Suppr超能文献

消除慢病毒载体生产中生产细胞的 retro-transduction。

Abolishing Retro-Transduction of Producer Cells in Lentiviral Vector Manufacturing.

机构信息

VIVEbiotech, Tandem Building, 20014 Donostia, Spain.

出版信息

Viruses. 2024 Jul 29;16(8):1216. doi: 10.3390/v16081216.

Abstract

Transduction of producer cells during lentiviral vector (LVV) production causes the loss of 70-90% of viable particles. This process is called retro-transduction and it is a consequence of the interaction between the LVV envelope protein, VSV-G, and the LDL receptor located on the producer cell membrane, allowing lentiviral vector transduction. Avoiding retro-transduction in LVV manufacturing is crucial to improve net production and, therefore, the efficiency of the production process. Here, we describe a method for quantifying the transduction of producer cells and three different strategies that, focused on the interaction between VSV-G and the LDLR, aim to reduce retro-transduction.

摘要

在慢病毒载体 (LVV) 生产过程中,生产细胞的转导会导致 70-90%的有活力颗粒丢失。这个过程称为 retro-transduction,是 LVV 包膜蛋白 VSV-G 与位于生产细胞膜上的 LDL 受体相互作用的结果,允许慢病毒载体转导。在 LVV 制造中避免 retro-transduction 对于提高净产量至关重要,因此也能提高生产过程的效率。在这里,我们描述了一种定量分析生产细胞转导的方法和三种不同的策略,这些策略集中在 VSV-G 和 LDLR 之间的相互作用上,旨在减少 retro-transduction。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cfd/11359676/425ae9392222/viruses-16-01216-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验