Galliano M, Minchiotti L, Iadarola P, Zapponi M C, Ferri G, Castellani A A
J Biol Chem. 1986 Mar 25;261(9):4283-7.
Mutant forms of human serum albumin have been detected on the basis of their abnormal electrophoretic mobility which is either faster or slower than that of normal albumin. In the present work we have studied the structure of a slow variant, referred to as albumin Ge/Ct, in order to define the cause of its genetic abnormality. The protein was isolated from the serum of a young healthy woman homozygous for the variant. Analysis of CNBr fragments by isoelectric focusing allowed us to localize the mutation to the COOH-terminal region of the molecule (residues 549-585). This fragment was isolated on a preparative scale and subjected to tryptic digestion. All tryptic peptides were purified by reverse-phase high performance liquid chromatography and characterized. Sequential analysis of three abnormal peptides revealed that albumin Ge/Ct has a shortened chain with the following COOH-terminal sequence: Leu-Val-Ala-Ala-Ser-Lys580-Leu-Pro. The presence of an additional lysine residue accounts for the electrophoretic behavior of the variant. It is likely that the variant may be caused by a single base deletion in the structural gene, a Cyt in mRNA codon 580, and the consequent shift in reading frame.
已根据其异常的电泳迁移率检测到人类血清白蛋白的突变形式,其迁移率比正常白蛋白快或慢。在本研究中,我们研究了一种慢变体(称为白蛋白Ge/Ct)的结构,以确定其遗传异常的原因。该蛋白质是从一名该变体纯合子的年轻健康女性血清中分离出来的。通过等电聚焦分析CNBr片段,使我们能够将突变定位到分子的COOH末端区域(残基549 - 585)。该片段在制备规模上分离出来并进行胰蛋白酶消化。所有胰蛋白酶肽段通过反相高效液相色谱法纯化并进行表征。对三个异常肽段的序列分析表明,白蛋白Ge/Ct有一条缩短的链,其COOH末端序列如下:Leu-Val-Ala-Ala-Ser-Lys580-Leu-Pro。额外赖氨酸残基的存在解释了该变体的电泳行为。该变体可能是由结构基因中的单个碱基缺失(mRNA密码子580中的一个Cyt)以及随之而来的阅读框移位引起的。