Bieri Marco, Bürgi Thomas
Institut de Chimie, Faculté des Sciences, Université de Neuchâtel, Rue Emile-Argand 11, 2007 Neuchâtel, Switzerland.
Langmuir. 2005 Feb 15;21(4):1354-63. doi: 10.1021/la047735s.
Adsorption of the tripeptide L-glutathione (gamma-glu-cys-gly) on gold surfaces was investigated by polarization modulation infrared reflection absorption spectroscopy (PM-IRRAS) and attenuated total reflection (ATR) infrared spectroscopy. PM-IRRAS was used to study ex situ the adsorbate layer prepared from aqueous solutions at different pH, whereas ATR-IR was applied to study in situ adsorption from ethanol in the presence and absence of acid and base. ATR-IR was furthermore combined with modulation spectroscopy in order to investigate the reversible changes within the adsorbate layer induced by acid and base stimuli, respectively. The molecule is firmly anchored on the gold surface via the thiol group of the cys part. However, the ATR-IR spectra in ethanol indicate a further interaction with the gold surface via the carboxylic acid group of the gly part of the molecule, which deprotonates upon adsorption. Hydrochloric acid readily protonates the two acid groups of the adsorbed molecule. During subsequent ethanol flow the acid groups deprotonate again, a process which proceeds in two distinct steps: a fast step associated with the deprotonation of the acid in the glu part of the molecule and a considerably slower step associated with deprotonation of the acid in the gly moiety. The latter process is assisted by the interaction of the corresponding acid group with the surface. The spectra furthermore indicate a rearrangement of the hydrogen bonding network within the adsorbate layer upon deprotonation. Depending on the protonation state during adsorption of l-glutathione, the response toward identical protonation-deprotonation stimuli is significantly different. This is explained by the ionic state-dependent shape of the molecule, as supported by density functional theory calculations. The different shapes of the individual molecules during layer formation thus influence the structure of the adsorbate layer.
通过偏振调制红外反射吸收光谱(PM - IRRAS)和衰减全反射(ATR)红外光谱研究了三肽L - 谷胱甘肽(γ - glu - cys - gly)在金表面的吸附情况。PM - IRRAS用于非原位研究在不同pH值的水溶液中制备的吸附层,而ATR - IR则用于研究在有酸和碱存在及不存在的情况下乙醇中的原位吸附。此外,ATR - IR与调制光谱相结合,以分别研究酸和碱刺激引起的吸附层内的可逆变化。该分子通过cys部分的硫醇基团牢固地锚定在金表面。然而,乙醇中的ATR - IR光谱表明该分子的gly部分的羧酸基团与金表面进一步相互作用,该基团在吸附时会去质子化。盐酸很容易使吸附分子的两个酸基团质子化。在随后的乙醇流动过程中,酸基团再次去质子化,这个过程分两个不同的步骤进行:一个快速步骤与分子glu部分的酸去质子化相关,一个相当慢的步骤与gly部分的酸去质子化相关。后一个过程由相应酸基团与表面的相互作用辅助。光谱还表明去质子化后吸附层内氢键网络的重排。取决于L - 谷胱甘肽吸附过程中的质子化状态,对相同质子化 - 去质子化刺激的响应显著不同。密度泛函理论计算支持这是由分子的离子态依赖形状所解释的。因此,层形成过程中单个分子的不同形状影响了吸附层的结构。