Development of an HEK293 Suspension Cell Culture Medium, Transient Transfection Optimization Workflow, and Analytics for Batch rAAV Manufacturing

转染 效价 HEK 293细胞 细胞培养 生物制造 瞬态(计算机编程) 病毒载体 计算机科学 计算生物学 纳米技术 生物技术 化学 重组DNA 生物 病毒 材料科学 病毒学 遗传学 基因 生物化学 操作系统
作者
Erica A. Green,Qiang Fu,Nelson Ndhairo,Thomas M Leibiger,Yongdan Wang,Yong-Suk Lee,Kelvin H. Lee,Michael J. Betenbaugh,Seongkyu Yoon,David J. McNally
出处
期刊:Biotechnology and Bioengineering [Wiley]
卷期号:122 (7): 1640-1655 被引量:2
标识
DOI:10.1002/bit.28980
摘要

ABSTRACT Recombinant adeno associated virus (rAAV) vectors have become popular delivery vehicles for in vivo gene therapies, but demand for rAAVs continues to outpace supply. Platform processes for rAAV production are being developed by many manufacturers, and transient chemical transfection of human embryonic kidney 293 (HEK293) cells is currently the most popular approach. However, the cutting edge nature of rAAV process development encourages manufacturers to keep cell culture media formulations, plasmid sequences, and other details proprietary, which creates hurdles for small companies and academic labs seeking to innovate in this space. To address this problem, we leveraged the resources of an academic‐industry consortium (Advanced Mammalian Biomanufacturing Innovation Center, AMBIC) to develop an rAAV production system based on transient transfection of suspension HEK293 cells adapted to an in‐house, chemically defined medium. We found that balancing iron and calcium levels in the medium were crucial for maintaining transfection efficiency and minimizing cell aggregation, respectively. A design of experiments approach was used to optimize the transient transfection process for batch rAAV production, and PEI:DNA ratio and cell density at transfection were the parameters with the strongest effects on vector genome (VG) titer. When the optimized transient process was transferred between two university sites, VG titers were within a twofold range. Analytical characterization showed that purified rAAV from the AMBIC process had comparable viral protein molecular weights versus vector derived from commercial processes, but differences in transducing unit (TU) titer were observed between vector preps. The developed media formulation, transient transfection process, and analytics for VG titer, capsid identity, and TU titer constitute a set of workflows that can be adopted by others to study fundamental problems that could improve product yield and quality in the nascent field of rAAV manufacturing.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
wyz真的帅发布了新的文献求助10
1秒前
望江南子发布了新的文献求助10
1秒前
2秒前
拼搏之柔完成签到 ,获得积分10
2秒前
yy完成签到,获得积分10
3秒前
3秒前
4秒前
小二郎应助猪猪hero采纳,获得10
5秒前
Rencal完成签到 ,获得积分10
8秒前
9秒前
9秒前
9秒前
风中的非笑完成签到 ,获得积分10
10秒前
10秒前
ldx完成签到,获得积分10
10秒前
adieu发布了新的文献求助30
12秒前
Yikepp完成签到,获得积分10
12秒前
wurao完成签到,获得积分10
14秒前
15秒前
在水一方应助砥砺前行采纳,获得10
15秒前
16秒前
希望天下0贩的0应助小炊采纳,获得10
17秒前
林晴晴发布了新的文献求助10
17秒前
17秒前
西风漂流完成签到,获得积分10
18秒前
英姑应助aaa采纳,获得10
20秒前
嘛吉发布了新的文献求助10
20秒前
香云完成签到,获得积分10
20秒前
21秒前
鱼蛋发布了新的文献求助10
21秒前
今后应助Sunyidan采纳,获得10
22秒前
22秒前
tutu完成签到,获得积分10
22秒前
桐桐应助大眼的平松采纳,获得10
25秒前
猪坚强发布了新的文献求助10
25秒前
猪猪hero发布了新的文献求助10
25秒前
tiantian8715完成签到,获得积分10
26秒前
26秒前
光坠星海完成签到 ,获得积分10
27秒前
28秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Les Mantodea de Guyane Insecta, Polyneoptera 2000
Leading Academic-Practice Partnerships in Nursing and Healthcare: A Paradigm for Change 800
Signals, Systems, and Signal Processing 610
Research Methods for Business: A Skill Building Approach, 9th Edition 500
Research Methods for Applied Linguistics 500
Picture Books with Same-sex Parented Families Unintentional Censorship 444
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 物理 内科学 复合材料 催化作用 物理化学 光电子学 电极 细胞生物学 基因 无机化学
热门帖子
关注 科研通微信公众号,转发送积分 6412922
求助须知:如何正确求助?哪些是违规求助? 8231931
关于积分的说明 17472386
捐赠科研通 5465653
什么是DOI,文献DOI怎么找? 2887836
邀请新用户注册赠送积分活动 1864584
关于科研通互助平台的介绍 1703034