V. Ball et Jj. Ramsden, ABSENCE OF SURFACE EXCLUSION IN THE FIRST STAGE OF LYSOZYME ADSORPTION IS DRIVEN THROUGH ELECTROSTATIC SELF-ASSEMBLY, JOURNAL OF PHYSICAL CHEMISTRY B, 101(28), 1997, pp. 5465-5469
Adsorption kinetics of hen egg white lysozyme at pH 7.4 onto a Si(Ti)O
-2 surface were measured at two ionic strengths and under different sh
ear rates by means of optical waveguide lightmode spectroscopy. At low
ionic strength, increases of the adsorbed amount linear with time sug
gest that the adsorption proceeds without surface exclusion. Within th
e concentration range investigated, the duration of this linear regime
was inversely proportional to the bulk concentration. The Linear regi
me always stopped at a threshold value of 0.18 +/- 0.02 mu g/cm(2) and
was followed by a second regime with surface exclusion. I At high ion
ic strength the linear regime was not observed, suggesting an electros
tatically driven self-assembly process at low ionic strength. This con
clusion is supported by the linear arrays of lysozyme at graphite surf
aces observed with STM (Haggerty, L.; Lenhoff, A. M. Biophys. J. 1993,
64, 886). Moreover, the adsorption rate at low ionic strength is fast
er than that predicted by diffusion across the diffusion boundary laye
r, suggesting that the transport is accelerated by electrostatic attra
ction. This was confirmed by an estimation of the electrostatic free e
nergy contribution.