生物正交化学
纳米反应器
催化作用
材料科学
叠氮化物
组合化学
过渡金属
前药
微型反应器
纳米技术
介孔材料
化学
点击化学
有机化学
生物化学
作者
Zhiguo Gao,Yaojia Li,Jiaqi Xing,Yougong Lu,Quanlin Shao,Jinzhong Hu,Shan Zhao,Wei He,Bai‐Wang Sun
标识
DOI:10.1021/acsami.3c19133
摘要
Employing transition metal catalysts (TMCs) to perform bioorthogonal activation of prodrugs and pro-fluorophores in biological systems, particularly in a conditional fashion, remains a challenge. Here, we used a mesoporous organosilica nanoscaffold (RuMSN), which localizes Ru(II) conjugates on the pore wall, enabling the biorthogonal photoreduction reactions of azide groups. Due to easily adjustable surface charges and pore diameter, this efficiently engineering RuMSN catalyst, with abundant active sites on the inner pore well, could spontaneously repel or attract substrates with different molecular sizes and charges and thus ensure selective bioorthogonal catalysis. Depending on it, engineering RuMSN nanoreactors showed fascinating application scales from conditional bioorthogonal activation of prodrugs and pro-fluorophores in either intra- or extracellular localization to performing intracellular concurrent and tandem catalysis together with natural enzymes.
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