Peterson R N, Hunt W P
Department of Physiology, School of Medicine, Southern Illinois University, Carbondale 62901-6512.
Gamete Res. 1989 May;23(1):103-18. doi: 10.1002/mrd.1120230110.
Boar sperm plasma membranes contain an integral protein (Mr 55 kDa) that apparently functions in the adhesion of sperm to the zona pellucida (Peterson and Hunt: J Cell Biol 105:170a, 1987.) In experiments described in this report, the protein is identified after additional steps of purification involving lectin affinity chromatography and preparative PAGE. An active form of the adhesion protein (APz) develops or becomes first exposed in the corpus epididymis and is fully active in the cauda epididymis; a significant portion of this conformationally labile protein, while integral to the plasma membrane, cannot be solubilized by nonionic detergents and may be associated with the membrane skeleton. APz does not exhibit enzymatic properties thought possibly to be involved in sperm-zona interaction in this and other species. Galactosyltransferase substrates and inhibitors and antiproteases including soybean trypsin inhibitor, pepstatin, leupeptin, and p-aminobenzamidine failed to block sperm from binding to porcine eggs. Boar sperm proacrosin and antiproacrosin antibody failed to inhibit sperm-egg binding. When plasma membranes or fractions containing APz that bind to dextran sulfate agarose were chromatographed on L-fucose agarose, a sugar which binds proacrosin, plasma membrane proteins that bound to the column failed to absorb anti-APz antibody. Anti-APz was absorbed by fractions that did not contain proacrosin. These data indicate that APz is not proacrosin. Since anti-APz monovalent antibody raised from whole cauda or corpus sperm plasma membranes or from chromatographic fractions containing APz completely block capacitated sperm from binding to eggs, and since the ability of this antibody to be absorbed develops as sperm become capable of binding to eggs, we view APz to be the major and perhaps only plasma membrane protein involved in the adhesion of capacitated boar sperm to eggs prior to the acrosome reaction.
公猪精子质膜含有一种整合蛋白(分子量55 kDa),该蛋白显然在精子与透明带的黏附中发挥作用(彼得森和亨特:《细胞生物学杂志》105:170a,1987年)。在本报告所述的实验中,经过涉及凝集素亲和层析和制备性聚丙烯酰胺凝胶电泳的额外纯化步骤后鉴定出了该蛋白。黏附蛋白(APz)的活性形式在附睾体中形成或首次暴露,并在附睾尾中完全具有活性;这种构象不稳定的蛋白的很大一部分虽然是质膜的组成部分,但不能被非离子去污剂溶解,可能与膜骨架相关。APz不具有可能参与该物种及其他物种精子与透明带相互作用的酶活性。半乳糖基转移酶底物、抑制剂以及抗蛋白酶(包括大豆胰蛋白酶抑制剂、胃蛋白酶抑制剂、亮抑酶肽和对氨基苯甲脒)均未能阻止精子与猪卵结合。公猪精子前顶体蛋白酶和抗前顶体蛋白酶抗体未能抑制精子与卵子的结合。当与硫酸葡聚糖琼脂糖结合的质膜或含有APz的组分在L-岩藻糖琼脂糖(一种与前顶体蛋白酶结合的糖)上进行层析时,与柱结合的质膜蛋白未能吸附抗APz抗体。抗APz被不含前顶体蛋白酶的组分吸附。这些数据表明APz不是前顶体蛋白酶。由于从整个附睾尾或附睾体精子质膜或含有APz的层析组分中产生的抗APz单价抗体完全阻止获能精子与卵子结合,并且由于这种抗体被吸附的能力随着精子能够与卵子结合而发展,我们认为APz是在顶体反应之前参与获能公猪精子与卵子黏附的主要且可能是唯一的质膜蛋白。