Single-Molecule Flow Platform for the Quantification of Biomolecules Attached to Single Nanoparticles

被引:8
|
作者
Jung, Seung-Ryoung [1 ]
Han, Rui [1 ]
Sun, Wei [1 ,2 ]
Jiang, Yifei [1 ]
Fujimoto, Bryant S. [1 ]
Yu, Jiangbo [1 ]
Kuo, Chun-Ting [1 ]
Rong, Yu [1 ]
Zhou, Xing-Hua [1 ]
Chiu, Daniel T. [1 ]
机构
[1] Univ Washington, Dept Chem, Seattle, WA 98195 USA
[2] Corning Inc, Corning, NY 14830 USA
关键词
SEMICONDUCTING POLYMER DOTS; CONFOCAL CORRELATION SPECTROSCOPY; GOLD NANOPARTICLES; QUANTITATIVE MICROSCOPY; SENSITIVITY; MEDICINE; ULTRABRIGHT; SCATTERING; PROTEINS; BIOLOGY;
D O I
10.1021/acs.analchem.8b00024
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
We describe here a flow platform for quantifying the number of biomolecules on individual fluorescent nanoparticles. The platform combines line-confocal fluorescence detection with near nanoscale channels (1-2 mu m in width and height) to achieve high single-molecule detection sensitivity and throughput. The number of biomolecules present on each nanoparticle was determined by deconvolving the fluorescence intensity distribution of single-nanoparticle biomolecule complexes with the intensity distribution of single biomolecules. We demonstrate this approach by quantifying the number of streptavidins on individual semiconducting polymer dots (Pdots); streptavidin was rendered fluorescent using biotin-Alexa647. This flow platform has high-throughput (hundreds to thousands of nanoparticles detected per second) and requires minute amounts of sample (similar to 5 mu L at a dilute concentration of 10 pM). This measurement method is an additional tool for characterizing synthetic or biological nanoparticles.
引用
收藏
页码:6089 / 6095
页数:7
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