The Feinberg School of Medicine, Northwestern University, Chicago, Illinois, USA.
J Virol. 2012 Jun;86(12):6386-93. doi: 10.1128/JVI.00104-12. Epub 2012 Apr 4.
Herpesvirus entry into cells requires coordinated interactions among several viral glycoproteins. The final membrane fusion step of entry is executed by glycoprotein B (gB), a class III viral fusion protein that is conserved across all herpesviruses. Fusion proteins are metastable proteins that mediate fusion by inserting into a target membrane and refolding from a prefusion to postfusion conformation to bring the viral and cell membranes together. Although the structure of gB has been solved in a conformation that likely represents its postfusion form, its prefusion structure and the details of how it refolds to execute fusion are unknown. The postfusion gB structure contains a trimeric coiled-coil at its core and a long C-terminal arm within the ectodomain packs against this coil in an antiparallel manner. This coil-arm complex is reminiscent of the six-helix bundle that provides the energy for fusion in class I fusogens. To determine the role of the coil-arm complex, we individually mutated residues in the herpes simplex virus 1 gB coil-arm complex to alanine and assessed the contribution of each residue to cell-cell and virus-cell fusion. Several coil mutations resulted in a loss of cell surface expression, indicating that the coil residues are important for proper processing of gB. Three mutations in the arm region (I671A, H681A, and F683A) reduced fusion without affecting expression. Combining these three arm mutations drastically reduced the ability of gB to execute fusion; however, fusion function could be restored by adding known hyperfusogenic mutations to the arm mutant. We propose that the formation of the coil-arm complex drives the gB transition to a postfusion conformation and the coil-arm complex performs a function similar to that of the six-helix bundle in class I fusion. Furthermore, we suggest that these specific mutations in the arm may energetically favor the prefusion state of gB.
疱疹病毒进入细胞需要几种病毒糖蛋白之间的协调相互作用。进入的最后一个膜融合步骤由糖蛋白 B(gB)执行,gB 是一种跨所有疱疹病毒保守的 III 类病毒融合蛋白。融合蛋白是一种亚稳蛋白,通过插入靶膜并从预融合构象到融合后构象重折叠来介导融合,从而将病毒和细胞膜融合在一起。尽管 gB 的结构已经在可能代表其融合后构象的构象中得到解决,但它的融合前构象和重折叠以执行融合的细节尚不清楚。融合后的 gB 结构在其核心包含一个三聚体卷曲螺旋,并且在其外域中的长 C 端臂以反平行方式与该螺旋结合。该螺旋-臂复合物使人联想到提供 I 类融合物融合能量的六螺旋束。为了确定螺旋-臂复合物的作用,我们分别将单纯疱疹病毒 1 gB 螺旋-臂复合物中的残基突变为丙氨酸,并评估每个残基对细胞-细胞和病毒-细胞融合的贡献。几个螺旋突变导致细胞表面表达丧失,表明螺旋残基对于 gB 的正确加工很重要。臂区的三个突变(I671A、H681A 和 F683A)降低了融合而不影响表达。将这三个臂突变组合起来大大降低了 gB 执行融合的能力;然而,通过向臂突变体添加已知的超融合突变,可以恢复融合功能。我们提出,螺旋-臂复合物的形成驱动 gB 向融合后构象的转变,并且螺旋-臂复合物执行类似于 I 类融合中的六螺旋束的功能。此外,我们认为臂中的这些特定突变可能在能量上有利于 gB 的融合前状态。