电穿孔
转染
细胞生物学
嵌合抗原受体
抗原
背景(考古学)
生物
信使核糖核酸
抗原提呈细胞
MHC I级
主要组织相容性复合体
细胞培养
计算生物学
T细胞
免疫学
免疫系统
遗传学
基因
古生物学
作者
Tatjana Sauerer,Leoni Albrecht,Nico M. Sievers,Kerstin F. Gerer,Stefanie Hoyer,Jan Dörrie,Niels Schaft
出处
期刊:Methods in molecular biology
日期:2024-01-01
卷期号:: 219-235
标识
DOI:10.1007/978-1-0716-3770-8_10
摘要
Electroporation (EP) of mRNA into human cells is a broadly applicable method to transiently express proteins of choice in a variety of different cell types. We have spent more than two decades to optimize and adapt this method, first for antigen-loading of dendritic cells (DCs) and subsequently for T cells, B cells, bulk PBMCs, and several cell lines. In this regard, antigens were introduced, processed, and presented in context of MHC class I and II. Next to that, functional proteins like adhesion receptors, T-cell receptors (TCRs), chimeric antigen receptors (CARs), constitutively active signal transducers (i.e. caIKK), and others were successfully expressed. We have also established this protocol under full GMP compliance as part of a manufacturing license to produce mRNA-electroporated DCs and mRNA-electroporated T cells for therapeutic applications in clinical trials. Therefore, we here want to share our universal mRNA electroporation protocol and the experience we have gathered with this method. The advantages of the transfection method presented here are: (1) easy adaptation to different cell types; (2) scalability from 10
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