C3-convertase


C3 convertase belongs to family of serine proteases and is necessary in innate immunity as a part of the complement system which eventuate in opsonisation of particles, release of inflammatory peptides, C5 convertase formation and cell lysis.
C3 convertase can be used to refer to the form produced in the alternative pathway or the classical and lectin pathways. Once formed, both C3 convertases will catalyze the proteolytic cleavage of C3 into C3a and C3b.
The smaller fragment called C3a serves to increase vascular permeability and promote extravasation of phagocytes, while the larger C3b fragment can be used as an opsonin or bind to either type of C3 convertase to form the trimolecular C5 convertase to activate C5 for the membrane attack complex.

Formation

C3 convertase formation can occur in three different pathways: the classical, lectin, and alternative pathways.

Alternative pathway

Cleavage of complement C3 by a free floating convertase, thrombin, plasmin or even a bacterial enzyme leads to formation of C3a and C3b fragments. C3b, the larger fragment, becomes covalently attached to the microbial surface or to the antibody molecules through the thioester domain at the site of complement activation. After cleavage and binding to cell surface, the C3b fragment is ready to bind a plasma protein called Factor B. The Factor B is cleaved by a plasma serine protease Factor D releasing a small fragment called Ba and generating a larger fragment called Bb that remains attached to C3b. Also Mg2+ ions are necessary for forming a functional C3 convertase. Thus, the alternative C3 convertase is formed and is able to cleave C3 via its dimeric Bb subunit.
Since C3 convertases cleave C3 to produce C3b which can then form an additional C3 convertase through the alternative pathway, this is a potential mechanism of signal amplification in the complement cascade resulting in the deposition of large numbers of C3b molecules on the surface of activating particles, enabling opsonisation and acute local inflammation.

Classical and lectin pathways

The C3 convertase formed in the classical or lectin pathways is formed of C4b and C2b instead. The cleavage of C4 and C2 is mediated by serine proteases. In the classical pathway, this is by sequential proteolytic activation of proteins within the C1 complex in response to binding to CRP or immunoglobulin, and in the lectin pathway it is driven by mannose binding lectin and its associated serine proteases.
C4 is homologous to C3 in that it contains an internal thioester bond that ends up on C4b. Thus it can form covalent amide or ester linkages with the plasma membrane of the pathogen and any associated antibodies, where it then behaves as an opsonin. The larger C2b produced by C2 hydrolysis attaches to the C4b to form the classical C3 convertase, C4b2b.
The smaller fragments of proteolysis, C4a and C2a are released. C4a is an anaphylatoxin.

Regulation

Nevertheless, this positive feedback mechanism can be regulated by binding of the control protein, nonproteolytic glycoprotein β1H, to C3b, which prevents association of factor B, and facilitates the decay-dissociation of Bb in the C3bBb complex, in addition to enhancing proteolytic inactivation of C3b by C3b inactivator.
Membrane-associated sialic acid promotes high-affinity binding of β1H to C3b without influencing the affinity of B for C3b.
Decay-accelerating factor is another negative regulator of C3 convertase. It is a membrane protein and regulates also C5 convertase of the classical and alternative pathway. DAF protects host cells from damage by autologous complement. DAF acts on C2b and Bb and dissociates them rapidly from C4b and C3b – thereby preventing the assembly of the C3 convertase.
C4 binding protein interferes with the assembly of the membrane-bound C3 convertase of the classical pathway. C4BP is a cofactor for the enzyme C3bINA. C4b-binding protein inhibits the haemolytic function of cell-bound C4b. C4b-binding protein and C3b inactivator control the C3 convertase of the classical pathway in a similar way to that described for β1H and C3b inactivator in the alternative pathway.
C3b has different binding site for C3bINA, β1H, factor B and properdin. Binding β1H to C3b increases C3bINA binding, while factor B binding prevents C3bINA binding and is competitive with β1H binding.
Regulation of the amplification phase of the alternative pathway is exerted by multiple mechanisms:
The genes encoding C2, C4 and factor B are located on chromosome 6 between the B locus of class I products and the D locus of class II products in the MHC.