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A-form conformational motifs in ligand-bound DNA structures.

机译:配体结合的DNA结构中的A型构象基序。

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Recognition and biochemical processing of DNA requires that proteins and other ligands are able to distinguish their DNA binding sites from other parts of the molecule. In addition to the direct recognition elements embedded in the linear sequence of bases (i.e. hydrogen bonding sites), these molecular agents seemingly sense and/or induce an "indirect" conformational response in the DNA base-pairs that facilitates close intermolecular fitting. As part of an effort to decipher this sequence-dependent structural code, we have analyzed the extent of B-->A conformational conversion at individual base-pair steps in protein and drug-bound DNA crystal complexes. We take advantage of a novel structural parameter, the position of the phosphorus atom in the dimer reference frame, as well as other documented measures of local helical structure, e.g. torsion angles, base-pair step parameters. Our analysis pinpoints ligand-induced conformational changes that are difficult to detect from the global perspective used in other studies of DNA structure. The collective data provide new structural details on the conformational pathway connecting A and B-form DNA and illustrate how both proteins and drugs take advantage of the intrinsic conformational mechanics of the double helix. Significantly, the base-pair steps which exhibit pure A-DNA conformations in the crystal complexes follow the scale of A-forming tendencies exhibited by synthetic oligonucleotides in solution and the known polymorphism of synthetic DNA fibers. Moreover, most crystallographic examples of complete B-to-A deformations occur in complexes of DNA with enzymes that perform cutting or sealing operations at the (O3'-P) phosphodiester linkage. The B-->A transformation selectively exposes sugar-phosphate atoms, such as the 3'-oxygen atom, ordinarily buried within the chain backbone for enzymatic attack. The forced remodeling of DNA to the A-form also provides a mechanism for smoothly bending the double helix, for controlling the widths of the major and minor grooves, and for accessing the minor groove edges of individual base-pairs. Copyright 2000 Academic Press.
机译:DNA的识别和生化处理要求蛋白质和其他配体能够将其DNA结合位点与分子的其他部分区分开。除了嵌入线性碱基序列(即氢键结合位点)中的直接识别元件外,这些分子试剂似乎还感知和/或诱导DNA碱基对中的“间接”构象响应,这有助于紧密的分子间拟合。作为破译这种依赖序列的结构密码的努力的一部分,我们分析了蛋白质和药物结合的DNA晶体复合物中单个碱基对步骤中B-> A构象转化的程度。我们利用了新的结构参数,二聚体参考框架中磷原子的位置以及其他已记录的局部螺旋结构测量方法,例如扭转角,碱基对步长参数。我们的分析指出了配体诱导的构象变化,这些变化很难从其他DNA结构研究中使用的全局角度进行检测。收集的数据提供了有关连接A型和B型DNA的构象途径的新结构细节,并阐明了蛋白质和药物如何利用双螺旋的固有构象机制。重要的是,在晶体复合物中显示纯A-DNA构象的碱基对步骤遵循溶液中合成寡核苷酸表现出的A形成趋势的规模以及合成DNA纤维的已知多态性。此外,大多数B至A完全变形的晶体学实例都发生在DNA与在(O3'-P)磷酸二酯键处进行切割或封闭操作的酶的复合物中。 B→A转化选择性地暴露出糖-磷酸原子,例如3'-氧原子,该原子通常被埋在链骨架中以进行酶攻击。 DNA的强制重塑为A形还提供了一种机制,可以平滑地弯曲双螺旋,控制主凹槽和次凹槽的宽度,以及访问单个碱基对的次凹槽边缘。版权所有2000学术出版社。

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