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Protein Diffusion in Mammalian Cell Cytoplasm
by
Dross, Nicolas
, Willman, Sami F.
, Kühn, Thomas
, Langowski, Jörg
, Vihinen-Ranta, Maija
, Ihalainen, Teemu O.
, Hyväluoma, Jari
, Timonen, Jussi
in
Animals
/ Bacterial Proteins - metabolism
/ Binding sites
/ Biology
/ Biophysics
/ Cats
/ Cell lines
/ Cells (Biology)
/ Cells - metabolism
/ Cellular structure
/ Computer Simulation
/ Confocal microscopy
/ Cytoplasm
/ Cytoplasm - metabolism
/ Cytosol
/ Diffusion
/ Diffusion coefficient
/ Fluid dynamics
/ Fluorescence
/ Fluorescence Recovery After Photobleaching
/ Fluorescence spectroscopy
/ HeLa Cells
/ Humans
/ Image Processing, Computer-Assisted
/ Laboratories
/ Luminescent Proteins - metabolism
/ Mammals - metabolism
/ Mathematical models
/ Medical research
/ Microscopy
/ Microscopy, Confocal
/ Microscopy, Fluorescence
/ Models, Biological
/ Nuclei
/ Nuclei (cytology)
/ Numerical methods
/ Physics
/ Porosity
/ Protein binding
/ Proteins
/ Proteins - metabolism
/ Reproducibility of Results
/ Spectroscopy
/ Spectrum analysis
/ Three dimensional models
/ Viscoelasticity
2011
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Protein Diffusion in Mammalian Cell Cytoplasm
by
Dross, Nicolas
, Willman, Sami F.
, Kühn, Thomas
, Langowski, Jörg
, Vihinen-Ranta, Maija
, Ihalainen, Teemu O.
, Hyväluoma, Jari
, Timonen, Jussi
in
Animals
/ Bacterial Proteins - metabolism
/ Binding sites
/ Biology
/ Biophysics
/ Cats
/ Cell lines
/ Cells (Biology)
/ Cells - metabolism
/ Cellular structure
/ Computer Simulation
/ Confocal microscopy
/ Cytoplasm
/ Cytoplasm - metabolism
/ Cytosol
/ Diffusion
/ Diffusion coefficient
/ Fluid dynamics
/ Fluorescence
/ Fluorescence Recovery After Photobleaching
/ Fluorescence spectroscopy
/ HeLa Cells
/ Humans
/ Image Processing, Computer-Assisted
/ Laboratories
/ Luminescent Proteins - metabolism
/ Mammals - metabolism
/ Mathematical models
/ Medical research
/ Microscopy
/ Microscopy, Confocal
/ Microscopy, Fluorescence
/ Models, Biological
/ Nuclei
/ Nuclei (cytology)
/ Numerical methods
/ Physics
/ Porosity
/ Protein binding
/ Proteins
/ Proteins - metabolism
/ Reproducibility of Results
/ Spectroscopy
/ Spectrum analysis
/ Three dimensional models
/ Viscoelasticity
2011
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Protein Diffusion in Mammalian Cell Cytoplasm
by
Dross, Nicolas
, Willman, Sami F.
, Kühn, Thomas
, Langowski, Jörg
, Vihinen-Ranta, Maija
, Ihalainen, Teemu O.
, Hyväluoma, Jari
, Timonen, Jussi
in
Animals
/ Bacterial Proteins - metabolism
/ Binding sites
/ Biology
/ Biophysics
/ Cats
/ Cell lines
/ Cells (Biology)
/ Cells - metabolism
/ Cellular structure
/ Computer Simulation
/ Confocal microscopy
/ Cytoplasm
/ Cytoplasm - metabolism
/ Cytosol
/ Diffusion
/ Diffusion coefficient
/ Fluid dynamics
/ Fluorescence
/ Fluorescence Recovery After Photobleaching
/ Fluorescence spectroscopy
/ HeLa Cells
/ Humans
/ Image Processing, Computer-Assisted
/ Laboratories
/ Luminescent Proteins - metabolism
/ Mammals - metabolism
/ Mathematical models
/ Medical research
/ Microscopy
/ Microscopy, Confocal
/ Microscopy, Fluorescence
/ Models, Biological
/ Nuclei
/ Nuclei (cytology)
/ Numerical methods
/ Physics
/ Porosity
/ Protein binding
/ Proteins
/ Proteins - metabolism
/ Reproducibility of Results
/ Spectroscopy
/ Spectrum analysis
/ Three dimensional models
/ Viscoelasticity
2011
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Journal Article
Protein Diffusion in Mammalian Cell Cytoplasm
2011
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Overview
We introduce a new method for mesoscopic modeling of protein diffusion in an entire cell. This method is based on the construction of a three-dimensional digital model cell from confocal microscopy data. The model cell is segmented into the cytoplasm, nucleus, plasma membrane, and nuclear envelope, in which environment protein motion is modeled by fully numerical mesoscopic methods. Finer cellular structures that cannot be resolved with the imaging technique, which significantly affect protein motion, are accounted for in this method by assigning an effective, position-dependent porosity to the cell. This porosity can also be determined by confocal microscopy using the equilibrium distribution of a non-binding fluorescent protein. Distinction can now be made within this method between diffusion in the liquid phase of the cell (cytosol/nucleosol) and the cytoplasm/nucleoplasm. Here we applied the method to analyze fluorescence recovery after photobleach (FRAP) experiments in which the diffusion coefficient of a freely-diffusing model protein was determined for two different cell lines, and to explain the clear difference typically observed between conventional FRAP results and those of fluorescence correlation spectroscopy (FCS). A large difference was found in the FRAP experiments between diffusion in the cytoplasm/nucleoplasm and in the cytosol/nucleosol, for all of which the diffusion coefficients were determined. The cytosol results were found to be in very good agreement with those by FCS.
Publisher
Public Library of Science,Public Library of Science (PLoS)
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