Stormo G D, Strobl S, Yoshioka M, Lee J S
Department of Molecular, Cellular and Developmental Biology, University of Colorado, Boulder 80309-0347.
J Mol Biol. 1993 Feb 20;229(4):821-6. doi: 10.1006/jmbi.1993.1088.
The relative binding affinities of Mnt protein are determined for each possible base-pair at position 15 of the operator sequence, and for all combinations of G.C base-pairs at positions 15 and 17. The partitioning of each operator sequence is determined quantitatively with restriction enzymes. At position 15, the wild-type G.C base-pair provides the highest binding affinity but, unlike position 17, the primary distinction is between purine and pyrimidine bases on the top strand. The information content at position 15 is only about 0.16 bit. In comparison with previous measurements at position 17, it is determined that the interactions of the Mnt protein with positions 15 and 17 are independent, i.e. the specific binding energies for the two positions are additive. The relative binding affinities at position 17 are also determined in the background of a G to T mutation at position 5, the position equivalent to 17 on the other half of the symmetric operator. The relative affinities at position 17 are independent of whether position 5 is wild-type or mutant.
测定了Mnt蛋白与操纵序列第15位每个可能碱基对以及第15位和第17位G.C碱基对所有组合的相对结合亲和力。用限制性内切酶定量确定每个操纵序列的分配情况。在第15位,野生型G.C碱基对提供最高的结合亲和力,但与第17位不同的是,主要区别在于上链上的嘌呤和嘧啶碱基之间。第15位的信息含量仅约0.16比特。与之前在第17位的测量结果相比,确定Mnt蛋白与第15位和第17位的相互作用是独立的,即两个位置的特异性结合能是相加的。在对称操纵子另一半相当于第17位的第5位发生G到T突变的背景下,也测定了第17位的相对结合亲和力。第17位的相对亲和力与第5位是野生型还是突变型无关。