Zeheb R, Orr G A
J Biol Chem. 1984 Jan 25;259(2):839-48.
A Mr = 32,000 membrane glycoprotein can be uniquely labeled by galactose oxidase/[3H]sodium borohydride on rat caudal, but not caput, epididymal sperm. It has been suggested that this protein is related to a Mr = 32,000 galactose oxidase-sensitive glycoprotein present in rat caudal epididymal fluid. The tritiated membrane glycoprotein was solubilized and its hydrodynamic properties were determined by conventional gel filtration, high performance gel filtration, sedimentation rate determination in linear sucrose gradients prepared in H2O and D2O, and equilibrium isopycnic centrifugations in CsCl. The Stokes radius and sedimentation coefficient were 4.87 +/- 0.07 nm and 1.73 +/- 0.08 S, respectively. The sedimentation profile in CsCl gradients was asymmetric with a major peak occurring at a density of 1.081 g/cm3 (v = 0.92 cm3/g) and a shoulder at 1.108 g/cm3 (v = 0.90 cm3/g). The glycoprotein did not enter a 5 to 20% linear sucrose gradient prepared in D2O and could be extracted from the intact sperm into acidic chloroform:methanol solutions. These data are consistent with a protein which binds substantial amounts of detergent and/or lipid and has exposed hydrophobic regions. Two-dimensional gel electrophoresis indicated that the membrane protein exhibits charge heterogeneity, with the major components having pI values of 5.4 and 4.9. The fluid glycoprotein was monodisperse on two-dimensional gel electrophoresis having a pI of 3.8. Binding studies failed to demonstrate specific binding of the Mr = 32,000 caudal fluid glycoprotein to caput cells. Moreover, "Western blots" of electrophoretically resolved caput and caudal fluid proteins, followed by immunolabeling with antibodies raised against unfractionated caudal fluid, demonstrated the presence of a Mr = 32,000 protein in caudal fluid which was absent from caput epididymal fluid. Using the same technique, it was shown that antibodies raised against caudal fluid proteins did not cross-react with a Mr = 32,000 caudal membrane glycoprotein. Our data do not support the view that the Mr = 32,000 fluid and membrane proteins are identical.
一种分子量为32,000的膜糖蛋白可被半乳糖氧化酶/[³H]硼氢化钠特异性标记于大鼠尾部附睾精子,但不能标记头部附睾精子。有人提出,这种蛋白质与大鼠尾部附睾液中存在的一种分子量为32,000的半乳糖氧化酶敏感糖蛋白有关。将标记有³H的膜糖蛋白溶解,并通过常规凝胶过滤、高效凝胶过滤、在H₂O和D₂O中制备的线性蔗糖梯度中测定沉降速率以及在CsCl中进行平衡等密度离心来确定其流体动力学性质。斯托克斯半径和沉降系数分别为4.87±0.07纳米和1.73±0.08 S。在CsCl梯度中的沉降曲线不对称,主要峰出现在密度为1.081克/立方厘米(v = 0.92立方厘米/克)处,在1.108克/立方厘米(v = 0.90立方厘米/克)处有一个肩峰。该糖蛋白不进入在D₂O中制备的5%至20%线性蔗糖梯度,并且可以从完整精子中提取到酸性氯仿:甲醇溶液中。这些数据与一种结合大量去污剂和/或脂质且具有暴露疏水区域的蛋白质一致。二维凝胶电泳表明,膜蛋白表现出电荷异质性,主要成分的等电点值为5.4和4.9。流体糖蛋白在等电点为3.8的二维凝胶电泳上是单分散的。结合研究未能证明分子量为32,000的尾部液糖蛋白与头部细胞的特异性结合。此外,对头部和尾部液蛋白进行电泳分离后进行“免疫印迹”,然后用针对未分级尾部液产生的抗体进行免疫标记,结果表明尾部液中存在一种分子量为32,000的蛋白,而头部附睾液中不存在。使用相同技术表明,针对尾部液蛋白产生的抗体与分子量为32,000的尾部膜糖蛋白不发生交叉反应。我们的数据不支持分子量为32,000的液蛋白和膜蛋白相同的观点。