| Literature DB >> 29600995 |
Cheng Zheng, Guangyuan Zhao, Wenjie Liu, Youhua Chen, Zhimin Zhang, Luhong Jin, Yingke Xu, Cuifang Kuang, Xu Liu.
Abstract
Measuring three-dimensional nanoscale cellular structures is challenging, especially when the structure is dynamic. Owing to the informative total internal reflection fluorescence (TIRF) imaging under varied illumination angles, multi-angle (MA) TIRF has been examined to offer a nanoscale axial and a subsecond temporal resolution. However, conventional MA-TIRF still performs badly in lateral resolution and fails to characterize the depth image in densely distributed regions. Here, we emphasize the lateral super-resolution in the MA-TIRF, exampled by simply introducing polarization modulation into the illumination procedure. Equipped with a sparsity and accelerated proximal algorithm, we examine a more precise 3D sample structure compared with previous methods, enabling live cell imaging with a temporal resolution of 2 s and recovering high-resolution mitochondria fission and fusion processes. We also shared the recovery program, which is the first open-source recovery code for MA-TIRF, to the best of our knowledge.Mesh:
Substances:
Year: 2018 PMID: 29600995 DOI: 10.1364/OL.43.001423
Source DB: PubMed Journal: Opt Lett ISSN: 0146-9592 Impact factor: 3.776