从人血清中分离硫氧还蛋白的研究

Luay A. Al-Helaly, Amera A. Hamdon
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摘要

本研究包括使用不同的生化技术从人血清中分离硫氧还蛋白(Trx)。透析后硫酸铵沉淀(65%)产生的一个蛋白峰通过凝胶过滤分离出来。用离子交换型deae -纤维素作为凝胶过滤柱的产物,有两个Trx峰。凝胶过滤层析(G-50)和SDS-PAGE电泳技术分离得到的Trx约分子量分别为(12305 + 190)道尔顿和12461道尔顿。结果表明,药物对Trx具有抑制和活化作用。结果表明,对乙酰氨基酚、地沙马松、苯海拉明、无水茶碱、伪麻黄碱、神经酰胺和无水咖啡因的抑制率为44.59%,甲硝唑和苹果酸氯苯那敏的抑制率分别为110.8%和21.62%。
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Study of Thioredoxin Isolated from Human Blood Serum
The research included the separation of thioredoxin (Trx) from human blood serum using different biochemical techniques. One proteinous peak had been isolated by gel filtration using sephadex )G-50) that produced by ammonium sulphate precipitation(65%) after dialysis.  It was noted that there are two peaks of Trx when using ion exchange-type DEAE-cellulose for the product of gel filtration column. The approximately molecular weight of the isolated Trx using gel filtration chromatography (G-50) and electrophoresis technique type SDS-PAGE were (12305 + 190) Dalton and 12461 Dalton respectively . The results showed that inhibited and activated effects of drugs on Trx working. The results showed that inhibited to 44.59% for paracetamol, dexathamazone, diphenhydramine-HCl, theophlline anhydrous,  pseudoephedrine, ceramide and caffeine anhydrous, but metronidazole and chlorpheniramine malate have activated effect to 110.8% and 21.62 respectively. 
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