Literature DB >> 20588915

Single plane illumination fluorescence correlation spectroscopy (SPIM-FCS) probes inhomogeneous three-dimensional environments.

Thorsten Wohland1, Xianke Shi, Jagadish Sankaran, Ernst H K Stelzer.   

Abstract

The life sciences require new highly sensitive imaging tools, which allow the quantitative measurement of molecular parameters within a physiological three-dimensional (3D) environment. Therefore, we combined single plane illumination microscopy (SPIM) with camera based fluorescence correlation spectroscopy (FCS). SPIM-FCS provides contiguous particle number and diffusion coefficient images with a high spatial resolution in homo- and heterogeneous 3D specimens and live zebrafish embryos. Our SPIM-FCS recorded up to 4096 spectra within 56 seconds at a laser power of 60 microW without damaging the embryo. This new FCS modality provides more measurements per time and more, less photo-toxic measurements per sample than confocal based methods. In essence, SPIM-FCS offers new opportunities to observe biomolecular interactions quantitatively and functions in a highly multiplexed manner within a physiologically relevant 3D environment. (c) 2010 Optical Society of America.

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Year:  2010        PMID: 20588915     DOI: 10.1364/OE.18.010627

Source DB:  PubMed          Journal:  Opt Express        ISSN: 1094-4087            Impact factor:   3.894


  46 in total

1.  Development of time-integrated multipoint moment analysis for spatially resolved fluctuation spectroscopy with high time resolution.

Authors:  Doogie Oh; Alexandra Zidovska; Yangqing Xu; Daniel J Needleman
Journal:  Biophys J       Date:  2011-09-20       Impact factor: 4.033

2.  Dissecting chromatin interactions in living cells from protein mobility maps.

Authors:  Fabian Erdel; Katharina Müller-Ott; Michael Baum; Malte Wachsmuth; Karsten Rippe
Journal:  Chromosome Res       Date:  2011-01       Impact factor: 5.239

3.  Imaging fluorescence (cross-) correlation spectroscopy in live cells and organisms.

Authors:  Jan W Krieger; Anand P Singh; Nirmalya Bag; Christoph S Garbe; Timothy E Saunders; Jörg Langowski; Thorsten Wohland
Journal:  Nat Protoc       Date:  2015-11-05       Impact factor: 13.491

4.  Quantitative fluorescence imaging of protein diffusion and interaction in living cells.

Authors:  Jérémie Capoulade; Malte Wachsmuth; Lars Hufnagel; Michael Knop
Journal:  Nat Biotechnol       Date:  2011-08-07       Impact factor: 54.908

5.  Exploring the dynamics of cell processes through simulations of fluorescence microscopy experiments.

Authors:  Juan Angiolini; Nicolas Plachta; Esteban Mocskos; Valeria Levi
Journal:  Biophys J       Date:  2015-06-02       Impact factor: 4.033

6.  Light-sheet fluorescence microscopy for quantitative biology.

Authors:  Ernst H K Stelzer
Journal:  Nat Methods       Date:  2015-01       Impact factor: 28.547

7.  Imaging stress.

Authors:  Shlomi Brielle; Rotem Gura; Daniel Kaganovich
Journal:  Cell Stress Chaperones       Date:  2015-07-04       Impact factor: 3.667

8.  Quantifying transcription factor-DNA binding in single cells in vivo with photoactivatable fluorescence correlation spectroscopy.

Authors:  Ziqing Winston Zhao; Melanie D White; Yanina D Alvarez; Jennifer Zenker; Stephanie Bissiere; Nicolas Plachta
Journal:  Nat Protoc       Date:  2017-06-29       Impact factor: 13.491

9.  Widefield High Frame Rate Single-Photon SPAD Imagers for SPIM-FCS.

Authors:  Jan Buchholz; Jan Krieger; Claudio Bruschini; Samuel Burri; Andrei Ardelean; Edoardo Charbon; Jörg Langowski
Journal:  Biophys J       Date:  2018-05-10       Impact factor: 4.033

10.  Random Motion of Chromatin Is Influenced by Lamin A Interconnections.

Authors:  Fereydoon Taheri; Buse Isbilir; Gabriele Müller; Jan W Krieger; Giuseppe Chirico; Jörg Langowski; Katalin Tóth
Journal:  Biophys J       Date:  2018-05-11       Impact factor: 4.033

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