journal article·2020-07-24

Oxidized Activated Charcoal Nanoparticles as Catalytic Superoxide Dismutase Mimetics: Evidence for Direct Participation of an Intrinsic Radical

Gang Wu, Emily A. McHugh, Vladimir Berka, Weiyin Chen, Zhe Wang, Jacob L. Beckham, Paul J. Derry, Trenton Roy, Thomas A. Kent, James M. Tour, Ah-Lim Tsai

ACS Applied Nano Materials· Volume 3· Issue 7
Publisher page

Abstract

The mechanism for carbon-based superoxide dismutase (SOD) nanomimetics is not known, hindering the optimization of this potentially clinically useful feature. Here we studied oxidized activated charcoal (OAC) prepared by fuming nitric acid oxidation of activated charcoal and characterized its properties. The OAC nanoparticles have sizes 5–30 nm and are highly water-soluble. The OACs are strong SOD mimetics with a kcat = 2.1 × 105 s–1 at pH 12.7 and ∼108 M–1 s–1 rate constants at pH 8.5, having great potential in therapeutic application for disorders with pathological superoxide levels. Electron paramagnetic resonance (EPR) indicates that resting OACs are fully oxidized, exhibiting a stoichiometric level of an intrinsic radical. The OACs can be reduced with superoxide, leading to a decreased level of the intrinsic radical; however, the reduction is incomplete even at high superoxide levels. This outcome was predicted by a simple two-step SOD reaction mechanism using the species containing the intrinsic radical as the fully oxidized state. Pretreatment of the OACs with superoxide causes little change to its SOD activity, indicating that a stoichiometric amount of the intrinsic radical is not mandatory for full activity. This study indicates the direct participation of the intrinsic radical in the catalytic turnover of a highly active SOD-like nanozyme.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Advanced Nanomaterials in Catalysis · Electrochemical sensors and biosensors · Carbon and Quantum Dots Applications

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Division of Hematology, Department of Internal Medicine, McGovern Medical School—University of Texas, 6431 Fannin Street, Houston, Texas 77030, United States

Center for Translational Research in Inflammatory Diseases, Michael E. DeBakey VA Medical Center, 2002 Holcombe Boulevard, Houston, Texas 77030, United States

Institute of Biosciences and Technology, Texas A&M Health Science Center, 2121 West Holcombe Boulevard, Houston, Texas 77030, United States

Stanley H. Appel Department of Neurology, Houston Methodist Hospital and Research Institute, 6560 Fannin Street, Houston, Texas 77030, United States

Funding

National Institute of Neurological Disorders and Stroke · Welch Foundation

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