Soskić Vukić, Groebe Karlfried, Schrattenholz André
ProteoSys AG, Mainz, Germany.
Exp Gerontol. 2008 Apr;43(4):247-57. doi: 10.1016/j.exger.2007.12.001. Epub 2007 Dec 14.
One of the most fundamental molecular aspects of aging is accumulating oxidative damage caused by reactive oxygen species (ROS) as proposed by the free radical theory of aging. These unwanted chemical side products of normal metabolism lead to the formation of altered, less active and potentially toxic species of DNA, RNA, proteins, lipids, and small molecules. Due to gradually accumulating small contributions of irreversible reactions during ageing, uncatalyzed chemical side reactions occur with increasing frequencies and repair functions decline. Eventually key biochemical pathways are impaired by increasingly less efficient cellular stress management. In this review, we describe the chemical nature of nonenzymatic age-related modifications of proteins and provide an overview of related analytical challenges and approaches, with a focus on mass spectrometry. We include the description of a strategy to rapidly exploit the wealth of mass spectrometric information from standard MALDI-TOF peptide fingerprints for the characterisation of age-related oxidative amino acid modifications.
衰老最基本的分子层面之一是,如衰老自由基理论所提出的,活性氧(ROS)导致的氧化损伤不断积累。正常新陈代谢中这些有害的化学副产物会导致DNA、RNA、蛋白质、脂质和小分子发生改变、活性降低并产生潜在毒性。由于衰老过程中不可逆反应的微小贡献逐渐积累,未催化的化学副反应发生频率增加,修复功能下降。最终,关键生化途径因细胞应激管理效率越来越低而受损。在本综述中,我们描述了蛋白质非酶促年龄相关修饰的化学性质,并概述了相关的分析挑战和方法,重点是质谱分析。我们还介绍了一种策略,可快速利用标准基质辅助激光解吸电离飞行时间(MALDI-TOF)肽指纹图谱中的大量质谱信息,来表征与年龄相关的氧化氨基酸修饰。