Subunit composition of mitochondrial complex I from the yeast Yarrowia lipolytica

• Published in: Biochimica et biophysica acta 2004-07, Vol.1658 (1), p.148-156
• Main Authors: Abdrakhmanova, Albina, Zickermann, Volker, Bostina, Mihnea, Radermacher, Michael, Schägger, Hermann, Kerscher, Stefan, Brandt, Ulrich
• Format: Article
• Language: English
• Subjects: Accessory subunit; Amino Acid Sequence; Base Sequence; Complex I; Electron Transport Complex I - chemistry; Electron Transport Complex I - metabolism; Electrophoresis, Gel, Two-Dimensional; Mass spectrometry; Mitochondria - enzymology; Mitochondrial Proteins - chemistry; Mitochondrial Proteins - genetics; Molecular Sequence Data; NADH:ubiquinone oxidoreductase; Protein Subunits - analysis; Protein Subunits - genetics; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization; Yarrowia - enzymology; Yarrowia - genetics; Yarrowia lipolytica
• ISSN: 0005-2728; 0006-3002; 1879-2650
• DOI: 10.1016/j.bbabio.2004.04.019

Here we present a first assessment of the subunit inventory of mitochondrial complex I from the obligate aerobic yeast Yarrowia lipolytica. A total of 37 subunits were identified. In addition to the seven central, nuclear coded, and the seven mitochondrially coded subunits, 23 accessory subunits were found based on 2D electrophoretic and mass spectroscopic analysis in combination with sequence information from the Y. lipolytica genome. Nineteen of the 23 accessory subunits are clearly conserved between Y. lipolytica and mammals. The remaining four accessory subunits include NUWM, which has no apparent homologue in any other organism and is predicted to contain a single transmembrane domain bounded by highly charged extramembraneous domains. This structural organization is shared among a group of 7 subunits in the Y. lipolytica and 14 subunits in the mammalian enzyme. Because only five of these subunits display significant evolutionary conservation, their as yet unknown function is proposed to be structure- rather than sequence-specific. The NUWM subunit could be assigned to a hydrophobic subcomplex obtained by fragmentation and sucrose gradient centrifugation. Its position within the membrane arm was determined by electron microscopic single particle analysis of Y. lipolytica complex I decorated with a NUWM-specific monoclonal antibody.