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凝血因子VIII相关蛋白的研究。I. 人凝血因子VIII相关蛋白的超微结构和电泳异质性。

Studies on factor VIII-related protein. I. Ultrastructural and electrophoretic heterogeneity of human factor VIII-related protein.

作者信息

Beck E A, Tranqui-Pouit L, Chapel A, Perret B A, Furlan M, Hudry-Clergeon G, Suscillon M

出版信息

Biochim Biophys Acta. 1979 May 23;578(1):155-63. doi: 10.1016/0005-2795(79)90123-5.

Abstract

Human factor VIII-related protein precipitates with specific heterologous anti-bodies directed against purified factor VIII and supports ristocetin-induced aggregation of washed platelets. We purified human factor VIII from cryoprecipitate by subsequent gel filtration on crosslinked large-pore agarose. Factor VIII-related protein appeared as a large aggregate following electrophoresis on 3% polyacrylamide gels in the presence of sodium dodecyl sulfate (SDS). The same material was separated into multiple bands (molecular weight in excess of several millions) following electrophoresis on SDS-1% agarose gels. After complete disulfide reduction of factor VIII-related protein and electrophoresis on SDS-5% polyacrylamide gels a single subunit chain (Mr approximately equal to 200 000) was revealed. Analysis of this protein, in its non-reduced state, by negative contrast electron microscopy showed filaments of markedly variable size. The calculated molecular weight of such filaments ranged from about 0.6.10(6) to 20.10(6). We conclude that size heterogeneity is an essential feature of human factor VIII-related protein.

摘要

人凝血因子VIII相关蛋白可与针对纯化因子VIII的特异性异源抗体沉淀,并支持瑞斯托霉素诱导的洗涤血小板聚集。我们通过在交联大孔琼脂糖上进行凝胶过滤,从冷沉淀中纯化人凝血因子VIII。在十二烷基硫酸钠(SDS)存在下,于3%聚丙烯酰胺凝胶上进行电泳后,凝血因子VIII相关蛋白呈现为大的聚集体。在SDS - 1%琼脂糖凝胶上进行电泳后,相同物质被分离成多条带(分子量超过数百万)。在凝血因子VIII相关蛋白完全二硫键还原并在SDS - 5%聚丙烯酰胺凝胶上进行电泳后,显示出一条单亚基链(Mr约等于200 000)。通过负染色电子显微镜对处于非还原状态的该蛋白进行分析,显示出大小明显不同的细丝。这种细丝的计算分子量范围约为0.6×10⁶至20×10⁶。我们得出结论,大小异质性是人凝血因子VIII相关蛋白的一个基本特征。

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