ND3 Cys39 in complex I is exposed during mitochondrial respiration. Issue 4 (21st April 2022)
- Record Type:
- Journal Article
- Title:
- ND3 Cys39 in complex I is exposed during mitochondrial respiration. Issue 4 (21st April 2022)
- Main Title:
- ND3 Cys39 in complex I is exposed during mitochondrial respiration
- Authors:
- Burger, Nils
James, Andrew M.
Mulvey, John F.
Hoogewijs, Kurt
Ding, Shujing
Fearnley, Ian M.
Loureiro-López, Marta
Norman, Abigail A.I.
Arndt, Sabine
Mottahedin, Amin
Sauchanka, Olga
Hartley, Richard C.
Krieg, Thomas
Murphy, Michael P. - Abstract:
- Summary: Mammalian complex I can adopt catalytically active (A-) or deactive (D-) states. A defining feature of the reversible transition between these two defined states is thought to be exposure of the ND3 subunit Cys39 residue in the D-state and its occlusion in the A-state. As the catalytic A/D transition is important in health and disease, we set out to quantify it by measuring Cys39 exposure using isotopic labeling and mass spectrometry, in parallel with complex I NADH/CoQ oxidoreductase activity. To our surprise, we found significant Cys39 exposure during NADH/CoQ oxidoreductase activity. Furthermore, this activity was unaffected if Cys39 alkylation occurred during complex I-linked respiration. In contrast, alkylation of catalytically inactive complex I irreversibly blocked the reactivation of NADH/CoQ oxidoreductase activity by NADH. Thus, Cys39 of ND3 is exposed in complex I during mitochondrial respiration, with significant implications for our understanding of the A/D transition and the mechanism of complex I. Graphical abstract: Highlights: ND3-Cys39 in complex I is exposed during active mitochondrial respiration Modification of exposed Cys39 in active complex I does not impair respiration Modification of exposed Cys39 in deactive complex I prevents reactivation Complex I activity and Cys39 exposure are not linked directly Abstract : The enigmatic active/deactive transition of complex I is linked to the exposure state of the critical ND3-Cys39 residue,Summary: Mammalian complex I can adopt catalytically active (A-) or deactive (D-) states. A defining feature of the reversible transition between these two defined states is thought to be exposure of the ND3 subunit Cys39 residue in the D-state and its occlusion in the A-state. As the catalytic A/D transition is important in health and disease, we set out to quantify it by measuring Cys39 exposure using isotopic labeling and mass spectrometry, in parallel with complex I NADH/CoQ oxidoreductase activity. To our surprise, we found significant Cys39 exposure during NADH/CoQ oxidoreductase activity. Furthermore, this activity was unaffected if Cys39 alkylation occurred during complex I-linked respiration. In contrast, alkylation of catalytically inactive complex I irreversibly blocked the reactivation of NADH/CoQ oxidoreductase activity by NADH. Thus, Cys39 of ND3 is exposed in complex I during mitochondrial respiration, with significant implications for our understanding of the A/D transition and the mechanism of complex I. Graphical abstract: Highlights: ND3-Cys39 in complex I is exposed during active mitochondrial respiration Modification of exposed Cys39 in active complex I does not impair respiration Modification of exposed Cys39 in deactive complex I prevents reactivation Complex I activity and Cys39 exposure are not linked directly Abstract : The enigmatic active/deactive transition of complex I is linked to the exposure state of the critical ND3-Cys39 residue, functioning as critical indicator. Burger et al. show that Cys39 is exposed during complex I-linked respiration with important implications for the understanding of the active/deactive transition and complex I function. … (more)
- Is Part Of:
- Cell chemical biology. Volume 29:Issue 4(2022)
- Journal:
- Cell chemical biology
- Issue:
- Volume 29:Issue 4(2022)
- Issue Display:
- Volume 29, Issue 4 (2022)
- Year:
- 2022
- Volume:
- 29
- Issue:
- 4
- Issue Sort Value:
- 2022-0029-0004-0000
- Page Start:
- 636
- Page End:
- 649.e14
- Publication Date:
- 2022-04-21
- Subjects:
- complex I -- active/deactive transition -- Cys39 -- ischemia-reperfusion (IR) injury -- NADH:ubiquinone oxidoreductase -- redox regulation -- mitochondria -- reverse electron transport (RET)
Biochemistry -- Periodicals
572.05 - Journal URLs:
- http://www.cell.com/cell-chemical-biology/home ↗
http://www.sciencedirect.com/ ↗ - DOI:
- 10.1016/j.chembiol.2021.10.010 ↗
- Languages:
- English
- ISSNs:
- 2451-9456
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3097.733000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 21320.xml