School of Chemistry , Joseph Black Building, University of Glasgow , Glasgow G12 8QQ , United Kingdom.
School of Engineering , Rankine Building, University of Glasgow , Glasgow G12 8LT , United Kingdom.
J Am Chem Soc. 2018 Jul 11;140(27):8509-8517. doi: 10.1021/jacs.8b03634. Epub 2018 Jun 29.
The structural order of biopolymers, such as proteins, at interfaces defines the physical and chemical interactions of biological systems with their surroundings and is hence a critical parameter in a range of biological problems. Known spectroscopic methods for routine rapid monitoring of structural order in biolayers are generally only applied to model single-component systems that possess a spectral fingerprint which is highly sensitive to orientation. This spectroscopic behavior is not a generic property and may require the addition of a label. Importantly, such techniques cannot readily be applied to real multicomponent biolayers, have ill-defined or unknown compositions, and have complex spectroscopic signatures with many overlapping bands. Here, we demonstrate the sensitivity of plasmonic fields with enhanced chirality, a property referred to as superchirality, to global orientational order within both simple model and "real" complex protein layers. The sensitivity to structural order is derived from the capability of superchiral fields to detect the anisotropic nature of electric dipole-magnetic dipole response of the layer; this is validated by numerical simulations. As a model study, the evolution of orientational order with increasing surface density in layers of the antibody immunoglobulin G was monitored. As an exemplar of greater complexity, superchiral fields are demonstrated, without knowledge of exact composition, to be able to monitor how qualitative changes in composition alter the structural order of protein layers formed from blood serum, thereby establishing the efficacy of the phenomenon as a tool for studying complex biological interfaces.
生物聚合物(如蛋白质)在界面处的结构有序性决定了生物系统与其周围环境的物理和化学相互作用,因此是一系列生物学问题的关键参数。已知的用于常规快速监测生物层结构有序性的光谱方法通常仅适用于具有高度敏感取向的光谱指纹的单组分体系。这种光谱行为不是通用特性,可能需要添加标签。重要的是,此类技术不能轻易应用于真正的多组分生物层,因为这些生物层的组成不确定或未知,并且具有复杂的光谱特征,其中包含许多重叠的谱带。在这里,我们展示了增强手性的等离子体场(称为超手性)对简单模型和“真实”复杂蛋白质层中整体各向有序性的敏感性。对手性有序性的敏感性源于超手性场检测层的电偶极-磁偶极响应各向异性的能力;这通过数值模拟得到验证。作为模型研究,监测了抗体免疫球蛋白 G 层中随着表面密度增加而引起的取向有序性的演变。作为更复杂的范例,即使不知道确切的组成,超手性场也能够监测组成的定性变化如何改变由血清形成的蛋白质层的结构有序性,从而确立该现象作为研究复杂生物界面的工具的功效。