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@ARTICLE{Abdollahzadeh:862657,
      author       = {Abdollahzadeh, Iman and Hendriks, Johnny and Sanwald, Julia
                      L. and Simons, Indra M. and Hoffmann, Silke and
                      Weiergräber, Oliver H. and Willbold, Dieter and Gensch,
                      Thomas},
      title        = {{A}utophagy-{R}elated {P}roteins {GABARAP} and {LC}3{B}
                      {L}abel {S}tructures of {S}imilar {S}ize but {D}ifferent
                      {S}hape in {S}uper-{R}esolution {I}maging},
      journal      = {Molecules},
      volume       = {24},
      number       = {9},
      issn         = {1420-3049},
      address      = {Basel},
      publisher    = {MDPI},
      reportid     = {FZJ-2019-02913},
      pages        = {1833 -},
      year         = {2019},
      abstract     = {Subcellular structures containing autophagy-related
                      proteins of the Atg8 protein family have been investigated
                      with conventional wide-field fluorescence and single
                      molecule localisation microscopy. Fusion proteins of GABARAP
                      and LC3B, respectively, with EYFP were overexpressed in
                      HEK293 cells. While size distributions of structures
                      labelled by the two proteins were found to be similar, shape
                      distributions appeared quite disparate, with EYFP-GABARAP
                      favouring circular structures and elliptical structures
                      being dominant for EYFP-LC3B. The latter also featured a
                      nearly doubled fraction of U-shape structures. The
                      experimental results point towards highly differential
                      localisation of the two proteins, which appear to label
                      structures representing distinct stages or even specific
                      channels of vesicular trafficking pathways. Our data also
                      demonstrate that the application of super-resolution
                      techniques expands the possibilities of fluorescence-based
                      methods in autophagy studies and in some cases can rectify
                      conclusions obtained from conventional fluorescence
                      microscopy with diffraction-limited resolution.},
      cin          = {ICS-6 / ICS-4},
      ddc          = {540},
      cid          = {I:(DE-Juel1)ICS-6-20110106 / I:(DE-Juel1)ICS-4-20110106},
      pnm          = {552 - Engineering Cell Function (POF3-552)},
      pid          = {G:(DE-HGF)POF3-552},
      typ          = {PUB:(DE-HGF)16},
      pubmed       = {pmid:31086037},
      UT           = {WOS:000469518100192},
      doi          = {10.3390/molecules24091833},
      url          = {https://juser.fz-juelich.de/record/862657},
}