A¦Â/Cu-catalyzed oxidation of cholesterol in 1,2-dipalmitoyl phosphatidylcholine liposome membrane

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• 作者：Toshinori  ; Shimanouchi¹ ; Makoto  ; Tasaki¹ ; Huong Thi  ; Vu¹ ; Haruyuki  ; Ishii¹ ; Noriko  ; Yoshimoto² ; Hiroshi  ; Umakoshi¹ ; Ryoichi  ; Kuboi¹ ;   ; ^{msb@cheng.es.osaka-u.ac.jp}
• 关键词：Alzheimer's disease ; Amyloid ¦Â/Cu Complex ; Cholesterol ; Domain ; Liposome
• 刊名：Journal of Bioscience and Bioengineering
• 出版年：2010
• 出版时间：February 2010
• 年：2010
• 卷：109
• 期：2
• 页码：145-148
• 全文大小：419 K

文摘

The amyloid ¦Â protein with 42 amino acid residues (A¦Â), which is a causative protein of Alzheimer's disease (AD), forms the complex with copper (II) to induce the cholesterol oxidase-like activity by the proton transfer from the cholesterol. In this study, the oxidation of cholesterol by A¦Â/Cu complex was investigated on the surface of the zwitterionic phospholipid liposome including the bound water advantageous for the enhancement of the proton transfer. The bound water was pooled by the formation of cholesterol-rich domain within liposomes. The resulting reactivity was enhanced by the proton transfer mediated by the bound water.