超分辨率
菁
显微镜
光激活定位显微镜
超分辨显微术
分辨率(逻辑)
纳米技术
时间分辨率
荧光寿命成像显微镜
材料科学
图像分辨率
荧光显微镜
跟踪(教育)
荧光
生物系统
光学
物理
计算机科学
生物
人工智能
图像(数学)
心理学
教育学
作者
George H. Patterson,Michael W. Davidson,Suliana Manley,Jennifer Lippincott‐Schwartz
标识
DOI:10.1146/annurev.physchem.012809.103444
摘要
Superresolution imaging is a rapidly emerging new field of microscopy that dramatically improves the spatial resolution of light microscopy by over an order of magnitude (∼10–20-nm resolution), allowing biological processes to be described at the molecular scale. Here, we discuss a form of superresolution microscopy based on the controlled activation and sampling of sparse subsets of photoconvertible fluorescent molecules. In this single-molecule-based imaging approach, a wide variety of probes have proved valuable, ranging from genetically encodable photoactivatable fluorescent proteins to photoswitchable cyanine dyes. These have been used in diverse applications of superresolution imaging: from three-dimensional, multicolor molecule localization to tracking of nanometric structures and molecules in living cells. Single-molecule-based superresolution imaging thus offers exciting possibilities for obtaining molecular-scale information on biological events occurring at variable timescales.
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