Exner M, Hermann M, Hofbauer R, Hartmann B, Kapiotis S, Gmeiner B
Department of Laboratory Medicine, University of Vienna, Vienna, Austria.
FEBS Lett. 2002 Nov 20;531(3):402-6. doi: 10.1016/s0014-5793(02)03571-8.
Ceruloplasmin (CP) oxidises low density lipoprotein (LDL). The oxidising potential depends on the formation of Cu(+)-CP which is redox-cycled during oxidation. Homocysteine (HCY) reduces free Cu(2+), potentiating its cell-damaging property. We show that HCY enhanced LDL oxidation by CP, but did not activate the LDL oxidising potential of Cu(2+)-diamine oxidase. Selective removal of the redox-active Cu(2+) abolished the LDL oxidase activity of CP. However, HCY partially restored the LDL oxidase activity of redox-copper depleted CP, indicating that the remaining six copper atoms in CP may also be involved in the process. Spectroscopic and oxidation inhibition studies using the Cu(+)-reagent bathocuproine revealed that HCY induced Cu(+)-CP formation, thus promoting its LDL oxidase activity.
铜蓝蛋白(CP)可氧化低密度脂蛋白(LDL)。其氧化电位取决于Cu(+)-CP的形成,Cu(+)-CP在氧化过程中进行氧化还原循环。同型半胱氨酸(HCY)可还原游离Cu(2+),增强其细胞损伤特性。我们发现,HCY可增强CP对LDL的氧化作用,但不会激活Cu(2+)-二胺氧化酶的LDL氧化电位。选择性去除具有氧化还原活性的Cu(2+)可消除CP的LDL氧化酶活性。然而,HCY可部分恢复氧化还原铜耗尽的CP的LDL氧化酶活性,这表明CP中剩余的六个铜原子可能也参与了该过程。使用Cu(+)试剂bathocuproine进行的光谱和氧化抑制研究表明,HCY可诱导Cu(+)-CP的形成,从而促进其LDL氧化酶活性。