| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
Biophys J, December 1999, p. 3350-3355, Vol. 77, No. 6
Laboratoire d'Electrochimie, Ecole Polytechnique Fédérale de Lausanne, CH-1015 Lausanne, Switzerland
We present a study of the adsorption of the glucose
oxidase enzyme (GOx) at the air/water interface, using the nonlinear
optical technique of surface second harmonic generation (SSHG).
Resonant SSHG experiments were achieved by probing the
-
*
transition of the flavin adenine dinucleotide (FAD) chromophores
embedded in the GOx protein. Because of the subsequent resonance
enhancement of the signal, the second harmonic (SH) wave arising from
the GOx entities adsorbed at the interface was detectable for protein bulk aqueous concentrations as low as 70 nM. The protein adsorption was
followed, and, at high GOx coverage, a change in the orientation of the
FAD chromophore was observed, indicating either a rearrangement or a
reorientation of the protein at the interface. Inasmuch as GOx is
negatively charged at the biological pH of 7, its interactions with
charged surfactants were also investigated. As expected, spreading
positively charged surfactants onto a partial protein monolayer was
found to increase the GOx surface concentration, whereas in the case of
negatively charged surfactants, the GOx surface concentration decreased
until the SH signal went back to the pure buffer solution response
level. With the increasing GOx surface concentration, the rearrangement
or reorientation of the protein was also observed.
Biophys J, December 1999, p. 3350-3355, Vol. 77, No. 6
© 1999 by the Biophysical Society 0006-3495/99/12/3350/06 $2.00
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |