Nanovesicles (∼100 nm) are ubiquitous in cell biology and
an important vector for drug delivery. Mechanical properties of vesicles
are known to influence cellular uptake, but the mechanism by which
deformation dynamics affect internalization is poorly understood.
This is partly due to the fact that experimental studies of the mechanics
of such vesicles remain challenging, particularly at the nanometer
scale where appropriate theoretical models have also been lacking.
Here, we probe the mechanical properties of nanoscale liposomes using
atomic force microscopy (AFM) indentation. The mechanical response
of the nanovesicles shows initial linear behavior and subsequent flattening
corresponding to inward tether formation. We derive a quantitative
model, including the competing effects of internal pressure and membrane
bending, that corresponds well to these experimental observations.
Our results are consistent with a bending modulus of the lipid bilayer
of ∼14kbT. Surprisingly,
we find that vesicle stiffness is pressure dominated for adherent
vesicles under physiological conditions. Our experimental method and
quantitative theory represents a robust approach to study the mechanics
of nanoscale vesicles, which are abundant in biology, as well as being
of interest for the rational design of liposomal vectors for drug
delivery.