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对带3孟菲斯变体II(Pro-854→Leu)上芪二磺酸盐结合位点的表征。

Characterization of the stilbenedisulphonate binding site on band 3 Memphis variant II (Pro-854-->Leu).

作者信息

Salhany J M, Sloan R L, Schopfer L M

机构信息

Veterans Administration Medical Center, Omaha, NE, USA.

出版信息

Biochem J. 1996 Jul 15;317 ( Pt 2)(Pt 2):509-14. doi: 10.1042/bj3170509.

Abstract

Band 3 Memphis variant II is a mutant anion-exchange protein associated with the Diego a+ blood group antigen. There are two mutations in this transporter: Lys-56-->Glu within the cytoplasmic domain, and Pro-854-->Leu within the membrane-bound domain. The Pro-854 mutation, which is thought to give rise to the antigenicity, is located within the C-terminal subdomain of the membrane-bound domain. Yet, there is an apparent enhancement in the rate of covalent binding of H2DIDS (4,4'-di-isothiocyanatodihydro-2, 2'-stilbenedisulphonate) to 'lysine A' (Lys-539) in the N-terminal subdomain, suggesting widespread conformational changes. In this report, we have used various kinetic assays which differentiate between conformational changes in the two subdomains, to characterize the stilbenedisulphonate site on band 3 Memphis variant II. We have found a significantly higher H2DIDS (a C-terminal-sensitive inhibitor) affinity for band 3 Memphis variant II, due to a lower H2DIDS 'off' rate constant, but no difference was found between mutant and control when DBDS (4,4'-dibenzamido-2,2'-stilbenedisulphonate) (a C-terminal-insensitive inhibitor) 'off' rates were measured. Furthermore, there were no differences in the rates of covalent binding to lysine A, for either DIDS (4,4'-di-isothiocyanato-2,2'-stilbenedisulphonate) or H2DIDS. However, the rate of covalent intrasubunit cross-linking of Lys-539 and Lys-851 by H2DIDS was abnormally low for band 3 Memphis variant II. These results suggest that the Pro-854-->Leu mutation causes a localized conformational change in the C-terminal subdomain of band 3.

摘要

3型孟菲斯变体II是一种与迭戈a+血型抗原相关的突变阴离子交换蛋白。该转运蛋白存在两个突变:细胞质结构域内的赖氨酸-56突变为谷氨酸,膜结合结构域内的脯氨酸-854突变为亮氨酸。被认为产生抗原性的脯氨酸-854突变位于膜结合结构域的C末端亚结构域内。然而,在N末端亚结构域中,4,4'-二异硫氰酸二氢-2,2'-二苯乙烯二磺酸盐(H2DIDS)与“赖氨酸A”(赖氨酸-539)的共价结合速率明显增强,这表明存在广泛的构象变化。在本报告中,我们使用了各种动力学分析方法来区分两个亚结构域的构象变化,以表征3型孟菲斯变体II上的二苯乙烯二磺酸盐位点。我们发现,由于H2DIDS的“解离”速率常数较低,3型孟菲斯变体II对H2DIDS(一种C末端敏感抑制剂)的亲和力显著更高,但在测量4,4'-二苯甲酰胺基-2,2'-二苯乙烯二磺酸盐(DBDS,一种C末端不敏感抑制剂)的“解离”速率时,突变体与对照之间没有差异。此外,对于4,4'-二异硫氰酸-2,2'-二苯乙烯二磺酸盐(DIDS)或H2DIDS,与赖氨酸A的共价结合速率没有差异。然而,对于3型孟菲斯变体II,H2DIDS导致的赖氨酸-539和赖氨酸-851的亚基内共价交联速率异常低。这些结果表明,脯氨酸-854突变为亮氨酸会导致3型蛋白C末端亚结构域发生局部构象变化。

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