首页> 外文期刊>Journal of Inorganic Biochemistry: An Interdisciplinary Journal >Solution interactions between the uranyl cation [UO22+] and histidine, N-acetyl-histidine, tyrosine, and N-acetyl-tyrosine
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Solution interactions between the uranyl cation [UO22+] and histidine, N-acetyl-histidine, tyrosine, and N-acetyl-tyrosine

机译:铀酰阳离子[UO22 +]与组氨酸,N-乙酰基组氨酸,酪氨酸和N-乙酰基酪氨酸之间的溶液相互作用

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Complexes of the uranyl cation [UO22+] with histidine (His), N-acetyl-histidine (NAH), tyrosine (Tyr), and N-acetyl-tyrosine (NAT) were studied by UV-visible and NMR spectroscopy, and by potentiometric titration. Protonation constants for each ligand are reported, as are cumulative formation constants for uranyl-amino acid complexes. Coupling constant data (J(CH)) for uranyl-histidine complexes indicate that inner-sphere solution interactions between histidine and uranyl cation are solely at the carboxylate site. At 25 C the major uranyl-histidine complex has a cumulative formation constant of log beta(110)=8.53, and a proposed formula of [UO(2)HisH(2)(OH)(2)](+); the stepwise formation constant, log K-UL, is estimated to be <= 5.6 (approximate to 8.53 -(-6.1) - (-6.1) - 15.15). Outer-sphere interactions, H-bonding or electrostatic interactions, are proposed as contributing a significant portion of the stability to the ternary uranyl-hydroxo-amino acid complexes. The temperature dependent protonation constants of histidine and formation constants between uranyl cation and histidine are reported from 10 to 35 degrees C; at 25 degrees C, Delta G=-43.3 kJ/mol. (c) 2008 Elsevier Inc. All rights reserved.
机译:通过UV-可见光谱和NMR光谱以及电位分析法研究了铀酰阳离子[UO22 +]与组氨酸(His),N-乙酰基组氨酸(NAH),酪氨酸(Tyr)和N-乙酰基酪氨酸(NAT)的配合物。滴定。报告了每个配体的质子化常数,以及铀酰-氨基酸复合物的累积形成常数。铀酰-组氨酸配合物的耦合常数数据(J(CH))表明,组氨酸和铀酰阳离子之间的内球溶液相互作用仅在羧酸酯位点处。在25°C时,主要的铀酰-组氨酸配合物的累积形成常数为log beta(110)= 8.53,[UO(2)HisH(2)(OH)(2)](+)的建议式为:逐步形成常数log K-UL估计为<= 5.6(约8.53-(-6.1)-(-6.1)-15.15)。提出外球相互作用,H键或静电相互作用为三元铀酰-羟基-氨基酸配合物贡献了很大一部分稳定性。据报道,从10到35摄氏度,组氨酸的温度依赖性质子化常数以及铀酰阳离子和组氨酸之间的形成常数。在25℃下,ΔG= -43.3kJ / mol。 (c)2008 Elsevier Inc.保留所有权利。

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