Winkler F K, Banner D W, Oefner C, Tsernoglou D, Brown R S, Heathman S P, Bryan R K, Martin P D, Petratos K, Wilson K S
Pharma Research-New Technologies, F. Hoffmann-La Roche Ltd, Basel, Switzerland.
EMBO J. 1993 May;12(5):1781-95. doi: 10.2210/pdb4rve/pdb.
The crystal structure of EcoRV endonuclease has been determined at 2.5 A resolution and that of its complexes with the cognate DNA decamer GGGATATCCC (recognition sequence underlined) and the non-cognate DNA octamer CGAGCTCG at 3.0 A resolution. Two octamer duplexes of the non-cognate DNA, stacked end-to-end, are bound to the dimeric enzyme in B-DNA-like conformations. The protein--DNA interactions of this complex are prototypic for non-specific DNA binding. In contrast, only one cognate decamer duplex is bound and deviates considerably from canonical B-form DNA. Most notably, a kink of approximately 50 degrees is observed at the central TA step with a concomitant compression of the major groove. Base-specific hydrogen bonds between the enzyme and the recognition base pairs occur exclusively in the major groove. These interactions appear highly co-operative as they are all made through one short surface loop comprising residues 182-186. Numerous contacts with the sugar phosphate backbone extending beyond the recognition sequence are observed in both types of complex. However, the total surface area buried on complex formation is > 1800 A2 larger in the case of cognate DNA binding. Two acidic side chains, Asp74 and Asp90, are close to the reactive phosphodiester group in the cognate complex and most probably provide oxygen ligands for binding the essential cofactor Mg2+. An important role is also indicated for Lys92, which together with the two acidic functions appears to be conserved in the otherwise unrelated structure of EcoRI endonuclease. The structural results give new insight into the physical basis of the remarkable sequence specificity of this enzyme.
EcoRV核酸内切酶的晶体结构已在2.5埃分辨率下测定,其与同源DNA十聚体GGGATATCCC(下划线为识别序列)和非同源DNA八聚体CGAGCTCG的复合物的晶体结构已在3.0埃分辨率下测定。两个首尾相连堆叠的非同源DNA八聚体双链体以类似B-DNA的构象与二聚体酶结合。这种复合物的蛋白质- DNA相互作用是非特异性DNA结合的典型例子。相比之下,只有一个同源十聚体双链体与之结合,且与典型的B型DNA有很大偏差。最值得注意的是,在中央TA步观察到约50度的扭结,同时大沟被压缩。酶与识别碱基对之间的碱基特异性氢键仅在大沟中形成。这些相互作用似乎具有高度协同性,因为它们都是通过一个包含182 - 186位残基的短表面环形成的。在两种类型的复合物中都观察到与延伸超出识别序列的糖磷酸骨架有大量接触。然而,在同源DNA结合的情况下,复合物形成时掩埋的总表面积要大> 1800 Ų。两个酸性侧链Asp74和Asp90在同源复合物中靠近反应性磷酸二酯基团,很可能为结合必需的辅因子Mg²⁺提供氧配体。Lys92也显示出重要作用,它与这两个酸性功能基团在EcoRI核酸内切酶其他不相关的结构中似乎是保守的。这些结构结果为该酶显著的序列特异性的物理基础提供了新的见解。