 vs 2.79 × 10 7 M –1 ) and superior thermodynamic spontaneity (Δ G = −46.0 vs −42.5 kJ mol –1 ). Leveraging this, we develop a paradigm-shifting ratiometric fluorescence immunoassay where ALP triggers in situ silicon quantum dot (SiQDs) synthesis (530 nm) against tetraphenylbenzidine reference (620 nm), achieving ultrasensitive Salmonella typhimurium ( S. typhimurium ) detection (100 CFU mL –1 ), which is 50-fold lower than that of conventional ELISA. A convolutional neural network (CNN) decodes smartphone-captured fluorescence hues, enabling portable classification (93.75% accuracy) of pathogen levels. Validated in food matrices (81.44–116.93% recovery), this work establishes thermodynamic-microenvironment correlations as a blueprint for next-generation nanobiocatalysts, bridging biointerface science with artificial intelligence (AI)-enhanced diagnostics.
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