Stormo G D, Yoshioka M
Department of Molecular, Cellular and Developmental Biology, University of Colorado, Boulder 80309-0347.
Proc Natl Acad Sci U S A. 1991 Jul 1;88(13):5699-703. doi: 10.1073/pnas.88.13.5699.
The relative binding affinities of Mnt protein from bacteriophage P22 are determined for each possible base pair at position 17 of the operator. These are determined from the partitioning of randomized operators into bound and unbound fractions; quantitation is provided by restriction enzyme analysis. Mnt protein is found to have an unusual specificity at this position: a C.G base pair (the wild-type operator) has the highest affinity, a G.C base pair has the lowest affinity, and both orientations of A.T base pairs are intermediate and nearly equivalent. A specific binding constant and specific binding free energy are defined and shown to be directly related to the information content of the operator sequences bound to the protein, taking into account the quantitative differences in binding affinities.
测定了来自噬菌体P22的Mnt蛋白对操纵基因第17位每个可能碱基对的相对结合亲和力。这些亲和力是通过将随机化的操纵基因分为结合部分和未结合部分来确定的;通过限制酶分析进行定量。发现Mnt蛋白在该位置具有不同寻常的特异性:C.G碱基对(野生型操纵基因)具有最高亲和力,G.C碱基对具有最低亲和力,A.T碱基对的两种方向亲和力处于中间且几乎相等。定义了一个特异性结合常数和特异性结合自由能,并表明它们与结合到该蛋白的操纵基因序列的信息含量直接相关,同时考虑到结合亲和力的定量差异。