Bernhardt Paul V, Chen Kuan-I, Sharpe Philip C
Centre for Metals in Biology, Department of Chemistry, University of Queensland, Brisbane, 4072, QLD, Australia.
J Biol Inorg Chem. 2006 Oct;11(7):930-6. doi: 10.1007/s00775-006-0148-z. Epub 2006 Jul 26.
A selection of nine macrocyclic Fe(III/II) and Co(III/II) transition metal complexes has been chosen to serve as a universal set of mediator-titrants in redox potentiometry of protein samples. The potential range spanned by these mediators is approximately from +300 to -700 mV vs the normal hydrogen electrode, which covers the range of most protein redox potentials accessible in aqueous solution. The complexes employed exhibit stability in both their oxidized and their reduced forms as well as pH-independent redox potentials within the range 6 < pH < 9. The mediators were also chosen on the basis of their very weak visible absorption maxima in both oxidation states, which will enable (for the first time) optical redox potentiometric titrations of proteins with relatively low extinction coefficients. This has previously been impractical with organic mediators, such as indoles, viologens and quinones, whose optical spectra interfere strongly with those of the protein.
已选择九种大环铁(III/II)和钴(III/II)过渡金属配合物作为蛋白质样品氧化还原电位滴定法中的通用介体滴定剂。相对于标准氢电极,这些介体的电位范围约为+300至-700 mV,这涵盖了水溶液中大多数可及的蛋白质氧化还原电位范围。所使用的配合物在氧化态和还原态均表现出稳定性,并且在6 < pH < 9范围内具有与pH无关的氧化还原电位。选择这些介体还基于它们在两种氧化态下都非常弱的可见吸收最大值,这将首次实现对具有相对低消光系数的蛋白质进行光学氧化还原电位滴定。以前使用有机介体(如吲哚、紫精和醌)进行这种滴定是不切实际的,因为它们的光谱会强烈干扰蛋白质的光谱。