显微镜
分辨率(逻辑)
原位
DNA
纳米尺度
超分辨显微术
超分辨率
纳米结构
分子
生物物理学
纳米技术
化学
生物系统
材料科学
计算机科学
物理
生物
光学
人工智能
图像(数学)
生物化学
有机化学
扫描共焦电子显微镜
作者
Ralf Jungmann,Mauricio Avendaño,Mingjie Dai,Johannes B. Woehrstein,Sarit S. Agasti,Zachary Feiger,Avital A. Rodal,Peng Yin
出处
期刊:Nature Methods
[Nature Portfolio]
日期:2016-03-28
卷期号:13 (5): 439-442
被引量:369
摘要
Counting molecules in complexes is challenging, even with super-resolution microscopy. Here, we use the programmable and specific binding of dye-labeled DNA probes to count integer numbers of targets. This method, called quantitative points accumulation in nanoscale topography (qPAINT), works independently of dye photophysics for robust counting with high precision and accuracy over a wide dynamic range. qPAINT was benchmarked on DNA nanostructures and demonstrated for cellular applications by quantifying proteins in situ and the number of single-molecule FISH probes bound to an mRNA target.
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