TY - JOUR
T1 - Phase-Sensitive Detection in Modulation Excitation Spectroscopy Applied to Potential Induced Electron Transfer in Cytochrome c Oxidase
AU - Schwaighofer, Andreas
AU - Ferguson-Miller, Shelagh
AU - Naumann, Renate L. C.
AU - Knoll, Wolfgang
AU - Nowak, Christoph
PY - 2014
Y1 - 2014
N2 - Cytochrome c oxidase (CcO) from Rhodobacter sphaeroides was
investigated by modulated excitation surface-enhanced infraredabsorptionspectroscopy (SEIRAS). Sequential electron transfer
(ET) within CcO was initiated by electrochemical excitation. During
modulated excitation by periodic potential pulses with frequencies
between 20 and 500 Hz, time-resolved infrared spectra were
measured by the step-scan technique, with time resolution in the
millisecond range. Conformational changes of the protein structure
as a result of ET lead to rather complex SEIRA spectra with many
overlapping bands embedded in a broad background signal. Phasesensitive detection (PSD) was used to separate single components
within the broad band of overlapping structural bands in the amide I
region. PSD is able to extract the periodic response of single
components with the same frequency as the excitation from noise
or from static background and therefore enhances the signal-tonoise
ratio. Moreover, PSD enables validation of the fit model used
for the deconvolution of overlapping bands by analyzing phase
lags of single components acquired at different stimulation
frequencies. Phase lags between the evaluated vibrational components
and the modulated excitation increase with increasing
excitation frequencies, an inherent prerequisite of this evaluation
method.
Index Headings: Fourier transform infrared spectroscopy; FT-IR;
Surface-enhanced infrared-absorption spectroscopy; SEIRAS;
Phase-sensitive detection; PSD; Cytochrome c oxidase; CcO; Band
deconvolution; Modulation spectroscopy.
AB - Cytochrome c oxidase (CcO) from Rhodobacter sphaeroides was
investigated by modulated excitation surface-enhanced infraredabsorptionspectroscopy (SEIRAS). Sequential electron transfer
(ET) within CcO was initiated by electrochemical excitation. During
modulated excitation by periodic potential pulses with frequencies
between 20 and 500 Hz, time-resolved infrared spectra were
measured by the step-scan technique, with time resolution in the
millisecond range. Conformational changes of the protein structure
as a result of ET lead to rather complex SEIRA spectra with many
overlapping bands embedded in a broad background signal. Phasesensitive detection (PSD) was used to separate single components
within the broad band of overlapping structural bands in the amide I
region. PSD is able to extract the periodic response of single
components with the same frequency as the excitation from noise
or from static background and therefore enhances the signal-tonoise
ratio. Moreover, PSD enables validation of the fit model used
for the deconvolution of overlapping bands by analyzing phase
lags of single components acquired at different stimulation
frequencies. Phase lags between the evaluated vibrational components
and the modulated excitation increase with increasing
excitation frequencies, an inherent prerequisite of this evaluation
method.
Index Headings: Fourier transform infrared spectroscopy; FT-IR;
Surface-enhanced infrared-absorption spectroscopy; SEIRAS;
Phase-sensitive detection; PSD; Cytochrome c oxidase; CcO; Band
deconvolution; Modulation spectroscopy.
U2 - 10.1366/13-07188
DO - 10.1366/13-07188
M3 - Article
SN - 0003-7028
VL - 68
SP - 5
EP - 13
JO - Applied Spectroscopy
JF - Applied Spectroscopy
IS - 1
ER -