Tyndall National Institute, Lee Maltings, University College, Cork, Ireland.
Analyst. 2009 Aug;134(8):1608-13. doi: 10.1039/b905441n. Epub 2009 Jun 15.
The interaction of proteins with interfaces and surfaces provides a basis for studying their behaviour and methods to detect them. This paper is concerned with elucidation of the mechanism of electrochemical detection of haemoglobin (Hb) at the interface between aqueous and organic electrolyte solutions. The adsorption of Hb at the interface was investigated by alternating current (AC) voltammetry. It was found that addition of Hb to the aqueous phase induced a shift of the potential of zero charge at the liquid/liquid interface, due to interfacial adsorption of Hb. The influence of the nature and the concentration of the organic phase electrolyte on the electrochemical signal was investigated by cyclic voltammetry (CV). It was found that the electrochemical signal, in the presence of aqueous phase Hb, was due to the facilitated transfer of the anion of the organic phase electrolyte to the aqueous phase. The transfer current was dependent on both the nature and concentration of the organic phase electrolyte anion. These results confirm that adsorbed Hb molecules at the liquid/liquid interface interact with small ionised molecules and facilitate their transfer across the interface. The results will provide a basis for both biomolecular detection methods and for the study of protein-small ionised molecule interactions.
蛋白质与界面和表面的相互作用为研究它们的行为和检测它们的方法提供了基础。本文致力于阐明在水相和有机电解质溶液界面电化学检测血红蛋白(Hb)的机制。通过交流(AC)伏安法研究了 Hb 在界面上的吸附。结果发现,由于 Hb 在界面上的吸附,向水相添加 Hb 会导致液/液界面零电荷电位发生偏移。通过循环伏安法(CV)研究了有机相电解质的性质和浓度对电化学信号的影响。结果发现,在存在水相 Hb 的情况下,电化学信号是由于有机相电解质阴离子向水相的促进转移。转移电流既取决于有机相电解质阴离子的性质又取决于其浓度。这些结果证实,在液/液界面吸附的 Hb 分子与小离解分子相互作用,并促进它们穿过界面转移。这些结果将为生物分子检测方法以及蛋白质-小离解分子相互作用的研究提供基础。