Department of Medicine, University of Massachusetts Medical School, Worcester, MA 01655, USA.
J Virol Methods. 2011 Jan;171(1):183-9. doi: 10.1016/j.jviromet.2010.10.022. Epub 2010 Oct 27.
A novel HIV-1 Env expression vector (SF162-Z) was developed by introducing two new cloning sites on the backbone of an existing vector that produces a full length Env from HIV-1 SF162 isolate. These sites facilitate the swapping of the gp120 portion of the SF162 Env with matching gp120 antigens from HIV-1 isolates of different genetic clades. Final production of functional pseudotyped viruses will express chimeric Env antigens, including gp41 of the parental SF162 and gp120 from other primary isolates. This system is useful for testing the neutralizing sensitivity of partial env gene products frequently identified in viral quasi species in patients infected with HIV or when only partial gp120 gene products are available.
一种新型的 HIV-1 包膜表达载体(SF162-Z)是通过在现有载体的骨架上引入两个新的克隆位点而开发的,该载体能够从 HIV-1 SF162 分离株中产生全长包膜。这些位点有助于将 SF162 包膜的 gp120 部分与来自不同遗传谱系的 HIV-1 分离株的匹配 gp120 抗原进行交换。最终产生的功能性假型病毒将表达嵌合包膜抗原,包括亲本 SF162 的 gp41 和来自其他原始分离株的 gp120。该系统可用于测试感染 HIV 的患者中病毒准种中经常发现的部分 env 基因产物的中和敏感性,或者当仅存在部分 gp120 基因产物时。