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Vacancy-Engineered Nanoceria: Enzyme Mimetic Hotspots for the Degradation of Nerve Agents

Organophosphorus‐based nerve agents, such as paraoxon, parathion, and malathion, inhibit acetylcholinesterase, which results in paralysis, respiratory failure, and death. Bacteria are known to use the enzyme phosphotriesterase (PTE) to break down these compounds. In this work, we designed vacancy‐en...

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Bibliographic Details
Published in:Angewandte Chemie International Edition 2016-01, Vol.55 (4), p.1412-1416
Main Authors: Vernekar, Amit A., Das, Tandrila, Mugesh, Govindasamy
Format: Article
Language:English
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Summary:Organophosphorus‐based nerve agents, such as paraoxon, parathion, and malathion, inhibit acetylcholinesterase, which results in paralysis, respiratory failure, and death. Bacteria are known to use the enzyme phosphotriesterase (PTE) to break down these compounds. In this work, we designed vacancy‐engineered nanoceria (VE CeO2 NPs) as PTE mimetic hotspots for the rapid degradation of nerve agents. We observed that the hydrolytic effect of the nanomaterial is due to the synergistic activity between both Ce3+ and Ce4+ ions located in the active site‐like hotspots. Furthermore, the catalysis by nanoceria overcomes the product inhibition generally observed for PTE and small molecule‐based PTE mimetics. Catalytic hotspots: Vacancy‐engineered cerium dioxide nanoparticles provide potential enzyme mimetic hotspots for the rapid degradation of nerve agents. This study presents the first example of hydrolytic activity of a vacancy‐engineered nanomaterial, where the dual oxidation states of the metal ions play a crucial role.
ISSN:1433-7851
1521-3773
DOI:10.1002/anie.201510355