Biophysics Unit, University of the Basque Country and Spanish Science Research Council (CSIC), PO Box 644, 48080 Bilbao, Spain.
Nat Rev Microbiol. 2012 Jul 2;10(8):563-74. doi: 10.1038/nrmicro2820.
Viroporins are small, hydrophobic proteins that are encoded by a wide range of clinically relevant animal viruses. When these proteins oligomerize in host cell membranes, they form hydrophilic pores that disrupt a number of physiological properties of the cell. Viroporins are crucial for viral pathogenicity owing to their involvement in several diverse steps of the viral life cycle. Thus, these viral proteins, which include influenza A virus matrix protein 2 (M2), HIV-1 viral protein U (Vpu) and hepatitis C virus p7, represent ideal targets for therapeutic intervention, and several compounds that block their pore-forming activity have been identified. Here, we review recent studies in the field that have advanced our knowledge of the structure and function of this expanding family of viral proteins.
病毒离子通道蛋白是由多种临床相关动物病毒编码的小的疏水性蛋白。当这些蛋白质在宿主细胞膜上寡聚化时,它们会形成亲水孔,破坏细胞的许多生理特性。病毒离子通道蛋白在病毒致病性方面非常重要,因为它们参与了病毒生命周期的几个不同步骤。因此,这些病毒蛋白,包括流感 A 病毒基质蛋白 2(M2)、HIV-1 病毒蛋白 U(Vpu)和丙型肝炎病毒 p7,是治疗干预的理想靶点,已经鉴定出几种能够阻断其孔形成活性的化合物。在这里,我们综述了该领域的最新研究进展,这些研究增进了我们对这一家族不断扩大的病毒蛋白的结构和功能的认识。