Functional Insights from the Structure of the Multifunctional C345C Domain of C5 of Complement
| Autor: | Dinesh C. Soares, Ronald T. Ogata, Paul N. Barlow, Dušan Uhrín, Janice Bramham, Chuong-Thu Thai |
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| Rok vydání: | 2005 |
| Předmět: |
Models
Molecular Protein Folding Magnetic Resonance Spectroscopy Time Factors Lysis Protein Conformation Genetic Vectors Molecular Sequence Data Static Electricity Oligonucleotides Oligosaccharides Complement factor I Biology Biochemistry Protein Structure Secondary law.invention law Escherichia coli Humans Point Mutation Amino Acid Sequence Molecular Biology chemistry.chemical_classification Sequence Homology Amino Acid Oligonucleotide C-terminus Cell Membrane Complement C5 Stereoisomerism Cell Biology Surface Plasmon Resonance Complement C7 Recombinant Proteins Complement C6 Protein Structure Tertiary Complement system Kinetics Enzyme chemistry Biophysics Recombinant DNA Complement membrane attack complex Protein Binding |
| Zdroj: | Journal of Biological Chemistry. 280:10636-10645 |
| ISSN: | 0021-9258 |
| DOI: | 10.1074/jbc.m413126200 |
| Popis: | The complement protein C5 initiates assembly of the membrane attack complex. This remarkable process results in lysis of target cells and is fundamental to mammalian defense against infection. The 150-amino acid residue domain at the C terminus of C5 (C5-C345C) is pivotal to C5 function. It interacts with enzymes that convert C5 to C5b, the first step in the assembly of the membrane attack complex; it also binds to the membrane attack complex components C6 and C7 with high affinity. Here a recombinant version of this C5-C345C domain is shown to adopt the oligosaccharide/oligonucleotide binding fold, with two helices packed against a five-stranded beta-barrel. The structure is compared with those from the netrin-like module family that have a similar fold. Residues critical to the interaction with C5-convertase cluster on a mobile, hydrophobic inter-strand loop that protrudes from the open face of the beta-barrel. The opposite, helix-dominated face of C5-C345C carries a pair of exposed hydrophobic side chains adjacent to a striking negatively charged patch, consistent with affinity for positively charged factor I modules in C6 and C7. Modeling of homologous domains from complement proteins C3 and C4, which do not participate in membrane attack complex assembly, suggests that this provisionally identified C6/C7-interacting face is indeed specific to C5. |
| Databáze: | OpenAIRE |
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