al Yacoub Nadya, Romanowska Malgorzata, Haritonova Natalie, Foerster John
Department of Dermatology, Charité University Hospital, Berlin, Germany.
J Gene Med. 2007 Jul;9(7):579-84. doi: 10.1002/jgm.1052.
Generation of high titer lentiviral stocks and efficient virus concentration are central to maximize the utility of lentiviral technology. Here we evaluate published protocols for lentivirus production on a range of transfer vectors differing in size (7.5-13.2 kb). We present a modified virus production protocol robustly yielding useful titers (up to 10(7)/ml) for a range of different transfer vectors containing packaging inserts up to 7.5 kb. Moreover, we find that virus recovery after concentration by ultracentrifugation depends on the size of the packaged inserts, heavily decreasing for large packaged inserts. We describe a fast (4 h) centrifugation protocol at reduced speed allowing high virus recovery even for large and fragile lentivirus vectors. The protocols outlined in the current report should be useful for many labs interested in producing and concentrating high titer lentiviral stocks.
产生高滴度慢病毒储备液以及高效浓缩病毒对于最大化慢病毒技术的效用至关重要。在此,我们评估了已发表的关于在一系列大小不同(7.5 - 13.2 kb)的转移载体上生产慢病毒的方案。我们提出了一种改良的病毒生产方案,对于一系列包含长达7.5 kb包装插入片段的不同转移载体,能稳健地产生有用的滴度(高达10⁷/ml)。此外,我们发现超速离心浓缩后的病毒回收率取决于包装插入片段的大小,对于大的包装插入片段,回收率会大幅降低。我们描述了一种快速(4小时)的低速离心方案,即使对于大的和易碎的慢病毒载体也能实现高病毒回收率。本报告中概述的方案对于许多有兴趣生产和浓缩高滴度慢病毒储备液的实验室应该是有用的。