% IMPORTANT: The following is UTF-8 encoded.  This means that in the presence
% of non-ASCII characters, it will not work with BibTeX 0.99 or older.
% Instead, you should use an up-to-date BibTeX implementation like “bibtex8” or
% “biber”.

@ARTICLE{Dasanna:863773,
      author       = {Dasanna, Anil K. and Fedosov, Dmitry A. and Gompper,
                      Gerhard and Schwarz, Ulrich S.},
      title        = {{S}tate diagram for wall adhesion of red blood cells in
                      shear flow: from crawling to flipping},
      journal      = {Soft matter},
      volume       = {15},
      number       = {27},
      issn         = {1744-6848},
      address      = {London},
      publisher    = {Royal Soc. of Chemistry},
      reportid     = {FZJ-2019-03769},
      pages        = {5511 - 5520},
      year         = {2019},
      abstract     = {Red blood cells in shear flow show a variety of different
                      shapes due to the complex interplay between hydrodynamics
                      and membrane elasticity. Malaria-infected red blood cells
                      become generally adhesive and less deformable. Adhesion to a
                      substrate leads to a reduction in shape variability and to a
                      flipping motion of the non-spherical shapes during the
                      mid-stage of infection. Here, we present a complete state
                      diagram for wall adhesion of red blood cells in shear flow
                      obtained by simulations, using a particle-based mesoscale
                      hydrodynamics approach, multiparticle collision dynamics. We
                      find that cell flipping at a substrate is replaced by
                      crawling beyond a critical shear rate, which increases with
                      both membrane stiffness and viscosity contrast between the
                      cytosol and suspending medium. This change in cell dynamics
                      resembles the transition between tumbling and tank-treading
                      for red blood cells in free shear flow. In the context of
                      malaria infections, the flipping–crawling transition would
                      strongly increase the adhesive interactions with the
                      vascular endothelium, but might be suppressed by the
                      combined effect of increased elasticity and viscosity
                      contrast.},
      cin          = {ICS-2},
      ddc          = {530},
      cid          = {I:(DE-Juel1)ICS-2-20110106},
      pnm          = {552 - Engineering Cell Function (POF3-552)},
      pid          = {G:(DE-HGF)POF3-552},
      typ          = {PUB:(DE-HGF)16},
      pubmed       = {pmid:31241632},
      UT           = {WOS:000477949700005},
      doi          = {10.1039/C9SM00677J},
      url          = {https://juser.fz-juelich.de/record/863773},
}