Weissbach Herbert, Resnick Lionel, Brot Nathan
Center for Molecular Biology and Biotechnology, Florida Atlantic University, 777 Glades Road, Boca Raton, FL 33431, USA.
Biochim Biophys Acta. 2005 Jan 17;1703(2):203-12. doi: 10.1016/j.bbapap.2004.10.004. Epub 2004 Nov 11.
An enzyme that can reduce methionine sulfoxide in proteins was first discovered in Escherichia coli about 25 years ago. It is now apparent that there is a family of enzymes, referred to as methionine sulfoxide reductases (Msr), and in recent years there has been considerable interest in one of the members of the Msr family, MsrA. This enzyme has been shown to protect cells against oxidative damage, which suggests a possible role in a large number of age-related diseases. This review summarizes the history of the discovery of MsrA, properties of the enzyme and its role in protecting cells against oxidative damage. Other members of the Msr family that differ in substrate specificity and localization are described as well as a possible role for the Msr system in drug metabolism. The concept that the Msr system can be used to develop novel drugs that could be catalytic anti-oxidants is discussed.
大约25年前,在大肠杆菌中首次发现了一种能够还原蛋白质中甲硫氨酸亚砜的酶。现在很明显,存在一个酶家族,称为甲硫氨酸亚砜还原酶(Msr),近年来,Msr家族的一个成员MsrA引起了人们的极大兴趣。这种酶已被证明可以保护细胞免受氧化损伤,这表明它在大量与年龄相关的疾病中可能发挥作用。这篇综述总结了MsrA的发现历史、该酶的特性及其在保护细胞免受氧化损伤中的作用。还描述了Msr家族中底物特异性和定位不同的其他成员,以及Msr系统在药物代谢中的可能作用。讨论了Msr系统可用于开发新型药物(即催化抗氧化剂)的概念。