| Literature DB >> 26123183 |
Yong Wu1, Xundong Wu2, Ligia Toro3, Enrico Stefani4.
Abstract
STED (stimulated emission depletion) is a popular super-resolution fluorescence microscopy technique. In this paper, we present a concise guide to building a resonant-scanning STED microscope with ultrafast photon-counting acquisition. The STED microscope has two channels, using a pulsed laser and a continuous-wave (CW) laser as the depletion laser source, respectively. The CW STED channel preforms time-gated detection to enhance optical resolution in this channel. We use a resonant mirror to attain high scanning speed and ultrafast photon counting acquisition to scan a large field of view, which help reduce photobleaching. We discuss some practical issues in building a STED microscope, including creating a hollow depletion beam profile, manipulating polarization, and monitoring optical aberration. We also demonstrate a STED image enhancement method using stationary wavelet expansion and image analysis methods to register objects and to quantify colocalization in STED microscopy.Entities:
Keywords: Colocalization; Fluorescence microscopy; Image analysis; Resonant scanning; STED microscopy
Mesh:
Year: 2015 PMID: 26123183 PMCID: PMC4630089 DOI: 10.1016/j.ymeth.2015.06.019
Source DB: PubMed Journal: Methods ISSN: 1046-2023 Impact factor: 3.608