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东南亚椭圆形红细胞增多症中突变带3对正常带3结构的显性作用的分子基础及功能后果

Molecular basis and functional consequences of the dominant effects of the mutant band 3 on the structure of normal band 3 in Southeast Asian ovalocytosis.

作者信息

Kuma Hiroyuki, Abe Yoshito, Askin David, Bruce Lesley J, Hamasaki Tomohiro, Tanner Michael J A, Hamasaki Naotaka

机构信息

Department of Clinical Chemistry and Laboratory Medicine, Graduate School of Medical Sciences, Kyushu University, Fukuoka 812-8582, Japan.

出版信息

Biochemistry. 2002 Mar 12;41(10):3311-20. doi: 10.1021/bi011678+.

Abstract

Southeast Asian ovalocytosis (SAO) human red cell membranes contain similar proportions of normal band 3 and a mutant band 3 with a nine amino acid deletion (band 3 SAO). We employed specific chemical modification and proteolytic cleavage to probe the structures of band 3 in normal and SAO membranes. When the membranes were modified specifically at lysine residues with N-hydroxysulfosuccinimide-SS-biotin, band 3 Lys-851 was not modified in normal membranes but quantitatively modified in SAO membranes. Normal and SAO membranes showed different patterns of band 3 proteolytic cleavage. Notably, many sites cleaved in normal membranes were not cleaved in SAO membranes, despite the presence of normal band 3 in these membranes. The mutant band 3 changes the structure of essentially all the normal band 3 present in the SAO membranes, and these changes extend throughout the normal band 3 molecules. The results also imply that band 3 in SAO membranes is present as hetero-tetramers or higher hetero-oligomers. The dominant structural effects of band 3 SAO on the other band 3 allele have important consequences on the functional and hematological properties of human red cells heterozygous for band 3 SAO. Analysis of the altered profile of biotinylation and protease cleavage sites suggests the location of exposed surfaces in the band 3 membrane domain and identifies likely interacting regions within the molecule. Our approach provides a sensitive method for studying structural changes in polytopic membrane proteins.

摘要

东南亚椭圆形红细胞增多症(SAO)患者的红细胞膜中,正常带3和缺失九个氨基酸的突变带3(带3 SAO)的比例相似。我们采用特定的化学修饰和蛋白水解切割来探究正常膜和SAO膜中带3的结构。当用N-羟基琥珀酰亚胺-SS-生物素对赖氨酸残基进行特异性修饰时,正常膜中的带3 Lys-851未被修饰,而SAO膜中的带3 Lys-851被定量修饰。正常膜和SAO膜显示出不同的带3蛋白水解切割模式。值得注意的是,尽管这些膜中存在正常带3,但正常膜中许多被切割的位点在SAO膜中并未被切割。突变的带3改变了SAO膜中几乎所有正常带3的结构,并且这些变化延伸至整个正常带3分子。结果还表明,SAO膜中的带3以异源四聚体或更高的异源寡聚体形式存在。带3 SAO对另一个带3等位基因的主要结构效应,对携带带3 SAO的杂合人类红细胞的功能和血液学特性具有重要影响。对生物素化和蛋白酶切割位点改变图谱的分析表明了带3膜结构域中暴露表面的位置,并确定了分子内可能的相互作用区域。我们的方法为研究多跨膜蛋白的结构变化提供了一种灵敏的方法。

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