Kielian M, Jungerwirth S
Department of Cell Biology, Albert Einstein College of Medicine, Bronx, NY 10461.
Mol Biol Med. 1990 Feb;7(1):17-31.
Enveloped animal viruses enter their host cells by a process of membrane fusion. This fusion can occur at the cell plasma membrane or within the endocytic vacuolar system, depending on the characteristics of the virus fusion protein. Examples of both pathways of viral entry are detailed in this review. Semliki Forest virus (SFV) is presented as a well-studied prototype of those viruses which use endocytic uptake in order to infect cells. Fusion of endocytosed SFV is specifically triggered by the acidic pH present within the endocytic pathway, which causes specific conformational changes in the SFV spike protein. While the overall features of endocytic uptake are similar for all viruses which use this pathway, the mechanism by which the viruses then cause fusion appears to differ significantly between them. The best understood fusion mechanism is that of influenza virus, for which sequences involved in pH-dependent fusion can be correlated with the crystallographic structure of the spike protein. In contrast to these pH-dependent virus systems, the entry of human immunodeficiency virus (HIV) into cells occurs by a pH-independent fusion mechanism probably involving fusion at the plasma membrane. The data to date on HIV fusion, endocytosis and entry are summarized as an example of this pathway.
有包膜的动物病毒通过膜融合过程进入宿主细胞。这种融合可发生在细胞质膜或内吞泡系统内,这取决于病毒融合蛋白的特性。本综述详细介绍了病毒进入的这两种途径。辛德毕斯病毒(SFV)被作为那些利用内吞摄取来感染细胞的病毒的一个深入研究的原型。内吞的SFV的融合是由内吞途径中存在的酸性pH特异性触发的,这会导致SFV刺突蛋白发生特定的构象变化。虽然所有利用这种途径的病毒的内吞摄取的总体特征相似,但这些病毒随后导致融合的机制在它们之间似乎有很大差异。理解得最清楚的融合机制是流感病毒的融合机制,其与pH依赖性融合有关的序列可以与刺突蛋白的晶体结构相关联。与这些pH依赖性病毒系统不同,人类免疫缺陷病毒(HIV)进入细胞是通过一种可能涉及在质膜融合的pH非依赖性融合机制。作为该途径的一个例子,总结了迄今为止关于HIV融合、内吞作用和进入的数据。