The Journal of Biochemistry · 2012 · 11 citations · 26 references
Life SciencesBiochemistryMolecular BiologyEnzymologyProtein BiochemistrySignal TransductionEnzyme FunctionProtein DomainsProtein Interaction DomainsProtein StructureProteolytic EnzymesProteolytic ProcessingCatalytic DomainsLow-density Lipoprotein Receptor FamilyProteolytic Activation MechanismsSerine Protease MechanismTransient ExpressionTransient Expression SystemsZymogen Activation In Coagulation
Matriptase is a type II transmembrane serine protease containing two complement proteases C1r/C1s-urchin embryonic growth factor-bone morphogenetic protein domains (CUB repeat) and four low-density lipoprotein receptor class A domains (LDLRA repeat). The single-chain zymogen of matriptase has been found to exhibit substantial protease activity, possibly causing its own activation (i.e. conversion to a disulfide-linked two-chain fully active form), although the activation seems to be mediated predominantly by two-chain molecules. Our aim was to assess the roles of CUB and LDLRA repeats in zymogen activation. Transient expression studies of soluble truncated constructs of recombinant matriptase in COS-1 cells showed that the CUB repeat had an inhibitory effect on zymogen activation, possibly because it facilitated the interaction of two-chain molecules with a matriptase inhibitor, hepatocyte growth factor activator inhibitor type-1. By contrast, the LDLRA repeat had a promoting effect on zymogen activation. The effect of the LDLRA repeat seems to reflect its ability to increase zymogen activity. The proteolytic activities were higher in pseudozymogen forms of recombinant matriptase containing the LDLRA repeat than in a pseudozymogen without the repeat. Our findings provide new insights into the roles of these non-catalytic domains in the generation of active matriptase.
26
Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4
Ulrich K. Laemmli · Nature · 1970 · 251.6K citations
Peer Bork, Georg Beckmann · Journal of Molecular Biology · 1993 · 580 citations
Toshihiko Takeuchi, Jennifer L. Harris, Wei Huang et al. · Journal of Biological Chemistry · 2000 · 437 citations · Full text
Molecular basis of familial hypercholesterolaemia from structure of LDL receptor module
Deborah Fass, Stephen C. Blacklow, Peter S. Kim et al. · Nature · 1997 · 339 citations