An attempt has been made using Fourier transform infrared-attenuated t
otal reflection (FTIR-ATR) spectroscopy to see the molecular level int
eraction between indolicidin, a tridecapeptide known to possess antimi
crobial activity, and model phospholipid bilayers. Initially, model li
pid bilayers were assembled on ZnSe plates with compounds of dipalmito
ylphosphatidic acid (DPPA), dipalmitoylphosphatidylcholine (DPPC), and
dipalmitoylphosphatidylglycerol (DPPG) using the Langmuir-Blodgett (L
B) method. From the FTIR-ATR dichroic ratios measured with and without
rotation of the ATR plates, the LB lipid bilayers seemed to be descri
bed in terms of a uniaxial orientational model. Along with a cyclovolt
ammetry measurement, the ATR spectra dictated that indolicidin molecul
es were readily incorporated inside the acyl chains of the lipid bilay
ers. Furthermore, from the infrared absorption frequencies of amide I
bands, indolicidin molecules that consisted of ill-defined random-coil
structures in an aqueous medium appeared to adopt a 3(10)-helical con
formation inside the lipid bilayers. This view was in good agreement w
ith the electronic circular dichroism observed for PC (+10% cardiolipi
n) vesicles mixed with an indolicidin solution.