...
首页> 外文期刊>The Biochemical Journal >The carbonylation and covalent dimerization of human superoxide dismutase 1 caused by its bicarbonate-dependent peroxidase activity is inhibited by the radical scavenger tempol.
【24h】

The carbonylation and covalent dimerization of human superoxide dismutase 1 caused by its bicarbonate-dependent peroxidase activity is inhibited by the radical scavenger tempol.

机译:自由基清除剂tempol抑制了人超氧化物歧化酶1的碳酸氢盐依赖性过氧化物酶活性引起的羰基化和共价二聚。

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Tempol (4-hydroxy-2,2,6,6-tetramethyl piperidine-1-oxyl) reduces tissue injury in animal models of various diseases via mechanisms that are not completely understood. Recently, we reported that high doses of tempol moderately increased survival in a rat model of ALS (amyotrophic lateral sclerosis) while decreasing the levels of oxidized hSOD1 (human Cu,Zn-superoxide dismutase) in spinal cord tissues. To better understand such a protective effect invivo, we studied the effects of tempol on hSOD1 oxidation invitro. The chosen oxidizing system was the bicarbonate-dependent peroxidase activity of hSOD1 that consumes H2O2 to produce carbonate radical, which oxidizes the enzyme. Most of the experiments were performed with 30muM hSOD1, 25mM bicarbonate, 1mM H2O2, 0.1mM DTPA (diethylenetriaminepenta-acetic acid) and 50mM phosphate buffer at a final pH of 7.4. The results showed that tempol (5-75muM) does not inhibit hSOD1 turnover, but decreases its resulting oxidation to carbonylated and covalently dimerized forms. Tempol acted by scavenging the carbonate radical produced and by recombining with hSOD1-derived radicals. As a result, tempol was consumed nearly stoichiometrically with hSOD1 monomers. MS analyses of turned-over hSOD1 and of a related peptide oxidized by the carbonate radical indicated the formation of a relatively unstable adduct between tempol and hSOD1-Trp32*. Tempol consumption by the bicarbonate-dependent peroxidase activity of hSOD1 may be one of the reasons why high doses of tempol were required to afford protection in an ALS rat model. Overall, the results of the present study confirm that tempol can protect against protein oxidation and the ensuing consequences.Registry Number/Name of Substance 0 (Bicarbonates). 0 (Cyclic N-Oxides). 0 (Free Radical Scavengers). 0 (Free Radicals). 0 (Peptides). 0 (Recombinant Proteins). 0 (Spin Labels). 2226-96-2 (tempol). 7722-84-1 (Hydrogen Peroxide). EC 1-11-1 (Peroxidases). EC 1-15-1 (superoxide dismutase 1). EC 1-15-1-1 (Superoxide Dismutase).
机译:Tempol(4-羟基-2,2,6,6-四甲基哌啶-1-氧基)可通过尚未完全了解的机制减轻各种疾病动物模型中的组织损伤。最近,我们报道了高剂量的tempol在ALS(肌萎缩性侧索硬化)大鼠模型中适度增加了存活率,同时降低了脊髓组织中氧化的hSOD1(人类Cu,Zn-超氧化物歧化酶)的水平。为了更好地了解这种体内保护作用,我们研究了tempol对hSOD1氧化体外的影响。选择的氧化系统是hSOD1的依赖于碳酸氢盐的过氧化物酶活性,该酶消耗H2O2产生碳酸根自由基,从而氧化该酶。大多数实验是使用30μMhSOD1、25mM碳酸氢盐,1mM H2O2、0.1mM DTPA(二亚乙基三胺五乙酸)和50mM磷酸盐缓冲液进行的,最终pH值为7.4。结果表明,tempol(5-75μM)不会抑制hSOD1转换,但会降低其氧化成羰基化和共价二聚的形式。 Tempol通过清除产生的碳酸盐自由基并与hSOD1衍生的自由基重组来发挥作用。结果,hSOD1单体几乎以化学计量消耗了tempol。质谱分析了经过转换的hSOD1和被碳酸盐自由基氧化的相关肽,表明在tempol和hSOD1-Trp32 *之间形成了相对不稳定的加合物。 hSOD1依赖于碳酸氢盐的过氧化物酶活性消耗的tempol可能是需要高剂量的tempol才能在ALS大鼠模型中提供保护的原因之一。总的来说,本研究的结果证实了tempol可以防止蛋白质氧化和随之而来的后果。登记号/物质0的名称(碳酸氢盐)。 0(循环氮氧化物)。 0(自由基清除剂)。 0(自由基)。 0(肽)。 0(重组蛋白)。 0(旋转标签)。 2226-96-2(tempol)。 7722-84-1(过氧化氢)。 EC 1-11-1(过氧化物酶)。 EC 1-15-1(超氧化物歧化酶1)。 EC 1-15-1-1(超氧化物歧化酶)。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号