Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892, USA.
Int J Mol Sci. 2024 Apr 29;25(9):4852. doi: 10.3390/ijms25094852.
Iron regulatory proteins (IRP1 and IRP2) are the master regulators of mammalian iron homeostasis. They bind to the iron-responsive elements (IREs) of the transcripts of iron-related genes to regulate their expression, thereby maintaining cellular iron availability. The primary method to measure the IRE-binding activity of IRPs is the electrophoresis mobility shift assay (EMSA). This method is particularly useful for evaluating IRP1 activity, since IRP1 is a bifunctional enzyme and its protein levels remain similar during conversion between the IRE-binding protein and cytosolic aconitase forms. Here, we exploited a method of using a biotinylated-IRE probe to separate IRE-binding IRPs followed by immunoblotting to analyze the IRE-binding activity. This method allows for the successful measurement of IRP activity in cultured cells and mouse tissues under various iron conditions. By separating IRE-binding IRPs from the rest of the lysates, this method increases the specificity of IRP antibodies and verifies whether a band represents an IRP, thereby revealing some previously unrecognized information about IRPs. With this method, we showed that the S711-phosphorylated IRP1 was found only in the IRE-binding form in PMA-treated Hep3B cells. Second, we found a truncated IRE-binding IRP2 isoform that is generated by proteolytic cleavage on sites in the 73aa insert region of the IRP2 protein. Third, we found that higher levels of SDS, compared to 1-2% SDS in regular loading buffer, could dramatically increase the band intensity of IRPs in immunoblots, especially in HL-60 cells. Fourth, we found that the addition of SDS or LDS to cell lysates activated protein degradation at 37 °C or room temperature, especially in HL-60 cell lysates. As this method is more practical, sensitive, and cost-effective, we believe that its application will enhance future research on iron regulation and metabolism.
铁调节蛋白(IRP1 和 IRP2)是哺乳动物铁稳态的主要调节剂。它们与铁相关基因的转录物中的铁反应元件(IRE)结合,以调节其表达,从而维持细胞内铁的可用性。测量 IRP 的 IRE 结合活性的主要方法是电泳迁移率变动分析(EMSA)。该方法对于评估 IRP1 活性特别有用,因为 IRP1 是一种双功能酶,其在 IRE 结合蛋白和胞质 aconitase 形式之间转换时,其蛋白水平保持相似。在这里,我们利用一种使用生物素化-IRE 探针分离 IRE 结合 IRP 然后进行免疫印迹分析 IRE 结合活性的方法。该方法允许在各种铁条件下成功测量培养细胞和小鼠组织中的 IRP 活性。通过将 IRE 结合的 IRP 与其余的裂解物分离,该方法增加了 IRP 抗体的特异性,并验证了条带是否代表 IRP,从而揭示了一些关于 IRP 的先前未被认识的信息。使用这种方法,我们表明,在 PMA 处理的 Hep3B 细胞中,只有 S711 磷酸化的 IRP1 才存在于 IRE 结合形式中。其次,我们发现了一种截断的 IRE 结合 IRP2 同工型,它是由 IRP2 蛋白 73aa 插入区域中的位点的蛋白水解切割产生的。第三,我们发现与常规加载缓冲液中的 1-2%SDS 相比,更高浓度的 SDS(如 1-2%SDS)可显著增加免疫印迹中 IRP 的条带强度,尤其是在 HL-60 细胞中。第四,我们发现 SDS 或 LDS 加入细胞裂解液会在 37°C 或室温下激活蛋白降解,尤其是在 HL-60 细胞裂解液中。由于这种方法更实用、更敏感、更具成本效益,我们相信它的应用将增强未来对铁调节和代谢的研究。