Direct Interaction of the Novel Nox Proteins with p22phox Is Required for the Formation of a Functionally Active NADPH Oxidase
Open accessAbstract
Nox1 and Nox4, homologues of the leukocyte NADPH oxidase subunit Nox2 (gp91phox) mediate superoxide anion formation in various cell types. However, their interactions with other components of the NADPH oxidase are poorly defined. We determined whether a direct interaction of Nox1 and Nox4 with the p22phox subunit of the NADPH oxidase occurs. Using confocal microscopy, co-localization of p22phox with Nox1, Nox2, and Nox4 was observed in transiently transfected vascular smooth muscle cells (VSMC) and HEK293 cells. Plasmids coding for fluorescent fusion proteins of p22phox and the Nox proteins with cyan- and yellow-fluorescent protein (cfp and yfp, respectively) were constructed and expressed in VSMC and HEK293 cells. The cfp-tagged p22phox expression level increased upon cotransfection with Nox1 or Nox4. Protein-protein interaction between the fluorescent fusion proteins of p22phox and the Nox partners was observed using the fluorescence resonance energy transfer technique. Immunoprecipitation of native Nox1 from human VSMC revealed co-precipitation of p22phox. Immunoprecipitation from transfected HEK293 cells revealed co-precipitation of native p22phox with yfp-tagged Nox1, Nox2, and Nox4. Following mutation of a histidine (corresponding to the position 115 in human Nox2) to leucine, this interaction was abolished. Transfection of rat p22phox (but not Noxo1 and Noxa1) increased the radical generation in cells expressing Nox4. We provide evidence that p22phox directly interacts with Nox1 and Nox4, to form an superoxide-generating NADPH oxidase and demonstrate that mutation of the potential heme binding site in the Nox proteins disrupts the complex formation of Nox1 and Nox4 with p22phox.
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Like Nox2, Nox1 is a transmembrane protein that forms a heterodimer with p22phox and generates O2−.
“Like Nox2, Nox1 is a transmembrane protein which forms a heterodimer with p22 phox and generates O 2 ⅐Ϫ (Ambasta et al., 2004;Kawahara et al., 2005).”
From Neurotoxic Activation of Microglia Is Promoted by a Nox1-Dependent NADPH Oxidase (2008) · cites this paper as Ambasta et al., 2004
The opening summary (p. 1) says Nox1 mediates superoxide formation and directly interacts with p22phox; the Discussion (p. 5) reports their co-precipitation. The Discussion (p. 6) describes membrane localization, but our copy does not establish the more specific claim that Nox1 is transmembrane. (LLM, conf=0.82)
Experimental — accuracy not yet measuredNOX1-4 are associated with another membrane component, p22phox.
“NOX1–4 are associated to another membrane component, p22phox (24).”
From Sources of Vascular Nitric Oxide and Reactive Oxygen Species and Their Regulation (2019) · cites this paper as [24]
NOX1 activation requires p22phox, NOX-organizer 1 (NOXO1), NOX-activator 1 (NOXA1), and the GTPase Rac1.
“NOX1 activation requires p22phox, NOX-organizer 1 (NOXO1), NOX-activator 1 (NOXA1), and the GTPase Rac1 (24, 108, 348).”
From Sources of Vascular Nitric Oxide and Reactive Oxygen Species and Their Regulation (2019) · cites this paper as [24]
NOX4 appears to be constitutively active in the presence of p22phox without the participation of cytosolic proteins.
“NOX4 appears to be constitutively active in the presence of p22phox without the participation of cytosolic proteins (24, 627).”
From Sources of Vascular Nitric Oxide and Reactive Oxygen Species and Their Regulation (2019) · cites this paper as [24]
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References 36 · Cited by 541
Research works printed but not linked: 4
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- Authors
- Ambasta, R. K., Kumar, P., Griendling, K. K., Schmidt, H. H. H. W., Busse, R., & Brandes, R. P.
- Affiliations
- Goethe University Frankfurt (DE)
- Emory University (US)
- Justus-Liebig-Universität Gießen (DE)
- Corresponding author
- Brandes, Ralf P.
- Venue
- Journal of Biological Chemistry
- Publisher
- Elsevier BV
- Published
- 2004-10
- Volume
- 279
- Issue
- 44
- Pages
- 45935-45941
- ISSN
- 0021-9258 (ISSN-L)
- OpenAlex
- W2064358616
- Cited by
- 541
- References
- 36
- Citations by year
- 2026: 7 · 2025: 7 · 2024: 9 · 2023: 13 · 2022: 11 · 2021: 9 · 2020: 20 · 2019: 16 · 2018: 13 · 2017: 26 · 2016: 32 · 2015: 29 · 2014: 24 · 2013: 47 · 2012: 36
- FWCI
- 12.17
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Biological Chemistry (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Publication Server of Goethe University Frankfurt am Main (Goethe University Frankfurt) (submittedVersion, cc-by)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Neutrophil, Myeloperoxidase and Oxidative Mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Redox biology and oxidative stress
- Health Sciences › Medicine › Physiology › Nitric Oxide and Endothelin Effects
- Keywords
- NADPH oxidase, p22phox, NOX1, NOX4, NOX2, gp91phox, protein-protein interaction, superoxide production, heme binding site, vascular smooth muscle cells
- MeSH terms
- NADPH Oxidase 1, NADPH Oxidase 4, Binding Sites, Heme, Humans, Muscle, Smooth, Vascular, NADPH Dehydrogenase, Phosphoproteins, Recombinant Fusion Proteins, NADPH Oxidases, Membrane Transport Proteins, Fluorescence Resonance Energy Transfer
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