丙基硒醚对过氧自由基诱导的蛋白质损伤的影响:官能团取代的影响

V. V. Gandhi, R. P. Das, B. Singh, A. Kunwar
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引用次数: 0

摘要

蛋白质是细胞功能的关键分子,也被认为对活性氧(ROS)诱导的氧化损伤非常敏感。本研究以线粒体为体外模型,研究了几种具有不同官能团但碳链(丙基)长度相似的简单水溶性脂肪族有机硒化合物对2,2 ' -偶氮-(2-氨基丙烷)二盐酸(AAPH)诱导的氧化损伤的保护作用。结果表明,APPH (20 mM)处理线粒体片段诱导蛋白质羰基化,导致氧化还原酶和电子传递链(ETC)失活,最终导致线粒体功能障碍。另一方面,0.5 mM单硒丁酸(SeBA)和单硒丙醇(SePOH)处理可显著阻止apph诱导的线粒体部分蛋白羰基化,恢复线粒体蛋白活性。相反,相同浓度的单硒丙基胺(SePAm)处理对aaph诱导的线粒体氧化损伤没有显著的保护作用。上述结果与报道的上述分子的过氧自由基破坏活性一致。综上所述,SeBA和SePOH是保护蛋白质免受氧化损伤的潜在候选分子,因此可以用于细胞模型中氧化应激的管理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Efficacy of propyl selenoethers against peroxyl radical induced protein damage: Effect of functional group substitution
Proteins are the critical molecules for cellular functionality and are also considered to be highly susceptible for reactive oxygen species (ROS)-induced oxidative damages. The present study was aimed to evaluate some simple water soluble aliphatic organoselenium compounds bearing different functional groups but of similar carbon chain (propyl) length for protective effect against 2,2’-azobis-(2-amidinopropane) dihydrochloride (AAPH)-induced oxidative damage using mitochondria as an in vitro model. The results indicated that APPH (20 mM) treatment of mitochondrial fraction induced protein carbonylation leading to inactivation of redox enzymes and electron transport chain (ETC) and ultimately the mitochondrial dysfunction. On the other hand, treatment with 0.5 mM of monoselenobutyric acid (SeBA) and monoselenopropyl alcohol (SePOH) significantly prevented APPH-induced protein carbonylation in mitochondrial fraction and restored activities of mitochondrial proteins. On contrary, monoselenopropyl amine (SePAm) treatment at identical concentration did not show significant protection to mitochondrial activity from AAPH-induced oxidative damages. Above results are in concurrence to the reported peroxyl radical savaging activities of above molecules. In conclusion, SeBA and SePOH are potential candidate molecules to protect proteins from oxidative damages and therefore can be useful for management of oxidative stress in cellular models.
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来源期刊
Current Chemical Biology
Current Chemical Biology Medicine-Biochemistry (medical)
CiteScore
1.40
自引率
0.00%
发文量
16
期刊介绍: Current Chemical Biology aims to publish full-length and mini reviews on exciting new developments at the chemistry-biology interface, covering topics relating to Chemical Synthesis, Science at Chemistry-Biology Interface and Chemical Mechanisms of Biological Systems. Current Chemical Biology covers the following areas: Chemical Synthesis (Syntheses of biologically important macromolecules including proteins, polypeptides, oligonucleotides, oligosaccharides etc.; Asymmetric synthesis; Combinatorial synthesis; Diversity-oriented synthesis; Template-directed synthesis; Biomimetic synthesis; Solid phase biomolecular synthesis; Synthesis of small biomolecules: amino acids, peptides, lipids, carbohydrates and nucleosides; and Natural product synthesis).
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