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

被引:299
作者
Shinzawa-Itoh, Kyoko
Aoyama, Hiroshi
Muramoto, Kazumasa
Terada, Hirohito
Kurauchi, Tsuyoshi
Tadehara, Yoshiki
Yamasaki, Akiko
Sugimura, Takashi
Kurono, Sadamu
Tsujimoto, Kazuo
Mizushima, Tsunehiro
Yamashita, Eiki
Tsukihara, Tomitake
Yoshikawa, Shinya [1 ]
机构
[1] Univ Hyogo, Dept Life Sci, Kamigohri Akoh, Hyogo 6781297, Japan
[2] RIKEN, Harima Inst, Mikazuki Sayo, Hyogo, Japan
[3] Hyogo Med Univ, Dept Mat Sci, Kamigori, Hyogo, Japan
[4] Japan Adv Inst Sci & Technol, Grad Sch Mat Sci, Nomi, Ishikawa, Japan
[5] Osaka Univ, Inst Prot Res, Suita, Osaka 565, Japan
关键词
cytochrome c oxidase; fatty acid structure; mass spectrometry; phospholipids; X-ray structural analysis;
D O I
10.1038/sj.emboj.7601618
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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-D9-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.
引用
收藏
页码:1713 / 1725
页数:13
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