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通过使用合成CD36肽交联板的检测方法,进一步验证不饱和长链脂肪酸作为氧化低密度脂蛋白与CD36结合的抑制剂。

Further validation of unsaturated long-chain fatty acids as inhibitors for oxidized low-density lipoprotein binding to CD36 via assays with synthetic CD36 peptide-cross-linked plates.

作者信息

Kozai Yuki, Tsuzuki Satoshi, Takai Marie, Eguchi Ai, Matsumura Shigenobu, Inoue Kazuo, Fushiki Tohru

机构信息

a Laboratory of Nutrition Chemistry, Division of Food Science and Biotechnology , Graduate School of Agriculture, Kyoto University , Kyoto , Japan.

出版信息

Biosci Biotechnol Biochem. 2014;78(5):839-42. doi: 10.1080/09168451.2014.891934. Epub 2014 Jun 13.

Abstract

We recently obtained evidence that unsaturated long-chain fatty acids (LCFAs) (e.g. oleic acid) inhibit binding of oxidized low-density lipoproteins (oxLDLs) to CD36. In the present study, we validated this prediction by examining inhibition by unsaturated LCFAs of Alexa-fluor-labeled oxLDL binding to multiwell plates onto which a synthetic CD36 peptide is covalently immobilized via thiol-maleimide coupling.

摘要

我们最近获得的证据表明,不饱和长链脂肪酸(LCFAs)(如油酸)可抑制氧化型低密度脂蛋白(oxLDLs)与CD36的结合。在本研究中,我们通过检测不饱和LCFAs对Alexa荧光标记的oxLDL与通过硫醇-马来酰亚胺偶联共价固定有合成CD36肽的多孔板结合的抑制作用,验证了这一预测。

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