Buckett Peter D, Wessling-Resnick Marianne
Harvard School of Public Health, Department of Genetics and Complex Diseases, 665 Huntington Ave., Boston, MA 02115, USA.
Am J Physiol Gastrointest Liver Physiol. 2009 Apr;296(4):G798-804. doi: 10.1152/ajpgi.90342.2008. Epub 2009 Jan 29.
Divalent metal transporter-1 (DMT1) is a divalent cation transporter that plays a key role in iron metabolism by mediating ferrous iron uptake across the small intestine. We have previously identified several small molecule inhibitors of iron uptake (4). Using a cell line that stably overexpresses DMT1, we screened the ability of these inhibitors to specifically block this transporter's activity. One compound, NSC306711, inhibited DMT1-mediated iron uptake in a reversible and competitive manner. This inhibitor is a polysulfonated dye containing two copper centers. Although one of these two sites could be chelated by Triethylenetetramine copper chelation did not perturb NSC306711 inhibition of DMT1 activity. Several other polysulfonated dyes with structural features similar to NSC306711 were identified as potential DMT1 transport inhibitors. This study characterizes important pharmacological tools that can be used to probe DMT1's mechanism of iron transport and its role in iron metabolism.
二价金属转运蛋白1(DMT1)是一种二价阳离子转运蛋白,通过介导亚铁在小肠的吸收,在铁代谢中发挥关键作用。我们之前已鉴定出几种铁吸收的小分子抑制剂(4)。利用稳定过表达DMT1的细胞系,我们筛选了这些抑制剂特异性阻断该转运蛋白活性的能力。一种化合物NSC306711以可逆且竞争性的方式抑制DMT1介导的铁吸收。该抑制剂是一种含有两个铜中心的多磺酸化染料。虽然这两个位点之一可被三亚乙基四胺螯合,但铜螯合并不干扰NSC306711对DMT1活性的抑制。其他几种具有与NSC306711相似结构特征的多磺酸化染料被鉴定为潜在的DMT1转运抑制剂。本研究表征了可用于探究DMT1铁转运机制及其在铁代谢中作用的重要药理学工具。