Rau D C, Gellert M, Thoma F, Maxwell A
J Mol Biol. 1987 Feb 5;193(3):555-69. doi: 10.1016/0022-2836(87)90266-x.
We have analyzed the structure of complexes between DNA gyrase and four defined DNA fragments by electric dichroism. Both the extrapolated dichroism and relaxation time of these complexes suggest that a single turn of DNA is wrapped around the enzyme with the entry and exit points located close together. The average angle between the DNA tails emerging from the particle is about 120 degrees. This structure is consistent with that seen by electron microscopy. Addition of ATP or the non-hydrolyzable ATP analog 5'-adenylyl-beta, gamma-imidodiphosphate results in a structural change of the complex, consistent with the DNA tails now being wrapped around the protein. The significance of these observations with respect to the mechanism of DNA supercoiling by DNA gyrase is discussed.
我们通过电二色性分析了DNA促旋酶与四个特定DNA片段之间复合物的结构。这些复合物的外推二色性和弛豫时间均表明,DNA单链环绕酶,其进入和退出点靠得很近。从颗粒中伸出的DNA尾部之间的平均角度约为120度。这种结构与电子显微镜观察到的结构一致。添加ATP或不可水解的ATP类似物5'-腺苷-β,γ-亚氨二磷酸会导致复合物的结构发生变化,这与现在DNA尾部环绕蛋白质的情况一致。讨论了这些观察结果对于DNA促旋酶进行DNA超螺旋化机制的意义。