Mia40 imports Cys-containing proteins into the mitochondrial intermembrane space (IMS) by ensuring their Cys-dependent oxidative folding. In this study, we show that the specific Cys of the substrate involved in docking with Mia40 is substrate dependent, the process being guided by an IMS-targeting signal (ITS) present in Mia40 substrates. The ITS is a 9-aa internal peptide that (a) is upstream or downstream of the docking Cys, (b) is sufficient for crossing the outer membrane and for targeting nonmitochondrial proteins, (c) forms an amphipathic helix with crucial hydrophobic residues on the side of the docking Cys and dispensable charged residues on the other side, and (d) fits complementary to the substrate cleft of Mia40 via hydrophobic interactions of micromolar affinity. We rationalize the dual function of Mia40 as a receptor and an oxidase in a two step-specific mechanism: an ITS-guided sliding step orients the substrate noncovalently, followed by docking of the substrate Cys now juxtaposed to pair with the Mia40 active Cys. © 2009 Sideris et al.

A novel intermembrane space-targeting signal docks cysteines onto Mia40 during mitochondrial oxidative folding / D.P.Sideris; N.Petrakis; N.Katrakili; D.Mikropoulou; A.Gallo; S.Ciofi Baffoni; L.Banci; I.Bertini; K.Tokatlidis. - In: THE JOURNAL OF CELL BIOLOGY. - ISSN 0021-9525. - STAMPA. - 187:(2009), pp. 1007-1022. [10.1083/jcb.200905134]

A novel intermembrane space-targeting signal docks cysteines onto Mia40 during mitochondrial oxidative folding

GALLO, ANGELO;CIOFI BAFFONI, SIMONE;BANCI, LUCIA;BERTINI, IVANO;
2009

Abstract

Mia40 imports Cys-containing proteins into the mitochondrial intermembrane space (IMS) by ensuring their Cys-dependent oxidative folding. In this study, we show that the specific Cys of the substrate involved in docking with Mia40 is substrate dependent, the process being guided by an IMS-targeting signal (ITS) present in Mia40 substrates. The ITS is a 9-aa internal peptide that (a) is upstream or downstream of the docking Cys, (b) is sufficient for crossing the outer membrane and for targeting nonmitochondrial proteins, (c) forms an amphipathic helix with crucial hydrophobic residues on the side of the docking Cys and dispensable charged residues on the other side, and (d) fits complementary to the substrate cleft of Mia40 via hydrophobic interactions of micromolar affinity. We rationalize the dual function of Mia40 as a receptor and an oxidase in a two step-specific mechanism: an ITS-guided sliding step orients the substrate noncovalently, followed by docking of the substrate Cys now juxtaposed to pair with the Mia40 active Cys. © 2009 Sideris et al.
2009
187
1007
1022
D.P.Sideris; N.Petrakis; N.Katrakili; D.Mikropoulou; A.Gallo; S.Ciofi Baffoni; L.Banci; I.Bertini; K.Tokatlidis
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Utilizza questo identificatore per citare o creare un link a questa risorsa: https://hdl.handle.net/2158/368793
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