Samuelson P, Jansen K, Kubista M
Department of Biochemistry and Biophysics, Chalmers University of Technology, Gothenburg, Sweden.
J Mol Recognit. 1994 Sep;7(3):233-41. doi: 10.1002/jmr.300070313.
We have studied the interaction of the A:T specific minor-groove binding ligand 4',6-diamidino-2-phenylindole (DAPI) with synthetic DNA oligomers containing specific binding sites in order to investigate possible long-range interactions between bound ligands. We find that DAPI binds cooperatively to the oligomers. The degree of cooperativity increases with increasing number of binding sites and decreases with the separation between them. This dependence is paralleled by changes in the induced circular dichroism spectrum of DAPI, which decreases in intensity at 335 nm and increases at 365 nm. These results are consistent with an allosteric interaction of DAPI with DNA, where bound ligands cooperatively alter the structure of the DNA molecule. This structural change seems possible to induce under various conditions, including physiological. One consequence of allosteric binding is that ligands bound at a distance from each other sense each other's presence and influence each others' properties. If some regulatory proteins induce the same conformational change as DAPI, novel mechanisms for controlling gene expression can be anticipated.
我们研究了A:T特异性小沟结合配体4',6-二脒基-2-苯基吲哚(DAPI)与含有特定结合位点的合成DNA寡聚物之间的相互作用,以研究结合配体之间可能存在的长程相互作用。我们发现DAPI与寡聚物协同结合。协同程度随着结合位点数量的增加而增加,随着它们之间距离的增加而降低。这种依赖性与DAPI诱导圆二色光谱的变化平行,在335nm处强度降低,在365nm处强度增加。这些结果与DAPI与DNA的变构相互作用一致,其中结合的配体协同改变DNA分子的结构。这种结构变化似乎在包括生理条件在内的各种条件下都有可能诱导发生。变构结合的一个结果是,彼此相距一定距离结合的配体能够感知彼此的存在并影响彼此的性质。如果某些调节蛋白诱导与DAPI相同的构象变化,那么可以预期会出现控制基因表达的新机制。