Velu Chinavenmeni S, Niture Suryakant K, Doneanu Catalin E, Pattabiraman Nagarajan, Srivenugopal Kalkunte S
Anticancer Resistance Research Group, Department of Pharmaceutical Sciences, Texas Tech University Health Sciences Center, Amarillo, Texas 79106, USA.
Biochemistry. 2007 Jul 3;46(26):7765-80. doi: 10.1021/bi700425y. Epub 2007 Jun 8.
The cellular mechanisms that modulate the redox state of p53 tumor suppressor remain unclear, although its DNA binding function is known to be strongly inhibited by oxidative and nitrosative stresses. We show that human p53 is subjected to a new and reversible posttranslational modification, namely, S-glutathionylation in stressed states, including DNA damage. First, a rapid and direct incorporation of biotinylated GSH or GSSG into the purified recombinant p53 protein was observed. The modified p53 had a significantly weakened ability to bind its consensus DNA sequence. Reciprocal immunoprecipitations and a GST overlay assay showed that p53 in tumor cells was marginally glutathionylated; however, the level of modification increased greatly after oxidant and DNA-damaging treatments. GSH modification coexisted with the serine phophorylations in activated p53, and the thiol-conjugated protein was present in nuclei. When tumor cells treated with camptothecin or cisplatin were subsequently exposed to glutathione-enhancing agents, p53 underwent dethiolation accompanied by detectable increases in the level of p21waf1 expression, relative to the DNA-damaging drugs alone. Mass spectrometry of GSH-modified p53 protein identified cysteines 124, 141, and 182, all present in the proximal DNA-binding domain, as the sites of glutathionylation. Biotinylated maleimide also reacted rapidly with Cys141, implying that this is the most reactive cysteine on the p53 surface. The glutathionylatable cysteines were found to exist in a negatively charged microenvironment in cellular p53. Molecular modeling studies located Cys124 and -141 at the dimer interface of p53 and showed glutathionylation of either residue would inhibit p53-DNA association and also interfere with protein dimerization. These results show for the first time that shielding of reactive cysteines contributes to a negative regulation for human p53 and imply that such an inactivation of the transcription factor may represent an acute defensive response with significant consequences for oncogenesis.
尽管已知p53肿瘤抑制因子的DNA结合功能会受到氧化应激和亚硝化应激的强烈抑制,但其调节p53氧化还原状态的细胞机制仍不清楚。我们发现,在包括DNA损伤在内的应激状态下,人类p53会发生一种新的、可逆的翻译后修饰,即S-谷胱甘肽化修饰。首先,观察到生物素化的谷胱甘肽(GSH)或氧化型谷胱甘肽(GSSG)能快速、直接地掺入纯化的重组p53蛋白中。修饰后的p53与共有DNA序列结合的能力显著减弱。相互免疫沉淀和GST覆盖分析表明,肿瘤细胞中的p53仅有少量谷胱甘肽化修饰;然而,在氧化剂和DNA损伤处理后,修饰水平大幅增加。谷胱甘肽化修饰与激活的p53中的丝氨酸磷酸化共存,且硫醇共轭蛋白存在于细胞核中。当用喜树碱或顺铂处理后的肿瘤细胞随后暴露于增强谷胱甘肽的试剂时,相对于单独使用DNA损伤药物,p53发生了脱巯基化,同时p21waf1表达水平显著升高。对谷胱甘肽化修饰的p53蛋白进行质谱分析,确定半胱氨酸124、141和182(均位于近端DNA结合结构域)为谷胱甘肽化修饰位点。生物素化马来酰亚胺也能与半胱氨酸141快速反应,这表明该位点是p53表面反应活性最高的半胱氨酸。研究发现,可谷胱甘肽化修饰的半胱氨酸在细胞内p53中处于带负电荷的微环境中。分子模型研究表明,半胱氨酸124和141位于p53的二聚体界面,任何一个位点的谷胱甘肽化修饰都会抑制p53与DNA的结合,也会干扰蛋白质二聚化。这些结果首次表明,对反应性半胱氨酸的屏蔽作用对人类p53起到负调控作用,这意味着转录因子的这种失活可能代表一种急性防御反应,对肿瘤发生具有重大影响。