Tsai S C, Adamik R, Manganiello V C, Vaughan M
Biochem J. 1983 Dec 1;215(3):447-55. doi: 10.1042/bj2150447.
Guanylate cyclase was purified from rat liver supernatant. Electrophoresis under denaturing conditions revealed one major peptide of Mr approx. 69 000. On the basis of the Stokes radius (4.7 nm) and S20,w (6.4S), the calculated Mr value of the native enzyme was 133 000, i.e. it is apparently a homodimer. Kinetics of inactivation by diamide (which was reversible with dithiothreitol) suggested that oxidation of a single class of thiol sites was involved. In the absence of other additions, cyclase activity assayed with Mn2+ was over 7 times that assayed with Mg2+; maximal effects were observed with approx. 5 mM of each (with 1 mM-GTP). The purified enzyme was markedly activated by nitrosylhaemoglobin. Relative activation was much greater in assays with Mg2+ than with Mn2+, although maximal activities were similar. When assayed with Mg2+, the enzyme exhibited a single Km (0.35 mM) for GTP; with Mn2+, plots of 1/v versus 1/[S] were non-linear. Activator or nitrosylhaemoglobin increased Vmax, but did not alter Km in the presence of either Mg2+ or Mn2+. The enzyme was inhibited by Na3VO4, Na2WO4 and Na2B4O7. Reduction from VV to VIV abolished the inhibitory effect of vanadate. Na2B4O7 (2 mM) inhibited activity with Mn2+, but not with Mg2+. In assays with Mg2+, but not with Mn2+, FMN, NAD+ and NADH (each 0.5 mM) inhibited activation by protoporphyrin IX and nitrosylhaemoglobin. Rotenone (0.6 mM) inhibited activity with protoporphyrin IX to a greater extent than with nitrosylhaemoglobin. Methylene Blue (1 mM) inhibited activation by nitrosylhaemoglobin, protoporphyrin IX and activator. It appears that this enzyme purified from rat liver lacks haem (and perhaps other components) required for activation by NO, and it should be particularly useful for elucidating the mechanism of action of NO, protoporphyrin IX and other activators.
鸟苷酸环化酶从大鼠肝脏上清液中纯化得到。变性条件下的电泳显示出一条主要肽段,其Mr约为69000。根据斯托克斯半径(4.7nm)和S20,w(6.4S),计算出天然酶的Mr值为133000,即它显然是一个同二聚体。二酰胺(可被二硫苏糖醇逆转)的失活动力学表明涉及一类单一的巯基位点的氧化。在没有其他添加物的情况下,用Mn2+测定的环化酶活性比用Mg2+测定的活性高7倍以上;在每种离子浓度约为5mM(同时含有1mM - GTP)时观察到最大效应。纯化的酶被亚硝基血红蛋白显著激活。在使用Mg2+的测定中相对激活程度比使用Mn2+时大得多,尽管最大活性相似。当用Mg2+测定时,该酶对GTP表现出单一的Km(0.35mM);用Mn2+时,1/v对1/[S]的作图呈非线性。激活剂或亚硝基血红蛋白增加Vmax,但在存在Mg2+或Mn2+时不改变Km。该酶被Na3VO4、Na2WO4和Na2B4O7抑制。从VV还原到VIV消除了钒酸盐的抑制作用。2mM的Na2B4O7抑制Mn2+存在时的活性,但不抑制Mg2+存在时的活性。在使用Mg2+而非Mn2+的测定中,FMN、NAD+和NADH(各0.5mM)抑制原卟啉IX和亚硝基血红蛋白的激活作用。鱼藤酮(0.6mM)对原卟啉IX存在时活性的抑制程度比对亚硝基血红蛋白存在时更大。亚甲蓝(1mM)抑制亚硝基血红蛋白、原卟啉IX和激活剂的激活作用。从大鼠肝脏纯化的这种酶似乎缺乏NO激活所需的血红素(可能还有其他成分),它对于阐明NO、原卟啉IX和其他激活剂的作用机制应该特别有用。