Hogle James M
Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, Massachusetts 02115, USA.
Annu Rev Microbiol. 2002;56:677-702. doi: 10.1146/annurev.micro.56.012302.160757. Epub 2002 Jan 30.
Structural studies of polio- and closely related viruses have provided a series of snapshots along their cell entry pathways. Based on the structures and related kinetic, biochemical, and genetic studies, we have proposed a model for the cell entry pathway for polio- and closely related viruses. In this model a maturation cleavage of a capsid protein precursor locks the virus in a metastable state, and the receptor acts like a transition-state catalyst to overcome an energy barrier and release the mature virion from the metastable state. This initiates a series of conformational changes that allow the virus to attach to membranes, form a pore, and finally release its RNA genome into the cytoplasm. This model has striking parallels with emerging models for the maturation and cell entry of more complex enveloped viruses such as influenza virus and HIV.
对脊髓灰质炎病毒及密切相关病毒的结构研究,提供了它们进入细胞途径中的一系列瞬间图像。基于这些结构以及相关的动力学、生物化学和遗传学研究,我们提出了脊髓灰质炎病毒及密切相关病毒进入细胞途径的模型。在该模型中,衣壳蛋白前体的成熟切割将病毒锁定在亚稳态,而受体的作用就像过渡态催化剂,以克服能量障碍并将成熟病毒粒子从亚稳态释放出来。这引发了一系列构象变化,使病毒能够附着于细胞膜、形成孔道,并最终将其RNA基因组释放到细胞质中。该模型与流感病毒和HIV等更复杂包膜病毒的成熟及进入细胞的新兴模型有着显著的相似之处。