Comer Jonathan M, Zhang Li
Department of Biological Sciences, School of Natural Sciences and Mathematics, The University of Texas at Dallas, Richardson, TX 75080, USA.
Cells. 2018 May 24;7(6):47. doi: 10.3390/cells7060047.
The study of heme is important to our understanding of cellular bioenergetics, especially in cancer cells. The function of heme as a prosthetic group in proteins such as cytochromes is now well-documented. Less is known, however, about its role as a regulator of metabolic and energetic pathways. This is due in part to some inherent difficulties in studying heme. Due to its slightly amphiphilic nature, heme is a "sticky" molecule which can easily bind non-specifically to proteins. In addition, heme tends to dimerize, oxidize, and aggregate in purely aqueous solutions; therefore, there are constraints on buffer composition and concentrations. Despite these difficulties, our knowledge of heme's regulatory role continues to grow. This review sums up the latest methods used to study reversible heme binding. Heme-regulated proteins will also be reviewed, as well as a system for imaging the cellular localization of heme.
对血红素的研究对于我们理解细胞生物能量学非常重要,尤其是在癌细胞中。血红素作为细胞色素等蛋白质中的辅基的功能现已得到充分证明。然而,关于其作为代谢和能量途径调节剂的作用,我们了解得较少。这部分是由于研究血红素存在一些固有困难。由于其略带两亲性的性质,血红素是一种“粘性”分子,很容易与蛋白质非特异性结合。此外,血红素在纯水溶液中容易二聚化、氧化和聚集;因此,对缓冲液的组成和浓度有限制。尽管存在这些困难,我们对血红素调节作用的认识仍在不断增加。本综述总结了用于研究可逆血红素结合的最新方法。还将对血红素调节蛋白以及血红素细胞定位成像系统进行综述。