Department of Chemistry, National Institute of Technology, Rourkela, Odisha, India.
Methods Mol Biol. 2023;2671:121-134. doi: 10.1007/978-1-0716-3222-2_7.
Understanding the iron accumulation process in ferritin protein nanocages has remained a centerpiece in the field of iron biochemistry/biomineralization, which ultimately has implications in health and diseases. Although mechanistic differences of iron acquisition and mineralization exist in the superfamily of ferritins, we describe the techniques that can be used to investigate the accumulation of iron in all the ferritin proteins by in vitro iron mineralization process. In this chapter, we report that the non-denaturing polyacrylamide gel electrophoresis coupled with Prussian blue staining (in-gel assay) can be useful to investigate the iron-loading efficiency in ferritin protein nanocage, by estimating the relative amount of iron incorporated inside it. Similarly, the absolute size of the iron mineral core and the amount of total iron accumulated inside its nanocavity can be determined by using transmission electron microscopy and spectrophotometry, respectively.
了解铁蛋白纳米笼中铁的积累过程一直是铁生物化学/生物矿化领域的核心内容,这对健康和疾病都有影响。尽管在铁蛋白超家族中存在铁摄取和矿化的机制差异,但我们描述了可用于通过体外矿化过程研究所有铁蛋白中铁积累的技术。在本章中,我们报告了非变性聚丙烯酰胺凝胶电泳结合普鲁士蓝染色(胶内测定)可用于通过估计其内部结合的铁的相对量来研究铁蛋白纳米笼中铁的加载效率。同样,也可以使用透射电子显微镜和分光光度法分别确定铁矿物核心的绝对大小和其纳米腔室内积累的总铁量。