Albright R A, Matthews B W
Institute of Molecular Biology Howard Hughes Medical Institute and Department of Physics, University of Oregon, Eugene, OR, 97403-1229, USA.
J Mol Biol. 1998 Jul 3;280(1):137-51. doi: 10.1006/jmbi.1998.1848.
The structure of the Cro protein from bacteriophage lambda in complex with a 19 base-pair DNA duplex that includes the 17 base-pair consensus operator has been determined at 3.0 A resolution. The structure confirms the large changes in the protein and DNA seen previously in a crystallographically distinct low-resolution structure of the complex and, for the first time, reveals the detailed interactions between the side-chains of the protein and the base-pairs of the operator. Relative to the crystal structure of the free protein, the subunits of Cro rotate 53 degrees with respect to each other on binding DNA. At the same time the DNA is bent by 40 degrees through the 19 base-pairs. The intersubunit connection includes a region within the protein core that is structurally reminiscent of the "ball and socket" motif seen in the immunoglobulins and T-cell receptors. The crystal structure of the Cro complex is consistent with virtually all available biochemical and related data. Some of the interactions between Cro and DNA proposed on the basis of model-building are now seen to be correct, but many are different. Tests of the original model by mutagenesis and biochemical analysis corrected some but not all of the errors. Within the limitations of the crystallographic resolution it appears that operator recognition is achieved almost entirely by direct hydrogen-bonding and van der Waals contacts between the protein and the exposed bases within the major groove of the DNA. The discrimination of Cro between the operators OR3 and OR1, which differ in sequence at just three positions, is inferred to result from a combination of small differences, both favorable and unfavorable. A van der Waals contact at one of the positions is of primary importance, while the other two provide smaller, indirect effects. Direct hydrogen bonding is not utilized in this distinction.
噬菌体λ的Cro蛋白与包含17个碱基对共有操纵基因的19个碱基对DNA双链体形成复合物的结构已在3.0埃分辨率下确定。该结构证实了此前在复合物晶体学上不同的低分辨率结构中所观察到的蛋白质和DNA的巨大变化,并且首次揭示了蛋白质侧链与操纵基因碱基对之间的详细相互作用。相对于游离蛋白质的晶体结构,Cro的亚基在结合DNA时彼此相对旋转53度。与此同时,DNA通过19个碱基对弯曲了40度。亚基间连接包括蛋白质核心内的一个区域,其结构让人联想到在免疫球蛋白和T细胞受体中看到的“球窝”基序。Cro复合物的晶体结构与几乎所有现有的生化及相关数据一致。基于模型构建提出的Cro与DNA之间的一些相互作用现在看来是正确的,但许多是不同的。通过诱变和生化分析对原始模型进行的测试纠正了部分而非全部错误。在晶体学分辨率的限制范围内,似乎操纵基因识别几乎完全是通过蛋白质与DNA大沟内暴露碱基之间的直接氢键和范德华接触实现的。Cro对仅在三个位置序列不同的操纵基因OR3和OR1的区分,推断是由有利和不利的微小差异共同作用的结果。其中一个位置的范德华接触至关重要,而另外两个位置提供较小的间接影响。这种区分未利用直接氢键。