Kopf G S, Woolkalis M J, Gerton G L
J Biol Chem. 1986 Jun 5;261(16):7327-31.
The abalone sperm adenylate cyclase does not appear to be regulated by guanine nucleotides, but has a Mg2+-supported catalytic activity similar to other hormone- and guanine nucleotide-regulated enzymes (Kopf, G. S., and Vacquier, V. D. (1984) J. Biol. Chem. 259, 7590-7596; Kopf, G. S., and Vacquier, V. D. (1985) Biol. Reprod. 33, 1094-1104). The present studies were undertaken to ascertain whether the abalone enzyme has associated guanine nucleotide-binding regulatory proteins. Membrane fractions were incubated with either islet-activating protein (IAP) or cholera toxin and analyzed by sodium dodecyl sulfate SDS-polyacrylamide gel electrophoresis for the presence of toxin-catalyzed ADP-ribosylated proteins. The supernatant from a Lubrol PX-extracted 48,000 X g pellet fraction contained a Mr = 41,000 IAP substrate. This substrate could not be ADP-ribosylated prior to detergent extraction. Lubrol PX-solubilized fractions of membrane preparations from mouse, bovine, and human sperm also contained a Mr = 41,000 IAP substrate. These proteins co-migrated on sodium dodecyl sulfate-polyacrylamide gels with the Mr = 41,000 alpha i-subunit of the inhibitory guanine nucleotide-binding regulatory protein (Gi) from transformed chicken embryo fibroblast and mouse S-49 lymphoma membrane extracts. The sperm IAP substrates displayed similar protease digest patterns to alpha i of mouse S-49 lymphoma cells. Sea urchin sperm analyzed in a similar manner contained a Mr = 39,000 IAP substrate. Cholera toxin-catalyzed ADP-ribosylation of specific sperm membrane proteins was not observed in any of the sperm preparations tested. The presence of the beta-subunit common to both the stimulatory and inhibitory guanine nucleotide-binding regulatory heterotrimers was confirmed in sperm using an antiserum directed against the purified beta-subunit of the guanine nucleotide-binding regulatory proteins from bovine brain. It is concluded that all of the sperm tested, with the possible exception of sea urchin sperm, contain a Gi-like protein. Additional properties of these proteins and their role(s) in sperm function are currently being examined.
鲍鱼精子腺苷酸环化酶似乎不受鸟嘌呤核苷酸的调节,但具有类似于其他受激素和鸟嘌呤核苷酸调节的酶的Mg2 +支持的催化活性(科夫,G.S.,和瓦奎尔,V.D.(1984)《生物化学杂志》259,7590 - 7596;科夫,G.S.,和瓦奎尔,V.D.(1985)《生殖生物学》33,1094 - 1104)。进行本研究以确定鲍鱼酶是否具有相关的鸟嘌呤核苷酸结合调节蛋白。将膜组分与胰岛激活蛋白(IAP)或霍乱毒素一起孵育,并通过十二烷基硫酸钠 - SDS - 聚丙烯酰胺凝胶电泳分析毒素催化的ADP - 核糖基化蛋白的存在情况。来自Lubrol PX提取的48,000×g沉淀组分的上清液含有一种Mr = 41,000的IAP底物。在去污剂提取之前,该底物不能被ADP - 核糖基化。来自小鼠、牛和人类精子的膜制剂的Lubrol PX增溶组分也含有一种Mr = 41,000的IAP底物。这些蛋白质在十二烷基硫酸钠 - 聚丙烯酰胺凝胶上与来自转化鸡胚成纤维细胞和小鼠S - 49淋巴瘤膜提取物的抑制性鸟嘌呤核苷酸结合调节蛋白(Gi)的Mr = 41,000αi亚基共迁移。精子IAP底物显示出与小鼠S - 49淋巴瘤细胞的αi相似的蛋白酶消化模式。以类似方式分析的海胆精子含有一种Mr = 39,000的IAP底物。在任何测试的精子制剂中均未观察到霍乱毒素催化的特定精子膜蛋白的ADP - 核糖基化。使用针对来自牛脑的鸟嘌呤核苷酸结合调节蛋白的纯化β亚基的抗血清,在精子中证实了刺激性和抑制性鸟嘌呤核苷酸结合调节异源三聚体共有的β亚基的存在。得出的结论是,除海胆精子可能例外,所有测试的精子都含有一种类似Gi的蛋白。目前正在研究这些蛋白质的其他特性及其在精子功能中的作用。