posted on 2015-12-01, 00:00authored byMatthew
C. D. Carter, Daniel S. Miller, James Jennings, Xiaoguang Wang, Mahesh K. Mahanthappa, Nicholas L. Abbott, David M. Lynn
We report synthetic
six-tailed mimics of the bacterial glycolipid
Lipid A that trigger changes in the internal ordering of water-dispersed
liquid crystal (LC) microdroplets at ultralow (picogram-per-milliliter)
concentrations. These molecules represent the first class of synthetic
amphiphiles to mimic the ability of Lipid A and bacterial endotoxins
to trigger optical responses in LC droplets at these ultralow concentrations.
This behavior stands in contrast to all previously reported synthetic
surfactants and lipids, which require near-complete monolayer coverage
at the LC droplet surface to trigger ordering transitions. Surface-pressure
measurements and SAXS experiments reveal these six-tailed synthetic
amphiphiles to mimic key aspects of the self-assembly of Lipid A at
aqueous interfaces and in solution. These and other results suggest
that these amphiphiles trigger orientational transitions at ultralow
concentrations through a unique mechanism that is similar to that
of Lipid A and involves formation of inverted self-associated nanostructures
at topological defects in the LC droplets.