Suppr超能文献

凝血因子 VIII 复合物的纯化。

Purification of the factor VIII complex.

作者信息

Thorell L, Blombäck B

出版信息

Thromb Res. 1984 Aug 15;35(4):431-50. doi: 10.1016/0049-3848(84)90235-4.

Abstract

Two high purity factor VIII concentrates, type I and type II were developed for clinical trials in patients with hemophilia A and von Willebrand's disease. Fresh frozen plasma containing 1% polyethylene glycol 4000 was thawed to form cryoprecipitate, which was subsequently dissolved in citrate buffer. By addition of glycine buffer to a final concentration of 2.0 M at 26 degrees C, the bulk of fibrinogen was precipitated while factor VIII remained in solution. Factor VIII was precipitated from the glycine supernatant by addition of solid sodium chloride. The recovery of factor VIII procoagulant activity (VIII:C) per kg plasma was 271 +/- 23 units (n = 4) and 386 +/- 47 units (n = 7) for the type I and the type II preparations, respectively, while the recovery of von Willebrand factor related activity (ristocetin cofactor, VIIIR:RC) was 518 +/- 75 units and 718 +/- 90 units per kg plasma, respectively. The specific activity (units per mg protein) of VIII:C in the type I and type II preparations were 2.53 +/- 1.02 and 7.56 +/- 1.33, respectively. The specific activity (units per mg protein) of VIIIR:RC for the type I and type II preparations were 4.86 +/- 2.32 and 13.6 +/- 3.7, respectively. VIIIR:Ag was present as multimers in both preparations, and the multimeric pattern was similar to that of normal plasma. The preparations have the ability to correct the prolonged bleeding time in severe von Willebrand's disease. The factor VIII complex in the type II preparations was further purified by gel filtration on Sephacryl S-1000. This preparation was free of fibrinogen and fibronectin. Its specific activity in terms of VIII:C was 47 u/mg protein and 104 u/mg protein in terms of VIIIR:RC. The subunit of reduced factor VIIIR:Ag had Mr of 210 Kd on sodium dodecyl sulfate polyacrylamide gel electrophoresis.

摘要

为了对甲型血友病和血管性血友病患者进行临床试验,研发了两种高纯度的VIII因子浓缩剂,即I型和II型。将含有1%聚乙二醇4000的新鲜冰冻血浆解冻形成冷沉淀,随后将其溶解在枸橼酸盐缓冲液中。在26℃下加入甘氨酸缓冲液至最终浓度为2.0M,大部分纤维蛋白原沉淀,而VIII因子仍留在溶液中。通过加入固体氯化钠从甘氨酸上清液中沉淀出VIII因子。I型和II型制剂每千克血浆中VIII因子促凝活性(VIII:C)的回收率分别为271±23单位(n = 4)和386±47单位(n = 7),而血管性血友病因子相关活性(瑞斯托霉素辅因子,VIIIR:RC)的回收率分别为每千克血浆518±75单位和718±90单位。I型和II型制剂中VIII:C的比活性(每毫克蛋白质的单位数)分别为2.53±1.02和7.56±1.33。I型和II型制剂中VIIIR:RC的比活性(每毫克蛋白质的单位数)分别为4.86±2.32和13.6±3.7。两种制剂中VIIIR:Ag均以多聚体形式存在,且多聚体模式与正常血浆相似。这些制剂能够纠正重度血管性血友病患者延长的出血时间。II型制剂中的VIII因子复合物通过在Sephacryl S - 1000上进行凝胶过滤进一步纯化。该制剂不含纤维蛋白原和纤连蛋白。其VIII:C的比活性为47单位/毫克蛋白质,VIIIR:RC的比活性为104单位/毫克蛋白质。在十二烷基硫酸钠聚丙烯酰胺凝胶电泳上,还原后的VIIIR:Ag亚基的分子量为210Kd。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验