Fujinoki Masakatsu, Kawamura Takeshi, Toda Toshifusa, Ohtake Hideki, Shimizu Nobuyoshi, Yamaoka Sadao, Okuno Makoto
Department of Physiology, Dokkyo University School of Medicine, Mibu, Tochigi 321-0293.
J Biochem. 2003 Oct;134(4):559-65. doi: 10.1093/jb/mvg174.
In our previous paper [M. Fujinoki et al. (2001) BIOMED: Res. 22, 45-58], we reported that the 58-kDa protein obtained from hamster sperm flagella was phosphorylated at serine residues in association with the start of motility. In the present experiments, we identified and localized the 58-kDa protein. The 58-kDa protein was assumed to exist in the acrosomal region domain of the sperm head and the whole sperm flagellum. In particular, a large amount of 58-kDa protein was localized in the equatorial segment of the acrosomal region domain of the sperm head and the middle piece of the sperm flagellum. In the next step, the 58-kDa protein was identified by peptide mass finger printing and LC-MS/MS analysis. The results suggested that the 58-kDa protein was ATP synthase H(+) transporting F1 beta, which is one of the mitochondrial components. Therefore, it is likely that the 58-kDa protein is associated with ATP production in the mitochondrial sheath in the middle piece of the sperm flagellum, and H(+) transport in the sperm head and the sperm flagellum except for the middle piece, since ATP synthase also acts as an H(+) pump.
在我们之前的论文[藤木真等人(2001年),《生物医学研究》22卷,第45 - 58页]中,我们报道了从仓鼠精子鞭毛中获得的58 kDa蛋白在丝氨酸残基处发生磷酸化,且与精子运动的开始相关。在本实验中,我们对该58 kDa蛋白进行了鉴定和定位。推测该58 kDa蛋白存在于精子头部的顶体区域以及整个精子鞭毛中。特别地,大量的58 kDa蛋白定位于精子头部顶体区域的赤道段以及精子鞭毛的中段。下一步,通过肽质量指纹图谱和液相色谱 - 串联质谱分析对58 kDa蛋白进行了鉴定。结果表明,该58 kDa蛋白是ATP合酶H(+)转运F1β,它是线粒体的组成成分之一。因此,58 kDa蛋白很可能与精子鞭毛中段线粒体鞘中的ATP产生以及精子头部和除中段外的精子鞭毛中的H(+)转运相关,因为ATP合酶也起到H(+)泵的作用。