勃姆石
化学
亨廷顿蛋白
抗氧化剂
亨廷顿病
生物化学
包裹体(矿物)
突变体
生物物理学
有机化学
疾病
矿物学
生物
内科学
铝
医学
基因
作者
Álvaro Martínez‐Camarena,Marián Merino,Ana Virginia Sánchez-Sánchez,Salvador Blasco,José M. Llinares,José L. Mullor,Enrique García‐España
摘要
A novel amino-nanozyme, based on boehmite nanoparticles (BNPs) functionalised with a tetra-azapyridinophane (L1), has been designed to undermine some of the key issues underlying Huntington disease. L1 forms Cu2+ complexes with a striking SOD activity, while when grafted to the BNPs displays mitoROS scavenging properties and ability to disaggregate mutant huntingtin deposits in cells.
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