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镓转铁蛋白的热力学结合常数。

Thermodynamic binding constants for gallium transferrin.

作者信息

Harris W R, Pecoraro V L

出版信息

Biochemistry. 1983 Jan 18;22(2):292-9. doi: 10.1021/bi00271a010.

Abstract

Gallium-67 is widely used as an imaging agent for tumors and inflammatory abscesses. It is well established that Ga3+ travels through the circulatory system bound to the serum iron transport protein transferrin and that this protein binding is an essential step in tumor localization. However, there have been conflicting reports on the magnitude of the gallium-transferrin binding constants. Therefore, thermodynamic binding constants for gallium complexation at the two specific metal binding sites of human serum transferrin at pH 7.4 and 5 mM NaHCO3 have been determined by UV difference spectroscopy. The conditional constants calculated for 27 mM NaHCO3 are log K1 = 20.3 and log K2 = 19.3. These results are discussed in relation to the thermodynamics of transferrin binding of Fe3+ and to previous reports on gallium binding. The strength of transferrin complexation is also compared to that of a series of low molecular weight ligands by using calculated pM values (pM = -log [Ga-(H2O)6]) to express the effective binding strength at pH 7.4.

摘要

镓-67被广泛用作肿瘤和炎性脓肿的显像剂。众所周知,Ga3+通过与血清铁转运蛋白转铁蛋白结合在循环系统中运输,并且这种蛋白结合是肿瘤定位的关键步骤。然而,关于镓-转铁蛋白结合常数的大小存在相互矛盾的报道。因此,通过紫外差光谱法测定了在pH 7.4和5 mM NaHCO3条件下,人血清转铁蛋白两个特定金属结合位点上镓络合的热力学结合常数。在27 mM NaHCO3条件下计算得到的条件常数为log K1 = 20.3和log K2 = 19.3。结合Fe3+转铁蛋白结合的热力学以及之前关于镓结合的报道对这些结果进行了讨论。通过计算pM值(pM = -log [Ga-(H2O)6])来表示在pH 7.4时的有效结合强度,还将转铁蛋白络合的强度与一系列低分子量配体的强度进行了比较。

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