Olson G E, Lifsics M R, Winfrey V P, Rifkin J M
J Androl. 1987 May-Jun;8(3):129-47. doi: 10.1002/j.1939-4640.1987.tb02424.x.
Previously, we demonstrated that surface radiolabeling of rat epididymal spermatozoa by lactoperoxidase-catalyzed iodination reveals a major component with an apparent molecular weight of 26,000 to 28,000 daltons (26 kDa) on spermatozoa from the cauda but not the caput epididymidis. To characterize this surface component further, sperm surface constituents radiolabeled by lactoperoxidase-catalyzed iodination were separated by 2-D PAGE. The 26 kDa component was localized by autoradiography and appeared as the major labeled acidic spot on cauda spermatozoa, but neither a radiolabeled spot nor a corresponding stained spot was present on caput spermatozoa. The 26 kDa spot was excised from 2-D gels of plasma membranes from cauda spermatozoa and utilized for immunization. The monospecific antiserum stained a single band of 26 kDa on Western blots of SDS-PAGE-separated plasma membranes from cauda spermatozoa and in a 100,000 X g supernatant fluid of the luminal contents of the cauda epididymidis. Immunohistochemical staining of cauda spermatozoa revealed antigen exclusively on the flagellar domain; the antigen was not seen on caput spermatozoa but first appeared in spermatozoa from the proximal corpus epididymidis. Immunoelectron microscopy confirmed the 26 kDa component was localized to the external face of the flagellar plasma membrane. Immunohistochemical staining of caput spermatozoa incubated in vitro with cauda epididymal luminal fluid revealed the 26 kDa component specifically bound the flagellar domain of immature spermatozoa.
此前,我们证明,通过乳过氧化物酶催化碘化对大鼠附睾精子进行表面放射性标记,显示来自附睾尾部而非头部的精子上有一个主要成分,其表观分子量为26,000至28,000道尔顿(26 kDa)。为了进一步表征这种表面成分,通过二维聚丙烯酰胺凝胶电泳(2-D PAGE)分离经乳过氧化物酶催化碘化放射性标记的精子表面成分。通过放射自显影定位26 kDa成分,其在附睾尾部精子上表现为主要的标记酸性斑点,但在附睾头部精子上既没有放射性标记斑点也没有相应的染色斑点。从附睾尾部精子的质膜二维凝胶中切下26 kDa斑点并用于免疫。单特异性抗血清在来自附睾尾部精子的十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)分离的质膜的蛋白质免疫印迹上以及在附睾尾部管腔内容物的100,000×g上清液中染出一条26 kDa的单带。附睾尾部精子的免疫组织化学染色显示抗原仅存在于鞭毛区域;在附睾头部精子上未见到该抗原,但其首次出现在附睾近端体部的精子中。免疫电子显微镜证实26 kDa成分定位于鞭毛质膜的外表面。用附睾尾部管腔液体外孵育的附睾头部精子的免疫组织化学染色显示,26 kDa成分特异性结合未成熟精子的鞭毛区域。