Simonin F, Ménissier-de Murcia J, Poch O, Muller S, Gradwohl G, Molinete M, Penning C, Keith G, de Murcia G
Institut de Biologie Moléculaire et cellulaire du Centre National de la Recherche Scientifique, Laboratoires de Biochimie, Strasbourg, France.
J Biol Chem. 1990 Nov 5;265(31):19249-56.
Bacterially expressed fusion proteins containing the COOH-terminal domain of the human poly(ADP-ribose)polymerase were analyzed by means of a novel assay, the "activity blot," which allows the detection of transferred polypeptides involved in poly(ADP-ribose) synthesis. Deletion analysis demonstrated that the 40-kDa COOH-terminal region of the enzyme is an autonomous catalytic domain exhibiting both the polymerizing and branching activities in the absence of DNA. Site-directed mutagenesis demonstrated that lysine 893 is essential for these catalytic processes. In addition, sequence similarities obtained with the NAD(P)+ amino acid dehydrogenases suggest that (i) lysine 893 may interact with the substrates of poly(ADP-ribose)polymerase and (ii) the COOH-terminal part of the 40-kDa fragment may also contain a Rossman fold structure.
通过一种新型检测方法“活性印迹法”,对含有人类聚(ADP - 核糖)聚合酶羧基末端结构域的细菌表达融合蛋白进行了分析,该方法能够检测参与聚(ADP - 核糖)合成的转移多肽。缺失分析表明,该酶40 kDa的羧基末端区域是一个自主催化结构域,在无DNA的情况下表现出聚合和分支活性。定点诱变表明,赖氨酸893对这些催化过程至关重要。此外,与NAD(P)+氨基酸脱氢酶的序列相似性表明:(i)赖氨酸893可能与聚(ADP - 核糖)聚合酶的底物相互作用;(ii)40 kDa片段的羧基末端部分可能还包含一个罗斯曼折叠结构。