Wharton R P, Ptashne M
Nature. 1985;316(6029):601-5. doi: 10.1038/316601a0.
We replaced amino acids on the 'outside', or solvent-exposed, surface of the DNA recognition alpha-helix of 434 repressor with the corresponding amino acids from the recognition helix of P22 repressor. The binding specificity of the resulting hybrid protein, as measured in vivo and in vitro, was that of P22 repressor.
我们用P22阻遏蛋白识别螺旋中的相应氨基酸取代了434阻遏蛋白DNA识别α螺旋“外部”或溶剂暴露表面上的氨基酸。在体内和体外测量时,所得杂交蛋白的结合特异性是P22阻遏蛋白的结合特异性。