罗素蛇毒因子X激活剂快速制备凝血酶的最佳条件研究

Narin Kijkriengkraikul, I. Nuchprayoon
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引用次数: 0

摘要

本研究的目的是探索一种简单的方法和最佳条件,在此过程中使用RVV-X快速制备冷沉淀耗尽血浆(CDP)凝血酶。研究了从人CDP制备凝血酶的不同因素,包括:1)RVV-X;2)氯化钙溶液体积;3)最终提取氯化钠溶液的体积;4)潜伏期。用凯氏定氮法测定纤维蛋白凝块形成、总蛋白,用SDS-PAGE法测定凝血酶时间、分子量和蛋白谱,用凝血分析仪测定凝血酶浓度。介绍了凝血酶的制备方法和工艺,以及以CDP为起始原料100 ml快速制备最高收率凝血酶的最佳工艺条件的研究。得出四种最佳条件:1)rvv - x50 mcg;2) 0.25 M氯化钙的体积应为3ml;3) 0.85%氯化钠用于最终蛋白沉淀提取的体积应为10 ml;4)凝血酶原活化过程无需孵育时间。在最佳条件下制备的溶液在SDS-PAGE上显示出明显的条带,分子量约为36,000 Da,这是我们的目标蛋白凝血酶。制备的溶液总蛋白含量为0.065 g/dl,凝血酶时间(9秒)和纤维蛋白凝块形成结果令人满意。实验结果表明,该方法加孵育前后凝血酶浓度分别为269.4和295.2 IU/ml。结果表明,不经凝血酶原活化的RVV-X法(最佳条件)凝血酶产率最高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Study of Optimum Condition for Rapid Preparation of Thrombin using Russell’s Viper Venom Factor X Activator
The purpose of this study is to investigate a simple method with the optimum condition for rapid thrombin preparation from Cryoprecipitate-depleted Plasma (CDP) using RVV-X in the process. Thrombin preparation from human CDP was studied with the presence of different factors in batch condition including: 1) RVV-X; 2) volume of calcium chloride solution; 3) volume of sodium chloride solution for final extraction; and 4) incubation time. The properties of the prepared sample were analyzed for fibrin clot formation, total protein by Kjeldahl method, thrombin time, molecular weight and protein patterns by SDS-PAGE, and thrombin concentration by coagulation analyzer. The method and process of preparing thrombin and the study of optimum condition for rapidly preparing the highest yield of thrombin from starting CDP 100 ml were introduced. The best four conditions were concluded: 1) RVV-X 50 mcg should be present in the process; 2) volume of 0.25 M calcium chloride should be 3 ml; 3) volume of 0.85% sodium chloride for the final protein precipitate extraction should be 10 ml and; 4) no incubation time needed for prothrombin activation process. A solution prepared from the optimum condition showed an obvious band on SDS-PAGE at a molecular weight about 36,000 Da which is our target protein thrombin. The prepared solution had a total protein content of 0.065 g/dl and gave satisfactory results of thrombin time (9 seconds) and fibrin clot formation. The test results of thrombin concentration between the method with and without incubation time were 269.4 and 295.2 IU/ml, respectively. This result showed that the method with RVV-X but without incubation time for prothrombin activation (optimum condition) gave the highest yield of thrombin.
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