Department of Medical Microbiology and Immunology, Creighton University School of Medicine, Omaha, NE 68178, USA.
J Virol Methods. 2011 Jan;171(1):299-302. doi: 10.1016/j.jviromet.2010.11.005. Epub 2010 Nov 16.
Previous work demonstrated recently the adaptation of the Escherichia coli biotin ligase BirA - biotin acceptor sequence (BAS) labeling system to produce human immunodeficiency virus type 1 viruses with biotinylated integrase (NLXIN(B)) and matrix (NLXMA(B)) proteins (Belshan et al., 2009). This report describes the construction of an HIV permissive cell line stably expressing BirA (SupT1.BirA). Consistent with the results in the previous report, NLXMA(B) replicated similar to wild-type levels and expressed biotinylated Gag and MA proteins in the SupT1.BirA cells, whereas the replication of NLXIN(B) was reduced severely. Three additional HIV type 2 (HIV-2) viruses were constructed with the BAS inserted into the vpx and vpr accessory genes. Two BAS insertions were made into the C-terminal half of the Vpx, including one internal insertion, and one at the N-terminus of Vpr. All three viruses were replication competent in the SupT1.BirA cells and their target proteins biotinylated efficiently and incorporated into virions. These results demonstrate the potential utility of the biotinylation system to label and capture HIV protein complexes in the context of replicating virus.
先前的工作最近证明,大肠杆菌生物素连接酶 BirA - 生物素受体序列(BAS)标记系统可以适用于生产带有生物素化整合酶(NLXIN(B))和基质(NLXMA(B))蛋白的人类免疫缺陷病毒 1 型病毒(Belshan 等人,2009 年)。本报告描述了构建稳定表达 BirA(SupT1.BirA)的 HIV 许可细胞系。与之前报告中的结果一致,NLXMA(B)的复制水平与野生型相似,并在 SupT1.BirA 细胞中表达生物素化的 Gag 和 MA 蛋白,而 NLXIN(B)的复制则严重减少。还构建了另外三个带有 BAS 插入到 vpx 和 vpr 辅助基因中的 HIV-2 病毒。在 Vpx 的 C 端半部分中进行了两个 BAS 插入,包括一个内部插入和一个在 Vpr 的 N 端。所有三种病毒在 SupT1.BirA 细胞中均具有复制能力,其靶蛋白能够有效地进行生物素化并掺入病毒粒子中。这些结果表明,生物素化系统在复制病毒的情况下标记和捕获 HIV 蛋白复合物具有潜在的用途。