Ash K, Berger T, Horner C M, Calvert C C
Department of Animal Science, University of California, Davis 95616-8521, USA.
Zygote. 1995 May;3(2):163-70. doi: 10.1017/s0967199400002537.
Sperm plasma membrane (PM) proteins that demonstrate affinity for egg PM preparations have the potential to be biologically important during sperm-egg binding and/or fusion. In this study four such proteins have been identified. To provide quantitative evidence for possible biological function, the large natural variation among different porcine sperm populations with regard to their ability to interact with the egg was compared with the relative binding of egg PM material to individual proteins. An aliquot from each of 24 porcine ejaculates was evaluated by the zona-free hamster ova bioassay and the remainder processed to yield sperm PM vesicles. Aliquots of sperm PM were solubilised, separated by SDS-PAGE, western blotted and probed with partially purified, biotinylated egg PM protein. Bound egg PM proteins were visualised on western blots by an avidin/biotin/horseradish peroxidase system and analysed by scanning laser densitometry. Four sperm PM proteins (62, 39, 27 and 7 kDa estimated molecular mass) were the predominant binders of egg PM. The amount of egg PM bound to the 62 kDa protein was significantly correlated with the ability of sperm from the 24 ejaculates to penetrate zona-free hamster ova (percentage of ova penetrated, p = 0.01, R = 0.65; number of penetrated sperm per ovum, p = 0.02, R = 0.63).
对卵细胞膜制剂具有亲和力的精子质膜(PM)蛋白,在精卵结合和/或融合过程中可能具有重要的生物学意义。在本研究中,已鉴定出四种此类蛋白。为了为可能的生物学功能提供定量证据,将不同猪精子群体在与卵相互作用能力方面的巨大天然差异,与卵细胞膜物质与单个蛋白的相对结合情况进行了比较。对24份猪精液中的每份精液取一份等分试样,通过无透明带仓鼠卵生物测定法进行评估,其余部分进行处理以产生精子质膜囊泡。将精子质膜的等分试样溶解,通过SDS-PAGE分离,进行蛋白质印迹,并用部分纯化的生物素化卵细胞膜蛋白进行检测。通过抗生物素蛋白/生物素/辣根过氧化物酶系统在蛋白质印迹上观察结合的卵细胞膜蛋白,并通过扫描激光密度测定法进行分析。四种精子质膜蛋白(估计分子量分别为62、39、27和7 kDa)是卵细胞膜的主要结合蛋白。与62 kDa蛋白结合的卵细胞膜量与24份精液中的精子穿透无透明带仓鼠卵的能力显著相关(卵穿透百分比,p = 0.01,R = 0.65;每个卵穿透的精子数,p = 0.02,R = 0.63)。