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Updated: Jan 14, 2026

Three-dimensional Super Resolution Microscopy of F-actin Filaments by Interferometric PhotoActivated Localization Microscopy iPALM
Published on: December 1, 2016
Real-time, high-throughput super-resolution microscopy via panoramic integration
Kyungduck Yoon1,2,3,4, Hansol Yoon1,2,5, Kidan Tadesse1,2,3
1Laboratory for Systems Biophotonics, Georgia Institute of Technology, Atlanta, GA, USA.
Abstract:
We introduce super-resolution panoramic integration (SPI), an on-the-fly microscopy technique enabling instantaneous generation of subdiffractional images concurrently with scalable, high-throughput screening. SPI leverages multifocal optical rescaling, high-content sweeping, and synchronized line-scan readout while preserving minimal post-processing and compatibility with epi-fluorescence settings. We demonstrate SPI for various subcellular and populational morphology, function, and heterogeneity. This versatile platform offers a practical pathway toward biological insights beyond traditional optical and computational constraints.

