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Photon counting imaging and centroiding with an electron-bombarded CCD using single molecule localisation software

Photon event centroiding in photon counting imaging and single-molecule localisation in super-resolution fluorescence microscopy share many traits. Although photon event centroiding has traditionally been performed with simple single-iteration algorithms, we recently reported that iterative fitting...

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Detalles Bibliográficos
Autores principales: Hirvonen, Liisa M., Barber, Matthew J., Suhling, Klaus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier B.V 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4825609/
https://www.ncbi.nlm.nih.gov/pubmed/27274604
http://dx.doi.org/10.1016/j.nima.2016.03.024
Descripción
Sumario:Photon event centroiding in photon counting imaging and single-molecule localisation in super-resolution fluorescence microscopy share many traits. Although photon event centroiding has traditionally been performed with simple single-iteration algorithms, we recently reported that iterative fitting algorithms originally developed for single-molecule localisation fluorescence microscopy work very well when applied to centroiding photon events imaged with an MCP-intensified CMOS camera. Here, we have applied these algorithms for centroiding of photon events from an electron-bombarded CCD (EBCCD). We find that centroiding algorithms based on iterative fitting of the photon events yield excellent results and allow fitting of overlapping photon events, a feature not reported before and an important aspect to facilitate an increased count rate and shorter acquisition times.