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
The membrane attack complex (MAC) is a hetero-oligomeric protein assembly that kills pathogens by pe...
The complement system is an important part of the mammalian immune defense in blood and interstitial...
In response to complement activation, the membrane attack complex (MAC) assembles from fluid-phase p...
Membrane attack by complement involves the self-assembly on membranes of five hydrophilic proteins (...
The membrane attack complex (MAC) of complement and its precursors, i.e. C5b-7 and C5b-8, were exami...
Polymerization of C9 occurs spontaneously or can be induced by the tetramolecular complex C5b-8. Spo...
Cell injury by complement occurs as a consequence of activation of either the classical or the alter...
The complement system is an important innate immune defense, containing about 30 secreted and membra...
SummaryActivation of the complement system results in formation of membrane attack complexes (MACs),...
Activation of the complement system results in formation of membrane attack complexes (MACs), pores ...
Activation of the complement system results in formation of membrane attack complexes (MACs), pores ...
The membrane-restricted photoactivatable carbene generator 3-(trifluoromethyl)-3-(m-[125I]-iodopheny...
Activation of the complement system results in formation of membrane attack complexes (MACs), pores ...
The human complement system is part of our innate immunity that acts to eliminate pathogenic organis...
Complement component 9 (C9) functions as the pore-forming component of the Membrane Attack Complex (...
The membrane attack complex (MAC) is a hetero-oligomeric protein assembly that kills pathogens by pe...
The complement system is an important part of the mammalian immune defense in blood and interstitial...
In response to complement activation, the membrane attack complex (MAC) assembles from fluid-phase p...
Membrane attack by complement involves the self-assembly on membranes of five hydrophilic proteins (...
The membrane attack complex (MAC) of complement and its precursors, i.e. C5b-7 and C5b-8, were exami...
Polymerization of C9 occurs spontaneously or can be induced by the tetramolecular complex C5b-8. Spo...
Cell injury by complement occurs as a consequence of activation of either the classical or the alter...
The complement system is an important innate immune defense, containing about 30 secreted and membra...
SummaryActivation of the complement system results in formation of membrane attack complexes (MACs),...
Activation of the complement system results in formation of membrane attack complexes (MACs), pores ...
Activation of the complement system results in formation of membrane attack complexes (MACs), pores ...
The membrane-restricted photoactivatable carbene generator 3-(trifluoromethyl)-3-(m-[125I]-iodopheny...
Activation of the complement system results in formation of membrane attack complexes (MACs), pores ...
The human complement system is part of our innate immunity that acts to eliminate pathogenic organis...
Complement component 9 (C9) functions as the pore-forming component of the Membrane Attack Complex (...
The membrane attack complex (MAC) is a hetero-oligomeric protein assembly that kills pathogens by pe...
The complement system is an important part of the mammalian immune defense in blood and interstitial...
In response to complement activation, the membrane attack complex (MAC) assembles from fluid-phase p...