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Structure of human complement C8, a precursor to membrane attack.

Journal of molecular biology (2010-11-16)
Doryen Bubeck, Pietro Roversi, Rossen Donev, B Paul Morgan, Oscar Llorca, Susan M Lea
ZUSAMMENFASSUNG

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.

MATERIALIEN
Produktnummer
Marke
Produktbeschreibung

Sigma-Aldrich
Complement C8 from human serum, suitable for radioiodination, RIA, ≥85% (SDS-PAGE), ≥125,000 C8H50 units/mg protein (using C8 deficient serum)
Sigma-Aldrich
Anti-C8B (AB2) antibody produced in rabbit, affinity isolated antibody