分辨率(逻辑)
细胞骨架
超分辨率
显微镜
时间分辨率
内吞作用
活体细胞成像
计算机科学
光学
内吞循环
化学
物理
生物系统
细胞
人工智能
图像(数学)
生物
生物化学
作者
Dong Li,Lin Shao,Bi‐Chang Chen,Xi Zhang,Mingshu Zhang,Brian T. Moses,Daniel E. Milkie,Jordan R. Beach,John A. Hammer,Mithun Pasham,Tomas Kirchhausen,Michelle A. Baird,Michael W. Davidson,Pingyong Xu,Eric Betzig
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2015-08-27
卷期号:349 (6251)
被引量:698
标识
DOI:10.1126/science.aab3500
摘要
Adding to the super-resolution arsenal Structured illumination microscopy (SIM) uses light intensities that are orders of magnitude lower than other super-resolution methods. SIM is also far faster over cellular-sized fields of view. Li et al. used two approaches to improve the resolution of SIM to allow live cell imaging of dynamic cellular processes, including endocytosis and cytoskeleton remodeling. The contrast in performance between SIM and other techniques is due to a few key differences. Defining the practical resolution at the limited signal-to-noise ratios necessary for live cell imaging will require better imaging metrics. Science , this issue 10.1126/science.aab3500
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