首页 | 本学科首页   官方微博 | 高级检索  
检索        

EB病毒特异性DNA酶的纯化制备
引用本文:李泽卿,田勇泉,肖健云,赵素萍,陶正德.EB病毒特异性DNA酶的纯化制备[J].中国耳鼻咽喉颅底外科杂志,2000,6(1):28-31.
作者姓名:李泽卿  田勇泉  肖健云  赵素萍  陶正德
作者单位:1. 南京军区南京总医院耳鼻咽喉科,江苏南京 210002
2. 湖南医科大学附属湘雅医院耳鼻咽喉科,湖南长沙 410008
摘    要:目的 纯化EB病毒特异性DNA酶(EBV-DNase)为鼻咽癌血清学诊断方法-血清EBV-DNase抗体的检测奠定基础。方法 采用多重纤维素柱层析对用联合化学诱导的方法制备的EBV-DNase粗提物进行纯化。 结果 在SDS-PAGE检测中,从粗提物到纯化终产物,蛋白质带逐渐减少直至单一条带。其分子量为52kD,其对应的每豪克蛋白质酶单位分别为5.46,49.19,134.86,391,25,96

关 键 词:DEAE纤维  EBV-DNase  DNA酶  鼻咽肿瘤
文章编号:1007-1520(2000)01-0028-04
修稿时间:1999年8月14日

Pupification of Epstein-Barr virus-specific DNase
LI Ze qing,TIAN Yong quan,XIAO Jian yun,et al..Pupification of Epstein-Barr virus-specific DNase[J].Chinese Journal of Otorhinolaryngology-skull Base Surgery,2000,6(1):28-31.
Authors:LI Ze qing  TIAN Yong quan  XIAO Jian yun  
Abstract:Objective To purify Epstein-Barr virus-specific DNase (EBV-DNase) for further establishment of detection of EBV-DNase antibody in nasopharyngeal carcinoma (NPC) sera. Methods The EBV-DNase extract obtained through combined chemical induction was purified with multistage of gradient linear cellulose column chromatography. Results SDS-PAGE showed that the protein bands were gradually decreased to a single one with a molecular weight of 52kD from the crude extract to the terminal purified product. The immunoradiological determination showed that the units per milligram protein (U/mg) were 5.46, 49.19, 134.86, 391.25 and 967.78 respectively. The enzyme activity was enhanced by 177.2 folds. Conclusion Gradient linear cellulose column chromatography can satisfactorily purify EBV-DNase from the crude cellular extract.
Keywords:EBV-DNase/isol  NASOPHARYNGEAL NEOPLASMS/diag  CHROMATOGRAPHY  DEAE-CELLULOSE
本文献已被 CNKI 维普 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号