Buckle M, Geiselmann J, Kolb A, Buc H
Institut Pasteur, Unité de Physicochimie des Macromolécules Biologiques (URA 1149 du CNRS), Paris, France.
Nucleic Acids Res. 1991 Feb 25;19(4):833-40. doi: 10.1093/nar/19.4.833.
We report the results of photo-cross-linking of RNA polymerase and the cyclic AMP receptor protein (CRP) to the lac UV5 promoter region carried on either a linear fragment or a supercoiled plasmid. We have devised a protocol that allows the localisation of bases in contact with the protein. RNA polymerase makes contacts within the -10 and -35 regions of the promoter, essentially on the non-template strand. The CRP contact points found in a binary complex are affected by the formation of the ternary complex containing RNA polymerase. Supercoiling has no effect on the position of contacts in any of the complexes. These conclusions were derived from experiments performed using a generally applicable, non-interfering technique that reveals direct contacts between proteins and nucleic acids in nucleoprotein complexes.
我们报告了RNA聚合酶和环磷酸腺苷受体蛋白(CRP)与线性片段或超螺旋质粒上携带的lac UV5启动子区域进行光交联的结果。我们设计了一种方案,可对与蛋白质接触的碱基进行定位。RNA聚合酶在启动子的-10和-35区域内形成接触,基本上是在非模板链上。在二元复合物中发现的CRP接触点会受到包含RNA聚合酶的三元复合物形成的影响。超螺旋对任何复合物中接触位点的位置均无影响。这些结论来自使用一种普遍适用、无干扰技术进行的实验,该技术揭示了核蛋白复合物中蛋白质与核酸之间的直接接触。