A particle-based computational model to analyse remodelling of the red blood cell cytoskeleton during malaria infections

Red blood cells can withstand the harsh mechanical conditions in the vasculature only because the bending rigidity of their plasma membrane is complemented by the shear elasticity of the underlying spectrin-actin network. During an infection by the malaria parasite Plasmodium falciparum, the parasit...

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Main Authors: Jäger, Julia (Author) , Patra, Pintu (Author) , Sanchez, Cecilia P. (Author) , Lanzer, Michael (Author) , Schwarz, Ulrich S. (Author)
Format: Article (Journal)
Language:English
Published: April 8, 2022
In: PLoS Computational Biology
Year: 2022, Volume: 18, Issue: 4, Pages: 1-27
ISSN:1553-7358
DOI:10.1371/journal.pcbi.1009509
Online Access:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1371/journal.pcbi.1009509
Verlag, lizenzpflichtig, Volltext: https://journals.plos.org/ploscompbiol/article?id=10.1371/journal.pcbi.1009509
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Author Notes:Julia Jäger, Pintu Patra, Cecilia P. Sanchez, Michael Lanzer, Ulrich S. Schwarz
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Summary:Red blood cells can withstand the harsh mechanical conditions in the vasculature only because the bending rigidity of their plasma membrane is complemented by the shear elasticity of the underlying spectrin-actin network. During an infection by the malaria parasite Plasmodium falciparum, the parasite mines host actin from the junctional complexes and establishes a system of adhesive knobs, whose main structural component is the knob-associated histidine rich protein (KAHRP) secreted by the parasite. Here we aim at a mechanistic understanding of this dramatic transformation process. We have developed a particle-based computational model for the cytoskeleton of red blood cells and simulated it with Brownian dynamics to predict the mechanical changes resulting from actin mining and KAHRP-clustering. Our simulations include the three-dimensional conformations of the semi-flexible spectrin chains, the capping of the actin protofilaments and several established binding sites for KAHRP. For the healthy red blood cell, we find that incorporation of actin protofilaments leads to two regimes in the shear response. Actin mining decreases the shear modulus, but knob formation increases it. We show that dynamical changes in KAHRP binding affinities can explain the experimentally observed relocalization of KAHRP from ankyrin to actin complexes and demonstrate good qualitative agreement with experiments by measuring pair cross-correlations both in the computer simulations and in super-resolution imaging experiments.
Item Description:Gesehen am 10.06.2022
Physical Description:Online Resource
ISSN:1553-7358
DOI:10.1371/journal.pcbi.1009509