Adsorption kinetics of human vimentin on negatively charged
substrates
(mica, silica, and polymer particles) was analyzed using atomic force
microscopy (AFM), quartz microbalance (QCM), and the laser doppler
velocimetry (LDV) method. AFM studies realized under diffusion conditions
proved that the adsorbed protein layer mainly consisted of aggregates
in the form of compact tetramers and hexamers of a size equal to 11–12
nm. These results were consistent with vimentin adsorption kinetics
under flow conditions investigated by QCM. It was established that
vimentin aggregates efficiently adsorbed on the negatively charged
silica sensor at pH 3.5 and 7.4, forming compact layers with the coverage
reaching 3.5 mg m
–2
. Additionally, the formation
of the vimentin corona at polymer particles was examined using the
LDV method and interpreted in terms of the electrokinetic model. This
allowed us to determine the zeta potential of the corona as a function
of pH and the electrokinetic charge of aggregates, which was equal
to −0.7 e nm
–2
at pH 7.4 in a 10 mM NaCl
solution. The anomalous adsorption of aggregates exhibiting an average
negative charge on the negatively charged substrates was interpreted
as a result of a heterogeneous charge distribution. These investigations
confirmed that it is feasible to deposit stable vimentin layers both
at planar substrates and at carrier particles with well-controlled
coverage and zeta potential. They can be used for investigations of
vimentin interactions with various ligands including receptors of
the innate immune system, immunoglobulins, bacterial virulence factors,
and spike proteins of viruses.