Polymerization
enhances the stability of a planar supported lipid
bilayer (PSLB) but it also changes its chemical and mechanical properties,
attenuates lipid diffusion, and may affect the activity of integral
membrane proteins. Mixed bilayers composed of fluid lipids and poly(lipids)
may provide an appropriate combination of polymeric stability coupled
with the fluidity and elasticity needed to maintain the bioactivity
of reconstituted receptors. Previously (Langmuir, 2019, 35, 12483–12491) we showed that
binary mixtures of the polymerizable lipid bis-SorbPC and the fluid
lipid DPhPC form phase-segregated PSLBs composed of nanoscale fluid
and poly(lipid) domains. Here we used atomic force microscopy (AFM)
to compare the nanoscale mechanical properties of these binary PSLBs
with single-component PSLBs. The elastic (Young’s) modulus,
area compressibility modulus, and bending modulus of bis-SorbPC PSLBs
increased upon polymerization. Before polymerization, breakthrough
events at forces below 5 nN were observed, but after polymerization,
the AFM tip could not penetrate the PSLB up to an applied force of
20 nN. These results are attributed to the polymeric network in poly(bis-SorbPC),
which increases the bilayer stiffness and resists compression and
bending. In binary DPhPC/poly(bis-SorbPC) PSLBs, the DPhPC domains
are less stiff, more compressible, and are less resistant to rupture
and bending compared to pure DPhPC bilayers. These differences are
attributed to bis-SorbPC monomers and oligomers present in DPhPC domains
that disrupt the packing of DPhPC molecules. In contrast, the poly(bis-SorbPC)
domains are stiffer and less compressible relative to pure PSLBs;
this difference is attributed to DPhPC filling the nm-scale pores
in the polymerized domains that are created during bis-SorbPC polymerization.
Thus, incomplete phase segregation increases the stability of poly(bis-SorbPC)
but has the opposite, detrimental effect for DPhPC. Overall, these
results provide guidance for the design of partially polymerized bilayers
for technological uses.