The effects of globotriaosylceramide tail saturation level on bilayer phases

Weria Pezeshkian, Vitaly V. Chaban, Ludger Johannes, Julian Shillcock, John H. Ipsena, Himanshu Khandelia*

*Corresponding author for this work

Research output: Contribution to journalJournal articleResearchpeer-review

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Abstract

Globotriaosylceramide (Gb(3)) is a glycosphingolipid present in the plasma membrane that is the natural receptor of the bacterial Shiga toxin. The unsaturation level of Gb(3) acyl chains has a drastic impact on lipid bilayer properties and phase behaviour, and on many Gb(3)-related cellular processes. For example: the Shiga toxin B subunit forms tubular invaginations in the presence of Gb(3) with an unsaturated acyl chain (U-Gb(3)), while in the presence of Gb(3) with a saturated acyl chain (S-Gb(3)) such invagination does not occur. We have used all-atom molecular dynamics simulations to investigate the effects of the Gb(3) concentration and its acyl chain saturation on the phase behaviour of a mixed bilayer of dioleoylphosphatidylcholine and Gb(3). The simulation results show that: (1) the Gb(3) acyl chains (longer tails) from one leaflet interdigitate into the opposing leaflet and lead to significant bilayer rigidification and immobilisation of the lipid tails. S-Gb(3) can form a highly ordered, relatively immobile phase which is resistant to bending while these changes for U-Gb(3) are not significant. (2) At low concentrations of Gb(3), U-Gb(3) and S-Gb(3) have a similar impact on the bilayer reminiscent of the effect of sphingomyelin lipids and (3) At higher Gb(3) concentrations, U-Gb(3) mixes better with dioleoylphosphatidylcholine than S-Gb(3). Our simulations also provide the first molecular level structural model of Gb(3) in membranes.

Original languageEnglish
JournalSoft Matter
Volume11
Issue number7
Pages (from-to)1352-1361
Number of pages10
ISSN1744-683X
DOIs
Publication statusPublished - 2015
Externally publishedYes

Keywords

  • FORCE-FIELD
  • MOLECULAR-DYNAMICS
  • B-SUBUNIT
  • MEMBRANE
  • GROMACS
  • RECEPTOR
  • CHAIN
  • SPHINGOMYELIN
  • VALIDATION
  • ANTIGEN

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