Straney D C, Straney S B, Crothers D M
Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, CT 06511.
J Mol Biol. 1989 Mar 5;206(1):41-57. doi: 10.1016/0022-2836(89)90522-6.
Characterization of ternary complexes containing an Escherichia coli lac promoter DNA fragment, CAP protein and RNA polymerase, separated on non-denaturing polyacrylamide gels and footprinted in the gel slice, reveals a striking stabilization of CAP against dissociation in the open complex, compared to the CAP-DNA complex lacking RNA polymerase. The stabilization is lost when half a helical turn of DNA is inserted between CAP and polymerase sites, but is partially restored with an 11 base-pair insert; stimulation of transcription parallels the stabilization effect. This behavior suggests a direct protein-protein interaction. Comparison of initiation kinetics for wild-type and a mutant in which the P2 promoter has been inactivated shows that CAP both strengthens binding in the closed complex and accelerates isomerization to the open complex; the latter effect accounts for the bulk of the observed transcriptional activation.
含有大肠杆菌乳糖启动子DNA片段、CAP蛋白和RNA聚合酶的三元复合物在非变性聚丙烯酰胺凝胶上分离,并在凝胶切片中进行足迹分析,结果显示,与缺乏RNA聚合酶的CAP-DNA复合物相比,在开放复合物中CAP抗解离的稳定性显著增强。当在CAP和聚合酶位点之间插入半个螺旋圈的DNA时,这种稳定性丧失,但插入11个碱基对时部分恢复;转录刺激与稳定作用平行。这种行为表明存在直接的蛋白质-蛋白质相互作用。对野生型和P2启动子已失活的突变体的起始动力学进行比较,结果表明,CAP既能增强在封闭复合物中的结合,又能加速向开放复合物的异构化;后一种效应是观察到的转录激活的主要原因。