Lytton S D, Cabantchik Z I, Libman J, Shanzer A
Department of Biological Chemistry, Institute of Life Sciences, Hebrew University, Jerusalem, Israel.
Mol Pharmacol. 1991 Oct;40(4):584-90.
We introduce here a fluorescent derivative of desferrioxamine B (DFO) that retains the high affinity of the parent compound and displays a powerful inhibition of intraerythrocytic Plasmodium falciparum growth. NBD-DFO was synthesized by coupling 7-Nitrobenz-2-oxa-1,3-diazole (NBD) to the terminal amino group of DFO. The NBD group at this position renders the DFO molecule more lipophilic and imparts to it fluorescent properties. The novel NBD-DFO probe displays a unique combination of chemical and biological properties, such as 1) improved and selective permeation properties across membranes of P. falciparum-infected erythrocytes, 2) improved efficacy as an inhibitor of intraerythrocytic P. falciparum growth (including multidrug-resistant strains), 3) demonstrable Fe3+ scavenging within parasitized red cells, and 4) usefulness as a sensitive and versatile analytical tool for quantitative assessment of Fe3+ and for following iron-scavenging processes, because the fluorescence of NBD-DFO is demonstrably quenched upon complexation with Fe3+.
我们在此介绍一种去铁胺B(DFO)的荧光衍生物,它保留了母体化合物的高亲和力,并对红细胞内恶性疟原虫的生长表现出强大的抑制作用。NBD-DFO是通过将7-硝基苯并-2-恶唑-1,3-二唑(NBD)与DFO的末端氨基偶联而合成的。该位置的NBD基团使DFO分子更具亲脂性并赋予其荧光特性。新型NBD-DFO探针展现出化学和生物学特性的独特组合,例如:1)对恶性疟原虫感染红细胞膜具有改善的选择性渗透特性;2)作为红细胞内恶性疟原虫生长抑制剂(包括多重耐药菌株)的功效得到提高;3)在被寄生的红细胞内可证明有Fe3+清除作用;4)可用作定量评估Fe3+以及追踪铁清除过程的灵敏且通用的分析工具,因为NBD-DFO与Fe3+络合后其荧光明显淬灭。