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Ries, J.* ; Bayer, M.* ; Csúcs, G.* ; Dirkx, R.* ; Solimena, M.* ; Ewers, H.* ; Schwille, P.*

Automated suppression of sample-related artifacts in Fluorescence Correlation Spectroscopy.

Opt. Express. 18, 11073-11082 (2010)
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Open Access Gold möglich sobald Verlagsversion bei der ZB eingereicht worden ist.
Fluorescence Correlation Spectroscopy (FCS) in cells often suffers from artifacts caused by bright aggregates or vesicles, depletion of fluorophores or bleaching of a fluorescent background. The common practice of manually discarding distorted curves is time consuming and subjective. Here we demonstrate the feasibility of automated FCS data analysis with efficient rejection of corrupted parts of the signal. As test systems we use a solution of fluorescent molecules, contaminated with bright fluorescent beads, as well as cells expressing a fluorescent protein (ICA512-EGFP), which partitions into bright secretory granules. This approach improves the accuracy of FCS measurements in biological samples, extends its applicability to especially challenging systems and greatly simplifies and accelerates the data analysis.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
ISSN (print) / ISBN 1094-4087
e-ISSN 1094-4087
Zeitschrift Optics Express
Quellenangaben Band: 18, Heft: 11, Seiten: 11073-11082 Artikelnummer: , Supplement: ,
Verlag Optical Society of America (OSA)
Begutachtungsstatus Peer reviewed
Institut(e) Institute for Pancreatic Beta Cell Research (IPI)