Total Internal Reflection Tip-Enhanced Raman Spectroscopy of Cytochromec
Author(s) -
David Talaga,
Andrew Bremner,
Thierry Buffeteau,
Renaud A. L. Vallée,
Sophie Lecomte,
Sébastien Bonhommeau
Publication year - 2020
Publication title -
the journal of physical chemistry letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.563
H-Index - 203
ISSN - 1948-7185
DOI - 10.1021/acs.jpclett.0c00579
Subject(s) - raman spectroscopy , biomolecule , total internal reflection , chemistry , monolayer , nanoscopic scale , hemeprotein , analytical chemistry (journal) , ferric , spectroscopy , resonance raman spectroscopy , molecule , photochemistry , materials science , heme , optics , nanotechnology , optoelectronics , inorganic chemistry , organic chemistry , physics , quantum mechanics , enzyme , biochemistry
Surface and tip-enhanced Raman spectroscopies in total internal reflection (TIR-SERS and TIR-TERS) are used to characterize the oxidation, spin, and ligation state of cytochrome c (Cc) molecules electrostatically bound on a hydrophilic thiol self-assembled monolayer. TIR-SERS spectra of this model hemoprotein show marker bands typical of the 6cLS ferric state of Cc. The performances of the TIR-TERS technique as a function of the incidence angle are described, showing in particular a significant electromagnetic enhancement of the Raman signal under p -polarized light excitation. TIR-TERS spectra of Cc confirm the 6cLS ferric state assignment deduced from TIR-SERS spectra, thus demonstrating the possibility of probing with nanoscale spatial resolution the 6cLS oxidized form of Cc that is potentially implicated in cell apoptotic processes. The minimal far-field contribution of the sample in TIR-TERS also offers promising perspectives for future nanoscale chemical characterizations of photosensitive biomolecules in complex biological media.
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