Molecular targets of oxidative stress

被引:327
作者
Avery, Simon V. [1 ]
机构
[1] Univ Nottingham, Sch Biol, Nottingham NG7 2RD, England
基金
英国自然环境研究理事会; 英国生物技术与生命科学研究理事会;
关键词
actin; iron-sulfur cluster; lipid peroxidation; mistranslation; protein aggregation; protein oxidation; BASE EXCISION-REPAIR; ESCHERICHIA-COLI; DNA-DAMAGE; SACCHAROMYCES-CEREVISIAE; HYDROGEN-PEROXIDE; CELL-DEATH; GLYCERALDEHYDE-3-PHOSPHATE DEHYDROGENASE; LIPID-PEROXIDATION; PROTEIN DAMAGE; HELICOBACTER-PYLORI;
D O I
10.1042/BJ20101695
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Aerobic life requires organisms to resist the damaging effects of ROS (reactive oxygen species), particularly during stress. Extensive research has established a detailed picture of how cells respond to oxidative stress. Attention is now focusing on identifying the key molecular targets of ROS, which cause killing when resistance is overwhelmed. Experimental criteria used to establish such targets have differing merits. Depending on the nature of the stress, ROS cause loss of essential cellular functions or gain of toxic functions. Essential targets on which life pivots during ROS stress include membrane lipid integrity and activity of ROS-susceptible proteins, including proteins required for faithful translation of mRNA. Protein oxidation also triggers accumulation of toxic protein aggregates or induction of apoptotic cell death. This burgeoning understanding of the principal ROS targets will offer new possibilities for therapy of ROS related diseases.
引用
收藏
页码:201 / 210
页数:10
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