Lavery R, Zakrzewska K, Pullman B
Institut de Biologie Physico-Chimique, Laboratoire de Biochimie Théorique associé au C.N.R.S., Paris, France.
J Biomol Struct Dyn. 1986 Jun;3(6):1155-70. doi: 10.1080/07391102.1986.10508492.
A detailed theoretical study has been made for five antibiotics which all bind selectively to AT sequences in the minor groove of B-DNA: SN-18071, NSC-101327, distamycin-2, distamycin-3 and netropsin. The optimal complexes were found for systems in which the flexibility of DNA, as well as that of the antibiotics, was taken into account. Explicit, mobile counterions and a dielectric function modelling aqueous solution were also included. The binding geometries of the most strongly interacting antibiotics, distamycin-3 and netropsin, are compared in considerable detail and it is shown that notable differences exist between them. The results for netropsin are also discussed in the light of recent disagreements concerning its exact binding location within DNA.
对五种均能选择性结合到B-DNA小沟中AT序列的抗生素进行了详细的理论研究:SN-18071、NSC-101327、偏端霉素-2、偏端霉素-3和纺锤菌素。对于考虑了DNA以及抗生素柔韧性的体系,找到了最优复合物。还包括明确的可移动抗衡离子和模拟水溶液的介电函数。对相互作用最强的抗生素偏端霉素-3和纺锤菌素的结合几何结构进行了相当详细的比较,结果表明它们之间存在显著差异。还根据最近关于纺锤菌素在DNA中确切结合位置的分歧对其结果进行了讨论。