Hammer B C, Russell R A, Warrener R N, Collins J G
Department of Chemistry, University College, University of New South Wales, Australian Defence Force Academy, Canberra.
Biochem Int. 1991 Aug;24(6):1075-84.
The nucleotide binding ability of the novel anthracycline drug, 3-fluoro-4-demethoxydaunomycin, has been studied by two dimensional 1H NMR correlated spectroscopy (COSY). In the COSY spectrum of the nucleotide mini-helix d(CTGCAG)2 cross-peaks are observed from the spin-coupled H6 and H5 protons of the cytidine bases. Additional cytidine H6/H5 cross-peaks are observed in the COSY spectrum of the anthracycline-d(CTGCAG)2 complex. These additional cytidine cross-peaks enable the identification of the anthracycline binding sites and the determination of the relative kinetic stability of the bound drug at each binding site.
新型蒽环类药物3-氟-4-去甲氧基柔红霉素的核苷酸结合能力已通过二维1H NMR相关光谱法(COSY)进行了研究。在核苷酸小螺旋d(CTGCAG)2的COSY谱中,观察到了来自胞嘧啶碱基自旋耦合的H6和H5质子的交叉峰。在蒽环类药物-d(CTGCAG)2复合物的COSY谱中还观察到了额外的胞嘧啶H6/H5交叉峰。这些额外的胞嘧啶交叉峰能够确定蒽环类药物的结合位点,并测定结合药物在每个结合位点的相对动力学稳定性。