Erik B van Munster

Summary

Affiliation: University of Amsterdam
Country: The Netherlands

Publications

  1. ncbi Interferometry in flow to sort unstained X- and Y-chromosome-bearing bull spermatozoa
    Erik B van Munster
    Holland Genetics, Arnhem, The Netherlands
    Cytometry 47:192-9. 2002
  2. pmc Quantitative lifetime unmixing of multiexponentially decaying fluorophores using single-frequency fluorescence lifetime imaging microscopy
    Gert Jan Kremers
    Section Molecular Cytology and Centre for Advanced Microscopy, Swammerdam Institute for Life Sciences, University of Amsterdam, Kruislaan 316, NL 1098 SM, Amsterdam, The Netherlands
    Biophys J 95:378-89. 2008
  3. ncbi Fluorescence lifetime imaging microscopy (FLIM)
    Erik B van Munster
    Swammerdam Institute for Life Sciences and Centre for Advanced Microscopy, Section Molecular Cytology, Kruislaan 316, 1098 SM Amsterdam, The Netherlands
    Adv Biochem Eng Biotechnol 95:143-75. 2005
  4. ncbi phiFLIM: a new method to avoid aliasing in frequency-domain fluorescence lifetime imaging microscopy
    E B Van Munster
    Section Molecular Cytology, Swammerdam Institute for Life Sciences, University of Amsterdam, Kruislaan 316, 1098 SM, Amsterdam, The Netherlands
    J Microsc 213:29-38. 2004
  5. ncbi Suppression of photobleaching-induced artifacts in frequency-domain FLIM by permutation of the recording order
    Erik B van Munster
    Molecular Cytology Section, Swammerdam Institute for Life Sciences, University of Amsterdam, Amsterdam, The Netherlands
    Cytometry A 58:185-94. 2004
  6. ncbi Fluorescence resonance energy transfer (FRET) measurement by gradual acceptor photobleaching
    E B Van Munster
    Centre for Advanced Microscopy, Section Molecular Cytology, Swammerdam Institute for Life Sciences, University of Amsterdam, The Netherlands
    J Microsc 218:253-62. 2005
  7. ncbi Cyan and yellow super fluorescent proteins with improved brightness, protein folding, and FRET Förster radius
    Gert Jan Kremers
    Section Molecular Cytology and Centre for Advanced Microscopy, Swammerdam Institute for Life Sciences, University of Amsterdam, Kruislaan 316, 1098 SM, Amsterdam, The Netherlands
    Biochemistry 45:6570-80. 2006
  8. ncbi Imaging in situ protein-DNA interactions in the cell nucleus using FRET-FLIM
    Frédéric G E Cremazy
    Swammerdam Institute for Life Sciences, BioCentrum Amsterdam, University of Amsterdam, Kruislaan 318, 1098 SM Amsterdam, The Netherlands
    Exp Cell Res 309:390-6. 2005

Collaborators

Detail Information

Publications8

  1. ncbi Interferometry in flow to sort unstained X- and Y-chromosome-bearing bull spermatozoa
    Erik B van Munster
    Holland Genetics, Arnhem, The Netherlands
    Cytometry 47:192-9. 2002
    ..A novel technique is introduced combining interferometry with flow cytometry...
  2. pmc Quantitative lifetime unmixing of multiexponentially decaying fluorophores using single-frequency fluorescence lifetime imaging microscopy
    Gert Jan Kremers
    Section Molecular Cytology and Centre for Advanced Microscopy, Swammerdam Institute for Life Sciences, University of Amsterdam, Kruislaan 316, NL 1098 SM, Amsterdam, The Netherlands
    Biophys J 95:378-89. 2008
    ..The method is rigorously tested using samples of known composition and applied to live cell microscopy using cells expressing multiple (multiexponentially decaying) fluorescent proteins...
  3. ncbi Fluorescence lifetime imaging microscopy (FLIM)
    Erik B van Munster
    Swammerdam Institute for Life Sciences and Centre for Advanced Microscopy, Section Molecular Cytology, Kruislaan 316, 1098 SM Amsterdam, The Netherlands
    Adv Biochem Eng Biotechnol 95:143-75. 2005
    ..Other application areas, including usage of lifetime contrast for ion-imaging, quantitative imaging, tissue characterization and medical applications, are discussed...
  4. ncbi phiFLIM: a new method to avoid aliasing in frequency-domain fluorescence lifetime imaging microscopy
    E B Van Munster
    Section Molecular Cytology, Swammerdam Institute for Life Sciences, University of Amsterdam, Kruislaan 316, 1098 SM, Amsterdam, The Netherlands
    J Microsc 213:29-38. 2004
    ..Errors in lifetimes of YFP-transfected HeLa cells were as high as 100%. With phiFLIM, using the same specimen and settings, systematic errors due to aliasing did not occur...
  5. ncbi Suppression of photobleaching-induced artifacts in frequency-domain FLIM by permutation of the recording order
    Erik B van Munster
    Molecular Cytology Section, Swammerdam Institute for Life Sciences, University of Amsterdam, Amsterdam, The Netherlands
    Cytometry A 58:185-94. 2004
    ..A method is introduced that suppresses the effects of photobleaching without the need for extra recordings or processing...
  6. ncbi Fluorescence resonance energy transfer (FRET) measurement by gradual acceptor photobleaching
    E B Van Munster
    Centre for Advanced Microscopy, Section Molecular Cytology, Swammerdam Institute for Life Sciences, University of Amsterdam, The Netherlands
    J Microsc 218:253-62. 2005
    ....
  7. ncbi Cyan and yellow super fluorescent proteins with improved brightness, protein folding, and FRET Förster radius
    Gert Jan Kremers
    Section Molecular Cytology and Centre for Advanced Microscopy, Swammerdam Institute for Life Sciences, University of Amsterdam, Kruislaan 316, 1098 SM, Amsterdam, The Netherlands
    Biochemistry 45:6570-80. 2006
    ..Using the large lifetime difference between SCFP1 and SCFP3A enabled us to perform for the first time dual-lifetime imaging of spectrally identical fluorescent species in living cells...
  8. ncbi Imaging in situ protein-DNA interactions in the cell nucleus using FRET-FLIM
    Frédéric G E Cremazy
    Swammerdam Institute for Life Sciences, BioCentrum Amsterdam, University of Amsterdam, Kruislaan 318, 1098 SM Amsterdam, The Netherlands
    Exp Cell Res 309:390-6. 2005
    ..The method was successfully applied to the DNA-binding proteins histone H2B and the glucocorticoid receptor and to the heterochromatin-associated proteins HP1alpha and HP1beta...