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双层嵌入酞菁 4 对心磷脂和细胞色素 c 的光氧化作用。

Photo-oxidation of cardiolipin and cytochrome c with bilayer-embedded Pc 4.

机构信息

Department of Biochemistry, Western Reserve University School of Medicine, Cleveland, OH 44106, USA.

出版信息

Free Radic Biol Med. 2010 Sep 1;49(5):718-25. doi: 10.1016/j.freeradbiomed.2010.05.014. Epub 2010 May 25.

Abstract

Singlet oxygen, (1)O(2), is produced by absorption of red light by the phthalocyanine dye Pc 4, followed by energy transfer to dissolved triplet molecular oxygen, (3)O(2). In tissues, Pc 4 concentrates in lipid bilayers, and particularly in mitochondrial membranes, because of its positive charge. Illumination of cells and tissues with red light after uptake of Pc 4 results in cell death. The potential initial chemical steps that result in cellular dysfunction have been characterized in this study. Both unsaturated acyl chains of phospholipids and proteins are identified as targets of oxidation. Tetra-linoleoyl cardiolipin was oxidized in both liposomes and mitochondria after Pc 4-mediated (1)O(2) generation. Evidence for the formation of both mono- and bis-hydroperoxide adducts of single linoleoyl side chains is provided by ESI-MS and ESI-MS/MS. Similarly, illumination of Pc 4 in liposomes and mitochondria resulted in cytochrome c oxidation as detected by oxidation of His 26 in the peptide H(26)*KTGPNLHGLFGK, further supporting the potential use of this peptide as a biomarker for the presence of mitochondrial oxidative stress characteristic of (1)O(2) in vivo (J. Kim et al., Free Radic. Biol. Med. 44:1700-1711; 2008). These observations provide evidence that formation of lipid hydroperoxides and/or protein oxidation can be the initial chemical steps in Pc 4-mediated induction of apoptosis in photodynamic therapy.

摘要

单线态氧,(1)O(2),是通过酞菁染料 Pc 4 吸收红光产生的,然后能量转移到溶解的三重态分子氧,(3)O(2)。在组织中,由于正电荷,Pc 4 集中在脂质双层中,特别是在线粒体膜中。在摄取 Pc 4 后用红光照射细胞和组织会导致细胞死亡。本研究已经描述了导致细胞功能障碍的潜在初始化学步骤。磷脂和蛋白质的不饱和酰基链都被确定为氧化的靶标。在 Pc 4 介导的(1)O(2)生成后,四-亚油酰心磷脂在脂质体和线粒体中都被氧化。ESI-MS 和 ESI-MS/MS 提供了形成单亚油酸侧链的单过氧化物和双过氧化物加合物的证据。同样,在脂质体和线粒体中照射 Pc 4 导致细胞色素 c 氧化,如肽 H(26)*KTGPNLHGLFGK 中 His 26 的氧化所检测到的,这进一步支持了该肽作为体内(1)O(2)存在的线粒体氧化应激标志物的潜在用途(J. Kim 等人,自由基生物学与医学 44:1700-1711; 2008)。这些观察结果提供了证据,表明脂质过氧化物的形成和/或蛋白质氧化可能是光动力疗法中 Pc 4 介导的细胞凋亡诱导的初始化学步骤。

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