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一种锰氧化物纳米酶可以防止生物分子的氧化损伤,而不影响内源性抗氧化系统。

A manganese oxide nanozyme prevents the oxidative damage of biomolecules without affecting the endogenous antioxidant system.

机构信息

Department of Inorganic and Physical Chemistry, Indian Institute of Science, Bangalore 560012, India.

出版信息

Nanoscale. 2019 Feb 28;11(9):3855-3863. doi: 10.1039/c8nr09397k.

Abstract

Biocompatible nanoparticles with an intrinsic ability to mimic the cellular antioxidant enzymes are potential candidates for the development of new therapeutics for various oxidative stress related disorders. However, the understanding of the interaction and the mechanistic crosstalk between the nanoparticles and the cellular biomolecules is limited. Here we show that the multienzyme mimic manganese(ii,iii) oxide, Mn3O4, in nanoform (Mp) rescues the cells from oxidative damage induced by reactive oxygen species (ROS). The nanoparticles provide remarkable protection to biomolecules against the ROS-mediated protein oxidation, lipid peroxidation and DNA damage. Interestingly, the endogenous antioxidant machinery remains unaltered in the presence of these nanozymes, indicating the small molecule targeting of these nanoparticles in the cellular redox modulation. This study delineates the possible mechanism by which the nanoparticles provide protection to the cells against the adverse effects of oxidative stress. Based on our observation, we suggest that the multienzyme mimic Mn3O4 nanoparticles possess great potential in suppressing the oxidative stress-mediated pathophysiological conditions under which the antioxidant system is overwhelmed.

摘要

具有模拟细胞抗氧化酶固有能力的生物相容性纳米粒子是开发用于各种与氧化应激相关疾病的新型治疗方法的潜在候选物。然而,纳米粒子与细胞生物分子之间的相互作用和机制串扰的理解有限。在这里,我们表明,多酶模拟的二氧化锰(Mn3O4)纳米形式(Mp)可以挽救细胞免受活性氧(ROS)诱导的氧化损伤。这些纳米粒子为生物分子提供了对 ROS 介导的蛋白质氧化、脂质过氧化和 DNA 损伤的显著保护。有趣的是,在存在这些纳米酶的情况下,内源性抗氧化机制保持不变,表明这些纳米粒子在细胞氧化还原调节中靶向小分子。本研究阐明了纳米粒子为细胞提供针对氧化应激不利影响的保护的可能机制。基于我们的观察,我们建议多酶模拟 Mn3O4 纳米粒子具有在抑制抗氧化系统不堪重负的氧化应激介导的病理生理条件下抑制氧化应激的巨大潜力。

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