4.6 Article

Interactions of Bacterial Quorum Sensing Signals with Model Lipid Membranes: Influence of Acyl Tail Structure on Multiscale Response

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LANGMUIR
卷 37, 期 41, 页码 12049-12058

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AMER CHEMICAL SOC
DOI: 10.1021/acs.langmuir.1c01825

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资金

  1. National Science Foundation [DMR-1720415]
  2. NSF through the UW MRSEC [DMR-1720415]
  3. NIH [R35 GM131817]
  4. NSF [CHE-0342998]
  5. NSF Graduate Research Fellowship

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This study found that the length and oxidation state of AHL acyl tail groups influence their interactions with model lipid membranes, with the presence of a 3-oxo group impacting membrane remodeling. AHLs with 3-oxo groups generally promote microtubule formation, while AHLs without 3-oxo groups tend to form hemispherical caps on lipid bilayers. Additionally, 3-oxo AHLs showed greater association with lipid bilayers and facilitated greater transport or leakage of cargo molecules across membranes compared to non-3-oxo AHLs, indicating increased bilayer disruption and destabilization.
Many common bacteria use amphiphilic N-acyl-L-homoserine lactones (AHLs) as signaling molecules to coordinate group behaviors at high cell densities. Past studies demonstrate that AHLs can adsorb to and promote the remodeling of lipid membranes in ways that could underpin cell-cell or host-cell interactions. Here, we report that changes in AHL acyl tail group length and oxidation state (e.g., the presence or absence of a 3-oxo group) can lead to differences in the interactions of eight naturally occurring AHLs in solution and in contact with model lipid membranes. Our results reveal that the presence of a 3-oxo group impacts remodeling when AHLs are placed in contact with supported lipid bilayers (SLBs) of the phospholipid 1,2-dioleoyl-sn-glycero-3-phosphocholine (DOPC). Whereas AHLs that have 3-oxo groups generally promote the formation of microtubules, AHLs that lack 3-oxo groups generally form hemispherical caps on the surfaces of SLBs. These results are interpreted in terms of the time scales on which AHLs translocate across bilayers to relieve asymmetrical bilayer stress. Quartz crystal microbalance with dissipation measurements also reveal that 3-oxo AHLs associate with DOPC bilayers to a greater extent than their non-3-oxo analogues. In contrast, we observed no monotonic relationship between AHL tail length and bilayer reformation. Finally, we observed that 3-oxo AHLs facilitate greater transport or leakage of molecular cargo across the membranes of DOPC vesicles relative to AHLs without 3-oxo groups, also suggesting increased bilayer disruption and destabilization. These fundamental studies hint at interactions and associated multiscale phenomena that may inform current interpretations of the behaviors of AHLs in biological contexts. These results could also provide guidance useful for the design of new classes of synthetic materials (e.g., sensor elements or drug delivery vehicles) that interact with or respond selectively to communities of bacteria that use 3-oxo AHLs for cell-cell communication.

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