Mapping of functional domains in p47(phox) involved in the activation of NADPH oxidase by 'peptide walking'
| Autor: | Gili Joseph, Edgar Pick, Yara Gorzalczany, Ofra Lotan, Igor Morozov |
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| Rok vydání: | 1998 |
| Předmět: |
Stereochemistry
Protein Conformation Molecular Sequence Data Peptide Spodoptera Biochemistry Peptide Mapping law.invention Cell Line Structure-Activity Relationship law Animals Small GTPase Amino Acid Sequence Molecular Biology Peptide sequence chemistry.chemical_classification Oxidase test NADPH oxidase Binding Sites biology Cell-Free System Dose-Response Relationship Drug NADPH Oxidases Cell Biology Phosphoproteins Peptide Fragments Recombinant Proteins Enzyme Activation chemistry Biotinylation biology.protein Recombinant DNA Proto-oncogene tyrosine-protein kinase Src |
| Zdroj: | The Journal of biological chemistry. 273(25) |
| ISSN: | 0021-9258 |
| Popis: | The superoxide generating NADPH oxidase of phagocytes consists, in resting cells, of a membrane-associated electron transporting flavocytochrome (cytochrome b559) and four cytosolic proteins as follows: p47(phox), p67(phox), p40(phox), and the small GTPase, Rac(1 or 2). Activation of the oxidase is consequent to the assembly of a membrane-localized multimolecular complex consisting of cytochrome b559 and the cytosolic components. We used "peptide walking" (Joseph, G., and Pick, E. (1995) J. Biol. Chem. 270, 29079-29082) for mapping domains in the amino acid sequence of p47(phox) participating in the molecular events leading to the activation of NADPH oxidase. Ninety-five overlapping pentadecapeptides, with a four-residue offset between neighboring peptides, spanning the complete p47(phox) sequence, were tested for the ability to inhibit NADPH oxidase activation in a cell-free system. This consisted of solubilized macrophage membranes, recombinant p47(phox), p67(phox), and Rac1, and lithium dodecyl sulfate, as the activator. Eight functional domains were identified and labeled a-h. These were (N- and C-terminal residue numbers are given for each domain) as follows: a (21-35); b (105-119); c (149-159); d (193-207); e (253-267); f (305-319); g (325-339), and h (373-387). Four of these domains (c, d, e, and g) correspond to or form parts of regions shown before to participate in NADPH oxidase assembly. Thus, domain c corresponds to a region on the N-terminal boundary of the first src homology 3 (SH3) domain, whereas domains d and e represent more precisely defined sites within the full-length first and second SH3 domains, respectively. Domain g overlaps an extensively investigated arginine-rich region. Domains a and b, in the N-terminal half of p47(phox), and domains f and h, in the C-terminal half, represent newly identified entities, for which there is no earlier experimental evidence of involvement in NADPH oxidase activation. "Peptide walking" was also applied to the identification of domains in p47(phox) mediating binding to p67(phox). This was done by quantifying, by enzyme-linked immunosorbent assay, the binding of p67(phox), in solution, to a series of 95 overlapping biotinylated p47(phox) peptides, attached to streptavidin-coated 96-well plates. A single proline-rich domain (residues 357-371) was found to bind p67(phox) in the absence and presence of lithium dodecyl sulfate. |
| Databáze: | OpenAIRE |
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