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作 者:肖兰艳 何颖[1] 刘雪婷[1] 邹泽红[1] 陈惠芳[1] 李碧舟 及志恒 陶爱林[1]
机构地区:[1]广州医科大学附属第二医院,广东省过敏反应与免疫重点实验室/呼吸疾病国家重点实验室变态反应研究室,广东广州510260
出 处:《热带医学杂志》2015年第5期583-586,共4页Journal of Tropical Medicine
基 金:国家科技重大专项重点课题(2014ZX08011-005B);国家临床重点专科建设项目(520102);广州市科技攻关项目(201300000159)
摘 要:目的去除重组巴西坚果过敏原蛋白Ber e 1(r Ber e 1)溶液中的内毒素,为后续实验和重组过敏原蛋白的临床应用打下基础。方法采用亲和层析法、超滤法和离子交换法联合应用以及Triton X-114萃取法与亲和层析法联合应用,比较这两个方案去除重组蛋白溶液中的内毒素效果。结果亲和层析法、超滤法和离子交换法联合应用的内毒素去除率为99.99%,内毒素浓度为6.25 EU/ml,蛋白回收率为42.8%;Triton X-114萃取法与亲和层析法联合应用的内毒素去除率为99.99%,内毒素浓度为2.09 EU/ml,蛋白回收率为26.1%。结论 Triton X-114萃取法与亲和层析法联合应用蛋白溶液内毒素的去除效果较佳,且内毒素含量以及Triton X-114残留量均在《中国药典》的规定范围内。Objective To remove the endotoxin from the recombinant protein solution of Brazil nut allergen Ber e 1 to facilitate the further experimental and clinical application. Methods Two purification pathways, the combination of affinity chromatography, ultrafiltration and ion exchange chromatography, and joint applications of Triton X-l14 phase separation and affinity chromatography, were adopted to remove the endotoxin from protein solution. Results Both pathways worked well but with different efficiency. Removal rate of endotoxin was 99.99% and endotoxin level was 6.35 EU / ml with the protein recovery rate of 42.8% after affinity chromatography combined with ultrafiltration and ionexchange chromatography method. After going through Triton X-l14 phase separation and affinity chromatography method,the removal rate of endotoxin was also 99.99%, and the endotoxin concentration could be reduced to 2.09 EU / m L, with the recovery rate of 26.1%. Conclusion Triton X-114 phase separation combined with affinity chromatography method is a better method to purify the recombinant proteins and remove endotoxin. Both endotoxin and Triton X-114 residues in the purified recombinant protein are well below the required limits of Chinese Pharmacopoeia.
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