Università Vita-Salute, Division of Genetics and Cell Biology, San Raffaele Scientific Institute, Milano, Italy.
FEBS Lett. 2010 Jul 16;584(14):2995-8. doi: 10.1016/j.febslet.2010.05.055. Epub 2010 May 31.
Oxidative protein folding in the luminal compartment of the endoplasmic reticulum is thought to be mediated by a proteinaceous electron relay system composed by PDI and ER oxidoreductin 1 (Ero1), transferring electrons from the cysteinyl residues of substrate proteins to oxygen. However, recent observations revealed that Ero1 isoforms are dispensable. Endoplasmic reticulum is known as a generator and accumulator of low molecular weight oxidants; some of them have already been shown to promote oxidative folding. On the basis of these observations a new theory of oxidative folding is proposed where the oxidative power is provided by the stochastic contribution of prooxidants.
内质网腔中氧化的蛋白质折叠被认为是由 PD I 和内质网氧化还原酶 1 (Ero1) 组成的蛋白质电子中继系统介导的,该系统将电子从底物蛋白的半胱氨酸残基转移到氧上。然而,最近的观察结果表明 Ero1 同工型是可有可无的。内质网是已知的低分子量氧化剂的产生者和积累者;其中一些已经被证明可以促进氧化折叠。基于这些观察结果,提出了一种新的氧化折叠理论,其中氧化能力是由促氧化剂的随机贡献提供的。