School of Biochemistry & Immunology, Trinity Biomedical Sciences Institute, Trinity College Dublin, Pearse Street, Dublin 2, Ireland.
J Struct Biol. 2013 Jan;181(1):1-10. doi: 10.1016/j.jsb.2012.10.015. Epub 2012 Nov 5.
Poxviruses have evolved numerous mechanisms to evade host innate immunity. Sensory pathways that are activated by Toll-like and nucleotide receptors, as well as innate cell death pathways, are both targets of antagonism by viral proteins. Recent structural, biochemical and functional studies of poxvirus proteins have identified a family of α-helical proteins that adopt a Bcl-2 fold despite highly divergent polypeptide sequences from cellular proteins that regulate apoptosis. These newly identified proteins have assumed new roles in antagonism of NF-κB and interferon signaling pathways and interfere with the release of pro-inflammatory cytokines. Structures of isolated viral proteins and their complexes with cellular targets provide insight into the diverse ways that the Bcl-2 scaffold can be exploited for antagonism of host immunity.
痘病毒进化出了许多机制来逃避宿主先天免疫。Toll 样受体和核苷酸受体激活的感应途径,以及先天细胞死亡途径,都是病毒蛋白拮抗作用的靶点。最近对痘病毒蛋白的结构、生化和功能研究,确定了一组α-螺旋蛋白,它们采用 Bcl-2 折叠,尽管与调节细胞凋亡的细胞蛋白的多肽序列高度不同。这些新鉴定的蛋白在拮抗 NF-κB 和干扰素信号通路方面发挥了新的作用,并干扰了促炎细胞因子的释放。分离的病毒蛋白及其与细胞靶标的复合物的结构,为 Bcl-2 支架被用于拮抗宿主免疫的多种方式提供了深入的了解。