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PMID: 6379417 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S. Review

Membrane attack by complement.

Molecular immunology ·Vol. 21 ·No. 7 ·1984-07-00 ·Pages 589-603

Podack ER, Tschopp J

Abstract

Membrane attack by complement involves the self-assembly on membranes of five hydrophilic proteins (C5b, C6, C7, C8 and C9) to an amphiphilic tubular complex comprising approximately 20 subunits. The hydrophilic-amphiphilic transition of the precursor proteins is achieved by restricted unfolding and exposure of previously hidden hydrophobic domains. Restricted unfolding, in turn, is driven by high-affinity protein-protein interactions resulting in the formation of amphilic complexes. Circular polymerization of C9 to a tubular complex (poly C9) constitutes the molecular mechanism for transmembrane channel assembly and formation of ultrastructural membrane lesions.

MeSH Terms
Animals Biopolymers Cell Membrane/immunology Chemical Phenomena Chemistry Complement Activation Complement C5/metabolism Complement C6/metabolism Complement C7/metabolism Complement C8/metabolism Complement C9/metabolism Complement Membrane Attack Complex Complement System Proteins/metabolism Models, Chemical Protein Conformation
Chemicals
Biopolymers Complement C5 Complement C6 Complement C7 Complement C8 Complement C9 Complement Membrane Attack Complex Complement System Proteins
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Podack E R
Tschopp J
Article Info
Journal
Molecular immunology
Abbr.
Mol Immunol
ISSN
0161-5890
Published
1984-07-00
Pages
589-603
Language
English
Region
England
NLM ID
7905289
Subset
IM
Grants
NIAID NIH HHS · AI 18525 · United States
NCI NIH HHS · CA 34524 · United States
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