Galas D J, Schmitz A
Nucleic Acids Res. 1978 Sep;5(9):3157-70. doi: 10.1093/nar/5.9.3157.
A method for studying the sequence-specific binding of proteins to DBA is described. The technique is a simple conjoining of the Maxam-Gilbert DNA-sequencing method and the technique of DNAase-protected fragment isolation. Fragments of a 5' end-labelled, double-stranded DNA segment, partially degraded by DNAase in the presence and absence of the binding protein, are visualized by electrophoresis and autoradiography alongside the base-specific reaction products of the Maxam-Gilbert sequencing method. It is then possible to see the protective "footprint" of the binding protein on the DNA sequence. The binding of lac repressor to lac operator is visualized by "footprinting" as an example. Equillibrium estimates indicate that 10-fold sequence-specificity (differential binding constant) could be studied easily using this technique.
本文描述了一种研究蛋白质与脱氧核糖核酸(DNA)序列特异性结合的方法。该技术是将马克萨姆-吉尔伯特DNA测序方法与脱氧核糖核酸酶保护片段分离技术简单结合而成。在有和没有结合蛋白存在的情况下,用脱氧核糖核酸酶部分降解5′端标记的双链DNA片段,然后通过电泳和放射自显影将这些片段与马克萨姆-吉尔伯特测序方法的碱基特异性反应产物一起可视化。这样就可以看到结合蛋白在DNA序列上的保护性“足迹”。以“足迹”法显示了乳糖阻遏物与乳糖操纵基因的结合。平衡估计表明,使用该技术可以很容易地研究10倍的序列特异性(差异结合常数)。