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Cleavage of C4b by C3b inactivator: production of a nicked form of C4b, C4b', as an intermediate cleavage product of C4b by C3b inactivator.

Shigeharu Nagasawa, +2 more
- 01 Aug 1980 - 
- Vol. 125, Iss: 2, pp 578-582
TLDR
In both cleavage reactions, a high m.w. cofactor protein, C4bC3bINACo, which is the same protein described as the C4 binding protein, was required, suggesting that both of the proteolytic processes are catalyzed by the C3bINA.
Abstract
We have investigated the mechanism of cleavage of C4b into C4c and C4d by the C3b inactivator (C3bINA) and revealed the formation of a nicked form of C4b as an intermediate cleavage product. The cleavage of C4b by the C3bINA was a two-step reaction. The first cleavage occurred on the alpha-chain (89,000 daltons) yielding two fragments, 73,000 daltons and 16,000 daltons. These fragments were bound to each other or to the beta or gamma chain through disulfide linkages. Therefore, an altered form of C4b, C4b', consisting of four disulfide-linked polypeptide chains with the same m.w. as C4b, was produced as an intermediate cleavage product. Subsequently, the second cleavage occurred on the alpha-chain fragment of 73,000 daltons to produce the two generally recognized fragments, C4c and C4d. In both cleavage reactions, a high m.w. cofactor protein, C4bC3bINACo, which is the same protein described as the C4 binding protein, was required, suggesting that both of the proteolytic processes are catalyzed by the C3bINA.

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Purification and characterization of a membrane protein (gp45-70) that is a cofactor for cleavage of C3b and C4b.

TL;DR: This protein was the most efficient (50 times that of H) yet-described cofactor for the I-mediated first cleavage of C3b and also was a cofactor of C4b, but was not as efficient as C4bp.
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High molecular weight complex in human plasma between vitamin K-dependent protein S and complement component C4b-binding protein.

TL;DR: There is an equilibrium between free and bound protein S in plasma, a recently described vitamin K-dependent plasma protein, which is shown to exist in two forms in plasma--free protein and in complex with C4b-binding protein.
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Protein S and C4b-binding protein: components involved in the regulation of the protein C anticoagulant system.

TL;DR: Anticoagulation may not be the sole function of protein S, since both in vivo and in vitro, it forms a high affinity non-covalent complex with one of the regulatory proteins in the complement system, the C4b-binding protein (C4BP).
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Membrane complement receptors specific for bound fragments of C3.

TL;DR: In this paper, the membrane receptors for bound fragments of C3l play a pivotal role in complement activation, and C3-derived fragments are both liberated into the fluid phase and covalently bound to the substrate.
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Purification of human C4b-binding protein and formation of its complex with vitamin K-dependent protein S

TL;DR: C4b-binding protein was purified from human plasma in high yield by a simple procedure involving barium citrate adsorption and two subsequent chromatographic steps, indicating two forms differing slightly from each other in molecular weight and net charge.
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