Roth A, Messer W
Max-Planck-Institut für Molekulare Genetik, Berlin-Dahlem, Germany.
EMBO J. 1995 May 1;14(9):2106-11. doi: 10.1002/j.1460-2075.1995.tb07202.x.
The 94 C-terminal amino acids of the initiator protein DnaA of Escherichia coli are required and sufficient for specific binding to the cognate DNA binding site. The binding domain contains two potential amphipathic alpha-helices and a third alpha-helix. It represents a new DNA binding motif so far not found in other DNA binding proteins. Temperature-sensitive mutations in the binding motif, dnaA204, dnaA205 and dnaA211, abolish DNA binding. In the solid-phase DNA binding assay, applicable to other DNA binding proteins, fusions of domains of DnaA protein to beta-galactosidase are reacted with biotinylated anti-beta-galactosidase antibody. These are coupled to streptavidin-coated magnetic beads. The DNA binding domain is able to selectively remove the DNA target (oriC) from the liquid phase. Alternatively, the DNA binding domain is fused to a peptide containing a target sequence which is naturally biotinylated in vivo in E.coli. This fusion protein can be coupled directly to streptavidin-coated magnetic beads. Homologies between DnaA protein and transcription factors of the NtrC family are discussed.
大肠杆菌起始蛋白DnaA的94个C末端氨基酸对于与同源DNA结合位点的特异性结合是必需且充分的。该结合结构域包含两个潜在的两亲性α螺旋和第三个α螺旋。它代表了一种迄今为止在其他DNA结合蛋白中未发现的新的DNA结合基序。结合基序中的温度敏感突变dnaA204、dnaA205和dnaA211会消除DNA结合。在适用于其他DNA结合蛋白的固相DNA结合试验中,DnaA蛋白结构域与β-半乳糖苷酶的融合物与生物素化的抗β-半乳糖苷酶抗体反应。这些抗体与链霉亲和素包被的磁珠偶联。DNA结合结构域能够从液相中选择性地去除DNA靶标(oriC)。或者,将DNA结合结构域与含有靶序列的肽融合,该靶序列在大肠杆菌体内天然被生物素化。这种融合蛋白可以直接与链霉亲和素包被的磁珠偶联。文中还讨论了DnaA蛋白与NtrC家族转录因子之间的同源性。