2024/07/10 by Hanzhe Wu, Danni Chen, Wu, Hanzhe +9
Engineering · #Advanced MEMS and NEMS Technologies #Biological Physics (physics.bio-ph) #CCD and CMOS Imaging Sensors #FOS: Physical sciences #Optics (physics.optics) #Photonic and Optical Devices
paper · pdf · doi:10.48550/arxiv.2407.07681
openalex publication_date 2024/07/10 · openalex created_date 2024/07/13 · openalex updated_date 2026/07/28
Among the approaches in three-dimensional (3D) single molecule localization microscopy, there are several point spread function (PSF) engineering approaches, in which depth information of molecules is encoded in 2D images. Usually,the molecules are excited sparsely in each raw image. The consequence is that the temporal resolution has to be sacrificed. In order to improve temporal resolution and ensure localization accuracy, we propose a method, SH-CS, based on light needle excitation, detection system with single helix-point spread function (SH-PSF), and compressed sensing (CS). Although the SH-CS method still has a limitation about the molecule density, it is suited for relatively dense molecules. For each light needle scanning position, an SH image of excited molecules is processed with CS algorithm to decode their axial information. Simulations demonstrated, for random distributed 1 ~ 15 molecules in depth range of 4 μm, the axial localization accuracy is 12.1 nm ~ 73.5 nm. The feasibility of this method is validated by experimental data.