Broyde Suse, Wang Lihua, Zhang Ling, Rechkoblit Olga, Geacintov Nicholas E, Patel Dinshaw J
Department of Biology, New York University, New York NY 10003, USA.
Chem Res Toxicol. 2008 Jan;21(1):45-52. doi: 10.1021/tx700193x. Epub 2007 Dec 4.
It has now been nearly two decades since the first solution structures of DNA duplexes covalently damaged by metabolically activated polycyclic aromatic hydrocarbons and amines were determined by NMR. Dozens of such high-resolution structures are now available, and some broad structural themes have been uncovered. It has been hypothesized that the solution structures are relevant to the biochemical processing of the adducts. The structural features of the adducts are considered to determine their mutational properties in DNA polymerases and their repair susceptibilities. In recent years, a number of crystal structures of DNA adducts of interest to our work have been determined in DNA polymerases. Accordingly, it is now timely to consider how NMR solution structures relate to structures within DNA polymerases. The NMR solution structural themes for polycyclic aromatic adducts are often observed in polymerase crystal structures. While the polymerase interactions can on occasion override the solution preferences, intrinsic adduct conformations favored in solution are often manifested within polymerases and likely play a significant role in lesion processing.
自通过核磁共振确定了由代谢活化的多环芳烃和胺共价损伤的DNA双链体的首批溶液结构以来,至今已近二十年。现在已有数十种此类高分辨率结构,并且发现了一些广泛的结构主题。据推测,溶液结构与加合物的生化处理相关。加合物的结构特征被认为决定了它们在DNA聚合酶中的突变特性及其修复敏感性。近年来,已确定了一些与我们工作相关的DNA加合物在DNA聚合酶中的晶体结构。因此,现在是时候考虑核磁共振溶液结构与DNA聚合酶内的结构有何关联了。多环芳烃加合物的核磁共振溶液结构主题在聚合酶晶体结构中经常可见。虽然聚合酶的相互作用有时会压倒溶液中的偏好,但溶液中 favored的内在加合物构象通常会在聚合酶中表现出来,并可能在损伤处理中发挥重要作用。 (注:原文中“favored”前面似乎少了些内容,翻译时保留了原文的不完整性)