分子生物学
IVD分子诊断
细胞培养与分析
蛋白研究
细胞因子
重组蛋白
抗体
高通量测序建库
病原检测UCF系列
生物医药
工具酶
抑制剂激活剂与常用试剂
仪器
耗材

Engineering catalytic dephosphorylation reaction for endotoxin inactivation

Meng Gao, Xi Liu, Zhenzhen Wang, Hui Wang, Tristan Asset, Di Wu, Jun Jiang, Qianqian Xie, Shujuan Xu, Xiaoming Cai, Jia Li, Weili Wang, Huizhen Zheng, Xingfa Gao, Nikolai Tarasenko, Benjamin Rotonnel

Journal:Nano Today

IF:18.96

DOI:10.1016/j.nantod.2022.101456

PMID:

Published:2022-03-14

research field:神经科学药理学细胞生物学

Abstract

Although lives have been saved due to the discovery of endotoxin removal methods including solvent extraction and affinity adsorption, they have limitations in treatment capacity, efficiency or costs. Endotoxin contaminations still result in a large number of deaths in global every year. This necessitates a mechanistic breakthrough for endotoxin removal or inactivation. Herein, we engineered a dephosphorylation reaction on endotoxins by a synthetic nanozyme (CeO 2 ) to attenuate the toxicity. CeO 2 prepared in phosphate-free hydrothermal reaction selectively and efficiently catalyzed the breaking of P-O bonds in endotoxins. Catalytic depletion of phosphates from endotoxins attenuated their binding with Toll-like receptors, NF-κB activation and pro-inflammatory cytokine release. Airborne LPS was, for the first time, inactivated (98%) by this facile dephosphorylation reaction. A CeO 2 integrating column displayed a 16-fold higher treatment capacity than commercial resins to aqueous endotoxins (water and protein solution). Overall, our findings offer a different mechanistic insight for removal of endotoxins.

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