Sastry M, Patel D J
Department of Biochemistry and Molecular Biophysics, College of Physicians and Surgeons, Columbia University, New York, New York 10032.
Biochemistry. 1993 Jul 6;32(26):6588-604. doi: 10.1021/bi00077a012.
We have characterized the NMR parameters for the complexes formed by the Mg(2+)-coordinated mithramycin dimer with self-complementary d(T-G-G-C-C-A) and d(T-C-G-C-G-A) duplexes. The solution structure of the latter complex has been determined using a combined NMR-molecular dynamics study including relaxation matrix refinement. The Mg(2+)-coordinated mithramycin dimer-d(T-C-G-C-G-A) complex exhibits a 2-fold center of symmetry with the divalent cation coordinated aglycons positioned opposite the central (G3-C4).(G3-C4) segment such that the aglycon C8 hydroxyl oxygens form symmetrical sequence-specific hydrogen bonds to guanine amino protons in the complex. The C-D-E trisaccharide segments of each monomer in the mithramycin dimer adopt extended conformations, are positioned inside the minor groove, and are directed toward either end of the duplex. The C-D saccharide component of one monomer and the aglycon of the other monomer in the mithramycin dimer share a widened minor groove with the hydrophobic edges of the C and D sugars interacting with individual strands of the duplex. The E-sugar ring is positioned in the floor of the minor groove, and its hydroxyl-bearing face interacts with both strands of the duplex through hydrogen-bonding and hydrophobic intermolecular interactions. The A-B disaccharide and the hydrophilic side chain form intermolecular contacts with the sugar-phosphate backbone in the complex. The antiparallel alignment of divalent cation coordinated monomers in the mithramycin dimer results in the two outwardly directed C-D-E trisaccharide segments generating a right-handed continuous hexasaccharide domain that spans six base pairs in the minor groove of the duplex. The solution structure of the mithramycin dimer-DNA complex reported in this study and the solution structure of the chromomycin dimer-DNA complex reported previously [Gao, X., Mirau, P., & Patel, D. J. (1992) J. Mol. Biol. 223, 259-279] show global similarities, as well as local differences that are of interest. All four nucleotides in the tetranucleotide segment of the duplex centered about the sequence-specific (G-C).(G-C) step adopt A-DNA sugar puckers and glycosidic torsion angles in the chromomycin dimer-DNA complex, while only the central cytidine adopts an A-DNA sugar pucker and glycosidic torsion angle in the mithramycin dimer-DNA complex.(ABSTRACT TRUNCATED AT 400 WORDS)
我们已对由镁离子配位的光神霉素二聚体与自身互补的d(T-G-G-C-C-A)和d(T-C-G-C-G-A)双链体形成的复合物的核磁共振参数进行了表征。通过包括弛豫矩阵精修在内的核磁共振-分子动力学联合研究,确定了后一种复合物的溶液结构。镁离子配位的光神霉素二聚体-d(T-C-G-C-G-A)复合物呈现出二重对称中心,二价阳离子配位的糖苷配基位于与中央(G3-C4).(G3-C4)片段相对的位置,使得糖苷配基的C8羟基氧与复合物中鸟嘌呤的氨基质子形成对称的序列特异性氢键。光神霉素二聚体中每个单体的C-D-E三糖片段呈伸展构象,位于小沟内部,并指向双链体的两端。光神霉素二聚体中一个单体的C-D糖组分和另一个单体的糖苷配基与双链体单链相互作用,共同占据一个变宽的小沟,其中C糖和D糖的疏水边缘与双链体的单链相互作用。E糖环位于小沟底部,其带有羟基的面通过氢键和疏水分子间相互作用与双链体的两条链相互作用。A-B二糖和亲水侧链在复合物中与糖-磷酸骨架形成分子间接触。光神霉素二聚体中二价阳离子配位单体的反平行排列导致两个向外的C-D-E三糖片段形成一个右手连续六糖结构域,该结构域跨越双链体小沟中的六个碱基对。本研究报道的光神霉素二聚体-DNA复合物的溶液结构与先前报道的嗜铬霉素二聚体-DNA复合物的溶液结构[Gao, X., Mirau, P., & Patel, D. J. (1992) J. Mol. Biol. 223, 259 - 279]显示出整体相似性以及有趣的局部差异。在嗜铬霉素二聚体-DNA复合物中,以序列特异性(G-C).(G-C)步为中心的双链体四核苷酸片段中的所有四个核苷酸均采用A-DNA糖构象和糖苷扭转角,而在光神霉素二聚体-DNA复合物中只有中央胞嘧啶采用A-DNA糖构象和糖苷扭转角。(摘要截取自400字)