Kameshita I, Matsuda Z, Taniguchi T, Shizuta Y
J Biol Chem. 1984 Apr 25;259(8):4770-6.
Poly(ADP-ribose) synthetase of Mr = 120,000 is cleaved by limited proteolysis with alpha-chymotrypsin into two fragments of Mr = 54,000 (54K) and Mr = 66,000 (66K). When the native enzyme is modified with 3-(bromoacetyl)pyridine, both portions of the enzyme are alkylated; however, alkylation of the 54K portions of the enzyme is protected by the addition of the substrate, NAD, or its analog, nicotinamide, suggesting that the substrate-binding site is localized in the 54K fragment. When the enzyme previously automodified with a low concentration of [adenine-U-14C] NAD is digested with alpha-chymotrypsin, the radioactivity is detected exclusively in the 66K fragment. The 66K fragment thus labeled is further cleaved with papain into two fragments of Mr = 46,000 and Mr = 22,000. With these two fragments, the label is detected only in the 22K fragment, but not in the 46K fragment. The 46K fragment binds to a DNA-cellulose column with the same affinity as that of the native enzyme, while the 22K fragment and the 54K fragment have little affinity for the DNA ligand. These results indicate that poly (ADP-ribose) synthetase contains three separable domains, the first possessing the site for binding of the substrate, NAD, the second containing the site for binding of DNA, and the third acting as the site(s) for accepting poly(ADP-ribose).
分子量为120,000的聚(ADP - 核糖)合成酶经α - 胰凝乳蛋白酶有限度的蛋白水解后,裂解成两个片段,分子量分别为54,000(54K)和66,000(66K)。当天然酶用3 - (溴乙酰基)吡啶修饰时,酶的两个部分均被烷基化;然而,酶的54K部分的烷基化可通过添加底物NAD或其类似物烟酰胺得到保护,这表明底物结合位点位于54K片段中。当先前用低浓度的[腺嘌呤 - U - 14C]NAD进行自身修饰的酶用α - 胰凝乳蛋白酶消化时,放射性仅在66K片段中检测到。如此标记的66K片段再用木瓜蛋白酶进一步裂解成分子量分别为46,000和22,000的两个片段。对于这两个片段,放射性仅在22K片段中检测到,而在46K片段中未检测到。46K片段与DNA - 纤维素柱结合的亲和力与天然酶相同,而22K片段和54K片段对DNA配体几乎没有亲和力。这些结果表明,聚(ADP - 核糖)合成酶包含三个可分离的结构域,第一个结构域具有底物NAD的结合位点,第二个结构域包含DNA的结合位点,第三个结构域作为接受聚(ADP - 核糖)的位点。