Wang Jie, Chen Xiaoyun, Clarke Matthew L, Chen Zhan
Department of Chemistry, University of Michigan, Ann Arbor, MI 48109, USA.
Proc Natl Acad Sci U S A. 2005 Apr 5;102(14):4978-83. doi: 10.1073/pnas.0501206102. Epub 2005 Mar 25.
In this work, we demonstrate the feasibility to collect off-electronic resonance chiral sum frequency generation (SFG) vibrational spectra from interfacial proteins and peptides at the solid/liquid interface in situ. It is difficult to directly detect a chiral SFG vibrational spectrum from interfacial fibrinogen molecules. By adopting an interference enhancement method, such a chiral SFG vibrational spectrum can be deduced from interference spectra between the normal achiral spectrum and the chiral spectrum. We found that the chiral SFG vibrational spectrum of interfacial fibrinogen was mainly contributed by the beta-sheet structure. For a beta-sheet peptide tachyplesin I, which may be quite ordered at the solid/liquid interface, chiral SFG vibrational spectra can be collected directly. We believe that these chiral signals are mainly contributed by electric dipole contributions, which can dominate the chiroptical responses of uniaxial systems. For the first time, to our knowledge, this work indicates that the off-electronic resonance SFG technique is sensitive enough to collect chiral SFG vibrational spectra of interfacial proteins and peptides, providing more structural information to elucidate interfacial protein and peptide structures.
在这项工作中,我们证明了原位收集固/液界面处界面蛋白和肽的离电子共振手性和频产生(SFG)振动光谱的可行性。直接检测界面纤维蛋白原分子的手性SFG振动光谱是困难的。通过采用干涉增强方法,可以从正常非手性光谱和手性光谱之间的干涉光谱中推导出这样的手性SFG振动光谱。我们发现界面纤维蛋白原的手性SFG振动光谱主要由β-折叠结构贡献。对于在固/液界面可能相当有序的β-折叠肽鲎素I,可以直接收集手性SFG振动光谱。我们认为这些手性信号主要由电偶极贡献,其可以主导单轴系统的手性光学响应。据我们所知,这项工作首次表明离电子共振SFG技术足够灵敏,能够收集界面蛋白和肽的手性SFG振动光谱,为阐明界面蛋白和肽的结构提供更多结构信息。