Harris Wesley R, Wang Zhepeng, Hamada Yahia Z
Department of Chemistry and Biochemistry, University of Missouri-St. Louis, St. Louis, MO 63121, USA.
Inorg Chem. 2003 May 19;42(10):3262-73. doi: 10.1021/ic026027w.
A key issue regarding the speciation of Al(3+) in serum is how well the ligands citric acid and phosphate can compete with the iron transport protein serum transferrin for the aluminum. Previous studies have attempted to measure binding constants for each ligand separately, but experimental problems make it very difficult to obtain stability constants with the accuracy required to make a meaningful comparison between these ligands. In this study, effective binding constants for Al-citrate and Al-phosphate at pH 7.4 have been determined using difference UV spectroscopy to monitor the direct competition between these ligands and transferrin. The analysis of this competition equilibrium also includes the binding of citrate and phosphate as anions to apotransferrin. The effective binding constants are 10(11.59) for the 1:1 Al-citrate complexes and 10(14.90) for the 1:2 Al-citrate complexes. The effective binding constant for the 1:2 Al-phosphate complex is 10(12.02). No 1:1 Al-phosphate complex was detected. Speciation calculations based on these effective binding constants indicate that, at serum concentrations of citrate and phosphate, citrate will be the primary low-molecular-mass ligand for aluminum. Formal stability constants for the Al-citrate system have also been determined by potentiometric methods. This equilibrium system is quite complex, and information from both electrospray mass spectrometry and difference UV experiments has been used to select the best model for fitting the potentiometric data. The mass spectra contain peaks that have been assigned to complexes having aluminum:citrate stoichiometries of 1:1, 1:2, 2:2, 2:3, and 3:3. The difference UV results were used to determine the stability constant for Al(H(-1)cta)-, which was then used in the least-squares fitting of the potentiometric data to determine stability constants for Al(Hcta)+, Al(cta), Al(cta)2(3-), Al(H(-1)cta)(cta)(4-), Al2(H(-1)cta)2(2-), and Al3(H(-1)cta)3(OH)(4-).
血清中铝离子(Al(3+))形态的一个关键问题是,柠檬酸和磷酸这两种配体与铁转运蛋白血清转铁蛋白竞争铝离子的能力有多强。以往的研究试图分别测量每种配体的结合常数,但实验问题使得很难获得能在这些配体之间进行有意义比较所需精度的稳定常数。在本研究中,利用差分紫外光谱法监测这些配体与转铁蛋白之间的直接竞争,测定了pH 7.4条件下柠檬酸铝和磷酸铝的有效结合常数。对这种竞争平衡的分析还包括柠檬酸根和磷酸根阴离子与脱铁转铁蛋白的结合。1:1柠檬酸铝配合物的有效结合常数为10(11.59),1:2柠檬酸铝配合物的有效结合常数为10(14.90)。1:2磷酸铝配合物的有效结合常数为10(12.02)。未检测到1:1磷酸铝配合物。基于这些有效结合常数的形态计算表明,在血清中柠檬酸和磷酸的浓度下,柠檬酸将是铝的主要低分子量配体。柠檬酸铝体系的形式稳定常数也通过电位滴定法测定。这个平衡体系相当复杂,已利用电喷雾质谱和差分紫外实验的信息来选择拟合电位滴定数据的最佳模型。质谱中包含已被归属于铝:柠檬酸化学计量比为1:1、1:2、2:2、2:3和3:3的配合物峰。差分紫外结果用于确定Al(H(-1)cta)-的稳定常数,然后将其用于电位滴定数据的最小二乘拟合,以确定Al(Hcta)+、Al(cta)、Al(cta)2(3-)、Al(H(-1)cta)(cta)(4-)、Al2(H(-1)cta)2(2-)和Al3(H(-1)cta)3(OH)(4-)的稳定常数。