University of Oxford, Wellcome Trust Centre for Human Genetics, Oxford OX3 7BN, UK.
J Mol Biol. 2011 Jan 14;405(2):325-30. doi: 10.1016/j.jmb.2010.10.031. Epub 2010 Nov 10.
Complement component C8 plays a pivotal role in the formation of the membrane attack complex (MAC), an important antibacterial immune effector. C8 initiates membrane penetration and coordinates MAC pore formation. High-resolution structures of C8 subunits have provided some insight into the function of the C8 heterotrimer; however, there is no structural information describing how the intersubunit organization facilitates MAC assembly. We have determined the structure of C8 by electron microscopy and fitted the C8α-MACPF (membrane attack complex/perforin)-C8γ co-crystal structure and a homology model for C8β-MACPF into the density. Here, we demonstrate that both the C8γ protrusion and the C8α-MACPF region that inserts into the membrane upon activation are accessible.
补体成分 C8 在膜攻击复合物(MAC)的形成中起着关键作用,MAC 是一种重要的抗菌免疫效应因子。C8 启动膜穿透并协调 MAC 孔形成。C8 亚基的高分辨率结构为 C8 三聚体的功能提供了一些见解;然而,没有结构信息描述亚基间的组织如何促进 MAC 的组装。我们通过电子显微镜确定了 C8 的结构,并将 C8α-MACPF(膜攻击复合物/穿孔素)-C8γ 共晶体结构和 C8β-MACPF 的同源模型拟合到密度中。在这里,我们证明了激活时插入膜中的 C8γ 突出部和 C8α-MACPF 区域都是可及的。