Structure of human complement C8, a precursor to membrane attack

J Mol Biol. 2011 Jan 14;405(2):325-30. doi: 10.1016/j.jmb.2010.10.031. Epub 2010 Nov 10.

Abstract

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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Membrane / metabolism*
  • Complement C8 / chemistry*
  • Complement C8 / metabolism*
  • Complement Membrane Attack Complex / chemistry*
  • Complement Membrane Attack Complex / metabolism*
  • Humans
  • Immunologic Factors / chemistry
  • Immunologic Factors / metabolism
  • Perforin / chemistry
  • Perforin / metabolism*
  • Protein Binding
  • Protein Structure, Tertiary

Substances

  • Complement C8
  • Complement Membrane Attack Complex
  • Immunologic Factors
  • Perforin