Structures and physiological roles of 13 integral lipids of bovine heart cytochrome c oxidase

All 13 lipids, including two cardiolipins, one phosphatidylcholine, three phosphatidylethanolamines, four phosphatidylglycerols and three triglycerides, were identified in a crystalline bovine heart cytochrome c oxidase (CcO) preparation. The chain lengths and unsaturated bond positions of the fatty acid moieties determined by mass spectrometry suggest that each lipid head group identifies its specific binding site within CcOs. The X‐ray structure demonstrates that the flexibility of the fatty acid tails facilitates their effective space‐filling functions and that the four phospholipids stabilize the CcO dimer. Binding of dicyclohexylcarbodiimide to the O2 transfer pathway of CcO causes two palmitate tails of phosphatidylglycerols to block the pathway, suggesting that the palmitates control the O2 transfer process.The phosphatidylglycerol with vaccenate (cis‐Δ11‐octadecenoate) was found in CcOs of bovine and Paracoccus denitrificans, the ancestor of mitochondrion, indicating that the vaccenate is conserved in bovine CcO in spite of the abundance of oleate (cis‐Δ9‐octadecenoate). The X‐ray structure indicates that the protein moiety selects cis‐vaccenate near the O2 transfer pathway against trans‐vaccenate. These results suggest that vaccenate plays a critical role in the O2 transfer mechanism.

[1]  D. Hunneman,et al.  Isolation and characterization of an ornithine-containing lipid from Paracoccus denitrificans. , 1980, European journal of biochemistry.

[2]  C Menzel,et al.  Protein, lipid and water organization in bacteriorhodopsin crystals: a molecular view of the purple membrane at 1.9 A resolution. , 1999, Structure.

[3]  S. Yoshikawa,et al.  Steady-State Kinetics of NADH:coenzyme Q Oxidoreductase Isolated from Bovine Heart Mitochondria , 2002, Journal of bioenergetics and biomembranes.

[4]  S. Iwata,et al.  The X-ray crystal structures of wild-type and EQ(I-286) mutant cytochrome c oxidases from Rhodobacter sphaeroides. , 2002, Journal of molecular biology.

[5]  B. Trumpower,et al.  Specific roles of protein–phospholipid interactions in the yeast cytochrome bc1 complex structure , 2001, The EMBO journal.

[6]  T. Tomizaki,et al.  Structures of metal sites of oxidized bovine heart cytochrome c oxidase at 2.8 A , 1995, Science.

[7]  A. Puustinen,et al.  Channelling of dioxygen into the respiratory enzyme. , 1996, Biochimica et biophysica acta.

[8]  H. Michel,et al.  The Cytochrome c Oxidase from Paracoccus denitrificans Does Not Change the Metal Center Ligation upon Reduction* , 1999, The Journal of Biological Chemistry.

[9]  T. Tomizaki,et al.  The Whole Structure of the 13-Subunit Oxidized Cytochrome c Oxidase at 2.8 Å , 1996, Science.

[10]  A. Cámara-Artigas,et al.  Interactions between lipids and bacterial reaction centers determined by protein crystallography , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[11]  S. Yoshikawa,et al.  The low-spin heme of cytochrome c oxidase as the driving element of the proton-pumping process , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[12]  M. Kates,et al.  A novel glycolipid and phospholipid in the purple membrane. , 2000, Biochemistry.

[13]  S. Weintraub,et al.  Photolabeling of cardiolipin binding subunits within bovine heart cytochrome c oxidase. , 2006, Biochemistry.

[14]  G. Daum,et al.  Lipids of mitochondria. , 1985, Biochimica et biophysica acta.

[15]  J. Walker,et al.  Large-scale chromatographic purification of F1F0-ATPase and complex I from bovine heart mitochondria. , 1996, The Biochemical journal.

[16]  K. Shinzawa-Itoh,et al.  Crystallization and preliminary X-ray crystallographic studies of bovine heart mitochondrial cytochrome bc1 complex. , 1991, Journal of molecular biology.

[17]  P. Brzezinski,et al.  Subunit III of cytochrome c oxidase of Rhodobacter sphaeroides is required to maintain rapid proton uptake through the D pathway at physiologic pH. , 2003, Biochemistry.

[18]  R. Capaldi,et al.  Inhibition of cytochrome c oxidase function by dicyclohexylcarbodiimide. , 1981, Biochimica et biophysica acta.

[19]  M. Thelen,et al.  Dicyclohexylcarbodiimide binds specifically and covalently to cytochrome c oxidase while inhibiting its H+-translocating activity. , 1980, The Journal of biological chemistry.

[20]  M. L. Connolly Solvent-accessible surfaces of proteins and nucleic acids. , 1983, Science.

[21]  M R Jones,et al.  Structural details of an interaction between cardiolipin and an integral membrane protein. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[22]  D. Marsh,et al.  Lipid conformation in crystalline bilayers and in crystals of transmembrane proteins. , 2006, Chemistry and physics of lipids.