2004
DOI: 10.1002/cphc.200400213
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Probing Ligand–Protein Recognition with Sum‐Frequency Generation Spectroscopy: The Avidin–Biocytin Case

Abstract: Infrared/visible sum-frequency generation (SFG) spectroscopy is used to study the recognition of a protein (avidin) by a derived vitamin (biocytin) adsorbed on a calcium fluoride substrate. The specificity of the process is tested by replacing avidin with bovine serum albumin or presaturated avidin. The SFG spectroscopy shows drastic modifications in the CH and NH spectral ranges only upon exposure of the biocytin film to avidin. The comparison of the SFG data with Fourier transform infrared reflection absorpt… Show more

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Cited by 42 publications
(31 citation statements)
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“…AuNps were deposited either on silicon in external reflection configuration [4] or on glass substrates in total internal reflection configuration [5] to compare the sensitivity and molecular ordering of functionalized AuNp films as a function of the surface coverage on glass [6], to unravel the orientation of grafted molecules on AuNps and AgNps [7] and to extract and deduce the nature of the vibration modes thanks to the SPR amplification on functionalized AuNp films in the fingerprint spectral range of aromatic molecules with density functional theory (DFT) calculations [8]. In a general way, SFG has also proven its efficiency in biomolecular recognition on glass substrate [9], in DNAbased biosensors on Pt(111) single crystal [10] and in enlightening DNA hybridization on glass [11] and (100)-facetted gold films [12]. In summary, SFG/DFG spectroscopy is a promising tool in describing the chemistry occurring in biological recognition [13,14] performed on nanostructured biosensors provided that we light on/off the SPR amplification in a controlled manner: AuNps nature, size, shape, and dispersion (surface coverage and lattice parameter) on the substrate, exciting visible wavelength.…”
Section: Introductionmentioning
confidence: 99%
“…AuNps were deposited either on silicon in external reflection configuration [4] or on glass substrates in total internal reflection configuration [5] to compare the sensitivity and molecular ordering of functionalized AuNp films as a function of the surface coverage on glass [6], to unravel the orientation of grafted molecules on AuNps and AgNps [7] and to extract and deduce the nature of the vibration modes thanks to the SPR amplification on functionalized AuNp films in the fingerprint spectral range of aromatic molecules with density functional theory (DFT) calculations [8]. In a general way, SFG has also proven its efficiency in biomolecular recognition on glass substrate [9], in DNAbased biosensors on Pt(111) single crystal [10] and in enlightening DNA hybridization on glass [11] and (100)-facetted gold films [12]. In summary, SFG/DFG spectroscopy is a promising tool in describing the chemistry occurring in biological recognition [13,14] performed on nanostructured biosensors provided that we light on/off the SPR amplification in a controlled manner: AuNps nature, size, shape, and dispersion (surface coverage and lattice parameter) on the substrate, exciting visible wavelength.…”
Section: Introductionmentioning
confidence: 99%
“…3043 Recently, SFG has also been employed to study biomolecules such as lipids, peptides and proteins which further progressed this research field. 4461 This article presents an overview of studies that have been done in our group that sheds light on elucidating molecular level information about interfacial peptides/proteins involved in different biological environments as well as processes.…”
Section: Introductionmentioning
confidence: 99%
“…The binding time was fixed at 22 h with stirring, followed by the washing and rinsing steps with HEPES and DI, respectively. Before starting the scanning process, the slides were stored to rest for 30 min in the printer [23].…”
Section: Biotin-strepavidin Reactionmentioning
confidence: 99%