Varhac Rastislav, Antalík Marián
Department of Biochemistry, Faculty of Science, P. J. Safárik University, Moyzesova 11, 04001, Kosice, Slovakia.
J Biol Inorg Chem. 2008 Jun;13(5):713-21. doi: 10.1007/s00775-008-0357-8. Epub 2008 Mar 4.
A relation between pH-induced conformational transitions of horse heart ferricytochrome c and the kinetics of external ligand coordination to heme iron was investigated by optical spectroscopy, circular dichroism and viscometry. The dependencies of both the association, k (a), and dissociation rate constants of cyanide binding on pH were determined from kinetic measurements. The association rate constant exhibits a bell-shaped form of dependence on pH in the region where this protein unfolds. The maximum of the dependence of k (a) on pH is found to be coincident with the pK values of conformational transitions of ferricytochrome c in solutions with both low and high ionic strengths. This observation is explained in terms of ferricytochrome c unfolding, which is characterized by two processes: the gradual opening of the heme crevice accompanied by the detachment of the axial Met80 and its replacement with a water molecule. The former process enhances the rate, whereas the latter results in the inhibition of the rate of cyanide binding.
通过光谱学、圆二色性和粘度测定法研究了马心铁细胞色素c的pH诱导构象转变与外部配体与血红素铁配位动力学之间的关系。从动力学测量中确定了氰化物结合的缔合速率常数k(a)和解离速率常数对pH的依赖性。在该蛋白质展开的区域中,缔合速率常数呈现出对pH的钟形依赖性。发现k(a)对pH的依赖性最大值与低离子强度和高离子强度溶液中铁细胞色素c构象转变的pK值一致。这一观察结果是根据铁细胞色素c的展开来解释的,其特征在于两个过程:血红素裂隙的逐渐打开伴随着轴向甲硫氨酸80的脱离及其被水分子取代。前一个过程提高了速率,而后者导致氰化物结合速率的抑制。