Size-Selective Capturing of Exosomes Using DNA Tripods

被引:6
|
作者
Iinuma, Ryosuke [1 ,2 ]
Chen, Xiaoxia [3 ]
Masubuchi, Takeya [1 ,4 ]
Ueda, Takuya [1 ,5 ]
Tadakuma, Hisashi [1 ,3 ,6 ]
机构
[1] Univ Tokyo, Grad Sch Frontier Sci, Chiba 2778562, Japan
[2] JSR Corp, Tsukuba, Ibaraki 3050841, Japan
[3] ShanghaiTech Univ, Sch Life Sci & Technol, Shanghai 201210, Peoples R China
[4] Univ Calif San Diego, Sch Biol Sci, Dept Cell & Dev Biol, La Jolla, CA 92093 USA
[5] Waseda Univ, Grad Sch Sci & Engn, Tokyo 1628480, Japan
[6] ShanghaiTech Univ, Gene Editing Ctr, Sch Life Sci & Technol, Shanghai 201210, Peoples R China
基金
日本学术振兴会; 中国国家自然科学基金;
关键词
EXTRACELLULAR VESICLES; NANOSTRUCTURES; DECORATION; DISTANCE;
D O I
10.1021/jacs.3c11067
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Fractionating and characterizing target samples are fundamental to the analysis of biomolecules. Extracellular vesicles (EVs), containing information regarding the cellular birthplace, are promising targets for biology and medicine. However, the requirement for multiple-step purification in conventional methods hinders analysis of small samples. Here, we apply a DNA origami tripod with a defined aperture of binders (e.g., antibodies against EV biomarkers), which allows us to capture the target molecule. Using exosomes as a model, we show that our tripod nanodevice can capture a specific size range of EVs with cognate biomarkers from a broad distribution of crude EV mixtures. We further demonstrate that the size of captured EVs can be controlled by changing the aperture of the tripods. This simultaneous selection with the size and biomarker approach should simplify the EV purification process and contribute to the precise analysis of target biomolecules from small samples.
引用
收藏
页码:10293 / 10298
页数:6
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