Intramolecular general acid catalysis in the binding reactions of α2 and complement components C3 and C4. Issue 6 (June 1981)

• Record Type: Journal Article
• Authors: Davies, Stephen G.; Sim, Robert B.
• Is Part Of: Bioscience reports. Volume 1:Issue 6(1981)
• Page Start: 461
• Page End: 468
• Publication Date: 1981-06
• Subjects: Molecular biology -- Periodicals; Cytology -- Periodicals; 572.8
• DOI: 10.1007/BF01121579
• Languages: English
• ISSNs: 0144-8463

Abstract

Abstract : The complement system proteins C3 and C4 and the plasma protease inhibitor α2 -macroglobulin~ when activated by limited proteolysis, can bind covalently to other macromolecules. The three proteins also exhibit an unusual internal peptide-bond cleavage reaction when denatured. The covalent binding reaction is likely to occur by a transacylation mechanism involving an internal thioiester in the three proteins. However, the activated species of these proteins are much more reactive than simple thiolesters. Studies of molecular models of the thiolester region in C3 show that an intramolecular acid catalysis mechanism can both account for the exceptional reactivity of the activated form of these proteins and provide an explanation for the denaturation-induced peptide bond cleavage.