Nanoconfinement-Enhanced Electrochemiluminescence for in Situ Imaging of Single Biomolecules

被引:59
|
作者
Lu, Yanwei [1 ,2 ]
Huang, Xuedong [1 ,2 ]
Wang, Shurong [1 ,2 ]
Li, Binxiao [1 ,2 ]
Liu, Baohong [1 ,2 ]
机构
[1] Fudan Univ, Shanghai Stomatol Hosp, Dept Chem, State Key Lab Mol Engn Polymers, Shanghai 200433, Peoples R China
[2] Fudan Univ, Inst Biomed Sci, Shanghai 200433, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划; 中国博士后科学基金;
关键词
electrochemiluminescence; nanoreactor; nanoconfinement-enhanced emission; single-molecule imaging; dual-signal imaging mode;
D O I
10.1021/acsnano.2c11934
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Direct imaging of electrochemical reactions at the single-molecule level is of potential interest in materials, diagnostic, and catalysis applications. Electrochemiluminescence (ECL) offers the opportunity to convert redox events into photons. However, it is challenging to capture single photons emitted from a single-molecule ECL reaction at a specific location, thus limiting high-quality imaging applications. We developed the nanoreactors based on Ru(bpy)32+-doped nanoporous zeolite nanoparticles (Ru@zeolite) for direct visualization of nanoconfinement-enhanced ECL reactions. Each nanoreactor not only acts as a matrix to host Ru(bpy)32+ molecules but also provides a nanoconfined environment for the collision reactions of Ru(bpy)32+ and co-reactant radicals to realize efficient in situ ECL reactions. The nanoscale confinement resulted in enhanced ECL. Using such nanoreactors as ECL probes, a dual-signal sensing protocol for visual tracking of a single biomolecule was performed. High-resolution imaging of single membrane proteins on heterogeneous cells was effectively addressed with near-zero backgrounds. This could provide a more sensitive tool for imaging individual biomolecules and significantly advance ECL imaging in biological applications.
引用
收藏
页码:3809 / 3817
页数:9
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