首页|重组腺相关病毒感染细胞后目的蛋白表达水平检测方法的建立及验证

重组腺相关病毒感染细胞后目的蛋白表达水平检测方法的建立及验证

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目的 建立重组腺相关病毒(recombinant adeno-associated virus,rAAV)感染细胞后目的蛋白表达水平的检测方法,并进行方法验证,以期用于rAAV9生产过程中不同阶段产物的质量监控.方法 将rAAV9供试品用感染增强剂Envirus-AAV处理后,感染经羟基脲(hydroxyurea,HU)作用的人脑星形胶质母细胞瘤细胞U87-MG,以rAAV9参考品为标准,采用ELISA法检测细胞中目的蛋白戊二酰辅酶A脱氢酶(glutaryl-CoA dehydrogenase,GCDH)的表达水平,并验证方法的专属性、准确性、精密性、线性范围、定量限及耐用性.采用建立的方法检测8批rAAV9供试品.结果 供试品缓冲液的A45.-A63.为0.3,略低于蛋白定量四参数标准曲线最低稀释点(1 ng/mL);150%、100%、50%理论相对效价水平样品平均回收率均在100.0%~107.3%范围内;同1名实验员重复3次及不同实验员检测3个理论相对效价水平样品的目的蛋白表达水平RSD均<25%;rAAV9供试品在50%~150%理论相对效价水平范围内,与相应的目的蛋白表达水平呈良好的线性关系,直线回归方程为y=1.077 x-0.022,R2为0.984;方法的定量限为0.59,即6.0× 1012 vg/mL;U87-MG细胞用HU孵育不同时间(18、21、24 h)、细胞培养上清液于不同条件(室温放置0.5 h、-60 ℃以下放置12 h、-60 ℃以下放置24 h)保存后,目的蛋白表达水平RSD均<25%.1~8批rAAV9供试品目的蛋白表达水平分别为 111%、121%、72%、65%、86%、75%、102%、91%.结论 建立的rAAV感染细胞后目的蛋白表达水平检测方法具有良好的专属性、准确性、精密性及耐用性,可用于rAAV9生产过程中不同阶段产物的质量监控.
Establishment and validation of a method for determination of interesting protein expression level in cells infected with recombinant adeno-associated virus
Objective To establish and validate a method for the determination of the interesting protein expression level of recombinant adeno-associated virus(rAAV)infected cells,so as to monitor the product quality in different stages of rAAV9 production process.Methods After incubation of serial diluted rAAV samples with infection enhancer Envirus-AAV,the human malignant glioblastoma cells(U87-MG)pretreated with hydroxyurea(HU)were infected.Using rAAV9 reference as the standard,the expression level of glutaryl-CoA dehydrogenase(GCDH)was detected by ELISA,and the specificity,accuracy,precision,linear range,limit of quantitation(LOQ)and durability of the method were verified.Eight batches of rAAV9 samples were detected by the established method.Results The A450-A630 value of the sample buffer was 0.3,which was slightly lower than the lowest dilution point(1 ng/mL)of the four-parameter standard curve for protein quantification.The average recoveries of samples with 150%,100%and 50%theoretical relative titer levels were in the range of 100.0%-107.3%.The RSDs of the target protein expression level of the samples with three theoretical relative titer levels detected by the same experimenter three times and different experimenters were all less than 25%.There was a good linear relationship between rAAV9 samples and the target protein expression levels in the range of 50%-150%theoretical relative titer levels,and the linear regression equation was y=1.077 x-0.022,R2=0.984.The LOQ of the method was 0.59,namely 6.0 × 1012 vg/mL.After U87-MG cells were incubated with HU for different time(18,21,24 h),and the culture supernatant was stored under different conditions(room temperature for 0.5 h,below-60 ℃ for 12 h,below-60 ℃ for 24 h).The RSDs of target protein expression levels were all less than 25%.The target protein expression levels of 1-8 batches of rAAV9 samples were 111%,121%,72%,65%,86%,75%,102%and 91%,respectively.Conclusion The established method for the deter-mination of the target protein expression level after rAAV infection has good specificity,accuracy,precision and durability,and can be used for the quality control of products in different stages of rAAV9 production.

Recombinant adeno-associated virus(rAAV)Human malignant glioblastoma cells(U87-MG)Interesting proteinHydroxyurea(HU)Infection enhancerELISA

裴德宁、闫书美、史新昌、胡倩、周勇、刘宾

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中国食品药品检定研究院国家卫生健康委员会生物技术产品检定方法及其标准化重点实验室国家药品监督管理局生物制品质量研究与评价重点实验室,北京 100050

上海泰昶生物技术有限公司,上海 201413

上海天泽云泰生物医药有限公司,上海 201203

重组腺相关病毒 人脑星形胶质母细胞瘤细胞 目的蛋白 羟基脲 感染增强剂 酶联免疫吸附试验

国家重点研发计划中央级公益性科研院所基本科研业务费专项中国医科院项目

2023YFC34033052023-PT350-01

2024

中国生物制品学杂志
中华预防医学会,长春生物制品研究所有限责任公司

中国生物制品学杂志

CSTPCD
影响因子:0.417
ISSN:1004-5503
年,卷(期):2024.37(6)