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患有遗传性椭圆形红细胞增多症的黑人患者中一种新的异常血影蛋白变体。

A new abnormal variant of spectrin in black patients with hereditary elliptocytosis.

作者信息

Lecomte M C, Dhermy D, Solis C, Ester A, Féo C, Gautero H, Bournier O, Boivin P

出版信息

Blood. 1985 May;65(5):1208-17.

PMID:3922449
Abstract

Seven black patients with mild hereditary elliptocytosis (HE) from five unrelated families were studied. The erythrocytes of these patients exhibited an abnormal thermal sensitivity (between 45 degrees C and 47 degrees C instead of 49 degrees C). An important defect of spectrin dimer self-association was detected in two ways: (1) the proportions of spectrin dimer (SpD) extracted from membranes at 4 degrees C under low ionic strength conditions were increased between 25% and 56% (normal value 15% +/- 2%); (2) the spectrin dimer----tetramer conversion in solution were defective with an association constant value between 0.4 and 2.4 X 10(5) M-1 for a normal value of 6 +/- 0.4 X 10(5) M-1. Spectrin (Sp) from HE patients and normal volunteers (32 black and 22 white subjects) was submitted to limited tryptic digestion, followed by one- or two-dimensional separation of the peptides. Peptide patterns of crude Sp from all seven HE patients exhibited a marked and reproducible decrease in 80,000-dalton peptide (previously identified as the dimer-dimer interaction domain of the alpha-chain) and a concomitant appearance of a novel 65,000-dalton peptide. A minor fragment at 28,000 daltons was also decreased. Tryptic digestion of HE spectrin dimer and tetramer (SpT), isolated after the SpD self-association procedure in solution, revealed modifications (decrease in the 80,000-dalton peptide and presence of a 65,000-dalton peptide) predominantly in HE SpD when peptide patterns of HE SpT were quite similar to control SpT patterns. Immunoblots with anti-alpha-chain antibodies revealed that the 65,000-dalton peptide derived from the alpha-chain. Kinetic studies of Sp digestion showed that the 65,000-dalton peptide did not result from further digestion of a 74,000 intermediate and was not a precursor of 46,000- to 50,000-dalton peptides. These results show a new structural defect of Sp-alpha-chain, associated with a defective Sp dimer self-association in HE.

摘要

对来自五个无亲缘关系家庭的七名患有轻度遗传性椭圆形红细胞增多症(HE)的黑人患者进行了研究。这些患者的红细胞表现出异常的热敏感性(在45摄氏度至47摄氏度之间,而非49摄氏度)。通过两种方式检测到血影蛋白二聚体自缔合存在重要缺陷:(1)在低离子强度条件下于4摄氏度从膜中提取的血影蛋白二聚体(SpD)比例增加了25%至56%(正常值为15%±2%);(2)溶液中的血影蛋白二聚体向四聚体的转化存在缺陷,缔合常数在0.4至2.4×10⁵ M⁻¹之间,而正常值为6±0.4×10⁵ M⁻¹。对HE患者和正常志愿者(32名黑人及22名白人受试者)的血影蛋白(Sp)进行有限胰蛋白酶消化,随后对肽段进行一维或二维分离。所有七名HE患者的粗Sp肽图谱显示,80,000道尔顿肽段(先前鉴定为α链的二聚体 - 二聚体相互作用结构域)明显且可重复地减少,同时出现一种新的65,000道尔顿肽段。28,000道尔顿的一个小片段也减少了。对在溶液中进行SpD自缔合程序后分离得到的HE血影蛋白二聚体和四聚体(SpT)进行胰蛋白酶消化,结果显示,当HE SpT的肽图谱与对照SpT图谱相当相似时,修饰(80,000道尔顿肽段减少以及65,000道尔顿肽段的存在)主要出现在HE SpD中。用抗α链抗体进行免疫印迹显示,65,000道尔顿肽段源自α链。Sp消化的动力学研究表明,65,000道尔顿肽段不是由74,000中间体的进一步消化产生的,也不是46,000至50,000道尔顿肽段的前体。这些结果显示了Sp - α链的一种新的结构缺陷,与HE中存在缺陷的Sp二聚体自缔合相关。

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