发布: 2014年05月20日第4卷第10期 DOI: 10.21769/BioProtoc.1134 浏览次数: 8094
评审: Anonymous reviewer(s)
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诱导型HIV-1库削减检测(HIVRRA):用于评估外周血单个核细胞中HIV-1潜伏库清除策略毒性与效力的快速敏感方法
Jade Jansen [...] Neeltje A. Kootstra
2025年07月20日 1219 阅读
Abstract
As for all positive strand RNA viruses, hepatitis C virus (HCV) RNA replication is tightly associated with rearranged host cell membranes, termed viral replication factories. However, up to now little is known about both viral and cellular constituents of viral replication factories. Here, we describe a protocol to specifically isolate HCV-remodeled host cell membranes and endoplasmic reticulum (ER) membranes of naïve cells, by using a functional NS4B HA-tagged subgenomic replicon and a C-terminally HA-tagged calnexin-overexpressing cell line, respectively. Post-nuclear whole cell membrane fractions are first enriched by density gradient centrifugation, followed by HA-specific affinity tag purification. Upon elution under native conditions, purified samples can be subject to a variety of biochemical and functional assays.
Keywords: Hepatitis c virus (丙型肝炎病毒)Materials and Reagents
Equipment
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文章信息
版权信息
© 2014 The Authors; exclusive licensee Bio-protocol LLC.
如何引用
Paul, D. and Bartenschlager, R. (2014). Purification of HCV-remodeled and Control ER Membranes. Bio-protocol 4(10): e1134. DOI: 10.21769/BioProtoc.1134.
分类
微生物学 > 微生物-宿主相互作用 > 病毒
细胞生物学 > 细胞器分离 > 细胞膜
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