Literature DB >> 9177307

Synthetic peptides corresponding to various hydrophilic regions of the large subunit of cytochrome b558 inhibit superoxide generation in a cell-free system from neutrophils.

M Y Park1, S Imajoh-Ohmi, H Nunoi, S Kanegasaki.   

Abstract

Cytochrome b558 is a component of the superoxide-generating system in neutrophils and plays key roles in both the assembly of a functional complex with cytosolic proteins and shuttling an electron from NADPH to molecular oxygen. To determine the role of predicted hydrophilic domains of gp91-phox, a glycosylated subunit of the cytochrome, we synthesized peptides corresponding to the regions and tested whether they affected superoxide generation in the cell-free system obtained from human neutrophils. Among twelve peptides tested, six peptides, four of which correspond to previously unreported regions, inhibited superoxide generation in the cell-free system. All of the active peptides were effective when added to the system before activation with sodium dodecyl sulfate. Four peptides, including two peptides corresponding to two newly identified regions, inhibited the translocation of the cytosolic components, p47-phox and p67-phox. The extent of inhibition on translocation of these components varied depending on the peptide used.

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Year:  1997        PMID: 9177307     DOI: 10.1006/bbrc.1997.6672

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  9 in total

1.  Assembly of the neutrophil respiratory burst oxidase: a direct interaction between p67PHOX and cytochrome b558.

Authors:  P M Dang; A R Cross; B M Babior
Journal:  Proc Natl Acad Sci U S A       Date:  2001-03-13       Impact factor: 11.205

Review 2.  Assembly of the phagocyte NADPH oxidase.

Authors:  William M Nauseef
Journal:  Histochem Cell Biol       Date:  2004-08-04       Impact factor: 4.304

3.  Regulation of NADPH oxidase activity in phagocytes: relationship between FAD/NADPH binding and oxidase complex assembly.

Authors:  Franck Debeurme; Antoine Picciocchi; Marie-Claire Dagher; Didier Grunwald; Sylvain Beaumel; Franck Fieschi; Marie-José Stasia
Journal:  J Biol Chem       Date:  2010-08-19       Impact factor: 5.157

4.  Constitutive NADPH oxidase 4 activity resides in the composition of the B-loop and the penultimate C terminus.

Authors:  Katharina von Löhneysen; Deborah Noack; Patti Hayes; Jeffrey S Friedman; Ulla G Knaus
Journal:  J Biol Chem       Date:  2012-01-25       Impact factor: 5.157

5.  Nox4 B-loop creates an interface between the transmembrane and dehydrogenase domains.

Authors:  Heather M Jackson; Tsukasa Kawahara; Yukio Nisimoto; Susan M E Smith; J David Lambeth
Journal:  J Biol Chem       Date:  2010-02-05       Impact factor: 5.157

Review 6.  Combating oxidative stress in vascular disease: NADPH oxidases as therapeutic targets.

Authors:  Grant R Drummond; Stavros Selemidis; Kathy K Griendling; Christopher G Sobey
Journal:  Nat Rev Drug Discov       Date:  2011-06       Impact factor: 84.694

Review 7.  Towards specific NADPH oxidase inhibition by small synthetic peptides.

Authors:  Jamel El-Benna; Pham My-Chan Dang; Axel Périanin
Journal:  Cell Mol Life Sci       Date:  2012-05-06       Impact factor: 9.261

Review 8.  Strategies for identifying synthetic peptides to act as inhibitors of NADPH oxidases, or "all that you did and did not want to know about Nox inhibitory peptides".

Authors:  Iris Dahan; Edgar Pick
Journal:  Cell Mol Life Sci       Date:  2012-05-06       Impact factor: 9.261

Review 9.  NADPH oxidase inhibitors: a decade of discovery from Nox2ds to HTS.

Authors:  Eugenia Cifuentes-Pagano; Gabor Csanyi; Patrick J Pagano
Journal:  Cell Mol Life Sci       Date:  2012-05-15       Impact factor: 9.261

  9 in total

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