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

• DOI: 10.1038/sj.emboj.7601618
• Publication Date: 2007-03-02T01:46:21Z
• Authors: Kyoko Shinzawa-Itoh; Hiroshi Aoyama; Kazumasa Muramoto; Hirohito Terada; Tsuyoshi Kurauchi; Yoshiki Tadehara; Akiko Yamasaki; Takashi Sugimura; Sadamu Kurono; Kazuo Tsujimoto; Tsunehiro Mizushima; Eiki Yamashita; Tomitake Tsukihara; Shinya Yoshikawa
• Keywords: Models, Molecular; 0301 basic medicine; Binding Sites; Chromatography, Gas; Molecular Structure; Myocardium; Oleic Acids; Lipids; Electron Transport Complex IV; Evolution, Molecular; 03 medical and health sciences; Absorptiometry, Photon; Tandem Mass Spectrometry; Animals; Cattle; Paracoccus denitrificans

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 O(2) transfer pathway of CcO causes two palmitate tails of phosphatidylglycerols to block the pathway, suggesting that the palmitates control the O(2) transfer process.The phosphatidylglycerol with vaccenate (cis-Delta(11)-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-Delta(9)-octadecenoate). The X-ray structure indicates that the protein moiety selects cis-vaccenate near the O(2) transfer pathway against trans-vaccenate. These results suggest that vaccenate plays a critical role in the O(2) transfer mechanism.