Eber S W, Morris S A, Schröter W, Gratzer W B
Department of Pediatrics, University of Göttingen, West Germany.
J Clin Invest. 1988 Feb;81(2):523-30. doi: 10.1172/JCI113350.
An abnormal spectrin, in which one subunit is truncated, has been detected in a large German family. The inheritance is autosomal dominant. The affected members of the family suffer in widely varying degree from a microcytic hemolytic anemia. The red cell morphology varies correspondingly from smooth elliptocytes to predominantly poikilocytes. The abnormal spectrin makes up approximately 30% of the total and is almost entirely present as the dimer. The truncated chain is not phosphorylated by the endogenous cAMP-independent kinase, and it has been identified as a chain of beta-type, using monoclonal antibodies. Because a univalent terminal spectrin alpha-chain fragment will bind to normal dimers with an association constant lower by only a factor of two than that for the self-association of the dimers, it would be expected that the mutant dimers (alpha beta') would readily enter into an association with normal (alpha beta) dimers to give alpha 2 beta beta' tetramers (though not with each other). In dilute solution this is indeed observed, and the diminution in tetramer concentration when 30% of normal spectrin is replaced by alpha beta' dimers, amounts to only a small proportion. Moreover, in the membrane skeleton, if there is pairwise apposition of dimer units, only 9% of pairings will be between units that cannot associate. We have shown that the failure of alpha beta' dimers to enter into heterologous associations in situ is not due to the elimination of the ankyrin binding site near the truncated end of the beta-chain: this site is fully functional, as judged by rebinding to spectrin-depleted vesicles. When the spectrin is extracted from the membrane in the cold, the material released initially consists almost entirely of alpha beta' dimers; when the spectrin of normal membranes is partly dissociated to dimers in situ by warming at low ionic strength, extraction in the cold then leads similarly to much more rapid release of the dimer than of the tetramer. The similar rates of liberation of normal and abnormal dimer make it unlikely that the interaction of the latter with the membrane is in any way defective. When mixtures of alpha beta and alpha beta' dimers are bound to spectrin-depleted inside-out membrane vesicles from normal cells and tetramers are allowed to form by equilibration at 30 degrees C, the proportion of the abnormal species appearing in the tetramer is much lower than would be expected on a statistical basis. The relation of the self-association equilibrium on the membrane to that of spectrin in dilute solution is analyzed.
在一个德裔大家族中检测到一种异常血影蛋白,其中一个亚基被截短。其遗传方式为常染色体显性遗传。该家族中受影响的成员患有程度各异的小细胞溶血性贫血。红细胞形态相应地从光滑椭圆形红细胞变化到以异形红细胞为主。异常血影蛋白约占总量的30%,几乎完全以二聚体形式存在。截短的链不能被内源性非cAMP依赖性激酶磷酸化,使用单克隆抗体已鉴定其为β型链。由于单价末端血影蛋白α链片段与正常二聚体结合的缔合常数仅比二聚体自身缔合的缔合常数低两倍,因此预计突变二聚体(αβ')会很容易与正常(αβ)二聚体缔合形成α2ββ'四聚体(尽管它们自身不会缔合)。在稀溶液中确实观察到了这种情况,当30%的正常血影蛋白被αβ'二聚体取代时,四聚体浓度的降低仅占很小的比例。此外,在膜骨架中,如果二聚体单元成对并列,只有9%的配对是在不能缔合的单元之间。我们已经表明,αβ'二聚体在原位不能进行异源缔合并非由于β链截短端附近锚蛋白结合位点的消除:从与血影蛋白耗尽的囊泡重新结合的情况判断,该位点功能完全正常。当在低温下从膜中提取血影蛋白时,最初释放的物质几乎完全由αβ'二聚体组成;当正常膜的血影蛋白在低离子强度下通过升温在原位部分解离为二聚体时,然后在低温下提取同样会导致二聚体比四聚体更快地释放。正常二聚体和异常二聚体相似的释放速率表明,后者与膜的相互作用不太可能存在任何缺陷。当αβ和αβ'二聚体的混合物与来自正常细胞的血影蛋白耗尽的内向外膜囊泡结合,并在30℃平衡以形成四聚体时,出现在四聚体中的异常种类的比例远低于统计学预期。分析了膜上的自缔合平衡与稀溶液中血影蛋白的自缔合平衡之间的关系。