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Molecular Crowding and a Minimal Footprint at a Gold Nanoparticle Support Stabilize Glucose Oxidase and Boost its Activity

submitted on 12.12.2019, 15:17 and posted on 18.12.2019, 12:52 by Yuanmo Wang, Rima Jonkute, Hampus Lindmark, Jacqueline D. Keighron, Ann-Sofie Cans
Enzymes conjugated to nanomaterials are used in the design of various biotechnologies. In development of biosensors, surface modifications with the enzyme glucose oxidase (GOx) serve to aid the detection of blood glucose. In order to optimize sensor effectiveness, the enzyme tertiary structure needs to be preserved upon immobilization to retain the enzyme´s catalytic activity. Due to the nature of GOx, it suffers from tendency to denature when immobilized at a solid surface, methods to optimize enzyme stability are of great importance. Here, we introduce the study of the interaction of GOx to the highly curved surface of 20 nm gold nanoparticles (AuNP) that shows how placing a monolayer of enzyme where the enzyme spreads thin at the AuNP surface still provides stable catalytic performance up to14 days compared to enzymes free in solution. Moreover, by increasing enzyme density and creating a molecularly crowded environment at the highly curved nanoparticle surface, which limits the size of the enzyme footprint for attachment, the activity per enzyme can be enhanced up to 300%. This is of great importance for implementing stable and sensitive sensor technologies that are constructed by enzyme-based nanoparticle scaffolds. Here, we show by using the conditions that maintain GOx structure and function when limiting the enzyme coating to an ultra-thin layer, the design and construction of ultrafast responding diagnostic sensor technology for glucose can be achieved, which is crucial for monitoring rapid fluctuations of for instance, glucose in the brain.


The Swedish Research Council and The Chalmers Areas of Advance Nanoscience and Nanotechnology


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Chalmers University of Technology



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Declaration of Conflict of Interest

The authors declare no conflict of interest.