生物
合胞体
融合机制
细胞融合
脂质双层融合
细胞生物学
病毒包膜
病毒进入
跨膜蛋白
病毒
膜蛋白
病毒学
细胞
病毒复制
遗传学
膜
受体
作者
Marta Ciechonska,Roy Duncan
标识
DOI:10.1016/j.tim.2014.08.005
摘要
Reovirus fusion-associated small transmembrane (FAST) proteins are the only known nonenveloped virus fusogens and are dedicated to inducing cell-to-cell, not virus–cell, membrane fusion. Numerous structural and functional attributes distinguish this novel family of viral fusogens from all enveloped virus membrane fusion proteins. Both families of viral fusogens play key roles in virus dissemination and pathogenicity, but employ different mechanisms to mediate membrane apposition and merger. However, convergence of these distinct families of viral membrane fusion proteins on common pathways needed for pore expansion and syncytium formation suggests syncytiogenesis represents a cellular response to the presence of cell–cell fusion pores. Together, FAST proteins and enveloped virus fusion proteins provide exceptional insights into the ubiquitous process of cell–cell membrane fusion and syncytium formation.
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