DNA sequence recognition by a novel series of minor groove-binding ligands.

Anti-cancer drug design Pub Date : 1999-06-01
K R Fox, Y Yan, B Gong
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Abstract

We have used quantitative DNase I and hydroxyl radical footprinting with three DNA fragments to examine the sequence-specific recognition of DNA by five novel minor groove-binding ligands which contain a structural motif in which a para-disubstituted benzene ring is flanked by two meta-disubstituted benzene rings. The compounds are all AT-selective and bind better to (AT)6 than (AT)4 sites. The ligands bind more tightly to AATT and TAAT than TTAA, TATA and ATAT, and avoid sequences containing central TpA steps. Different side groups cause subtle changes to the sequence recognition properties of these ligands.

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一系列新的次要凹槽结合配体识别DNA序列。
我们使用定量DNA酶I和羟基自由基足迹与三个DNA片段来检查DNA序列特异性识别的五个新的小凹槽结合配体,其中包含一个结构基序,其中一个对二取代苯环两侧是两个间二取代苯环。这些化合物都具有AT选择性,并且与AT 6位点的结合优于AT 4位点。与TTAA、TATA和ATAT相比,这些配体与AATT和TAAT的结合更紧密,并且避免了含有中心TpA步骤的序列。不同的侧基引起这些配体序列识别特性的细微变化。
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