首页> 美国卫生研究院文献>Cell Regulation >Molecular Cloning and Characterization of a Radial Spoke Head Protein of Sea Urchin Sperm Axonemes: Involvement of the Protein in the Regulation of Sperm Motility
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Molecular Cloning and Characterization of a Radial Spoke Head Protein of Sea Urchin Sperm Axonemes: Involvement of the Protein in the Regulation of Sperm Motility

机译:海胆精子轴突径向辐头蛋白的分子克隆和表征:该蛋白参与精子运动的调节。

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摘要

Monoclonal antibodies raised against axonemal proteins of sea urchin spermatozoa have been used to study regulatory mechanisms involved in flagellar motility. Here, we report that one of these antibodies, monoclonal antibody D-316, has an unusual perturbating effect on the motility of sea urchin sperm models; it does not affect the beat frequency, the amplitude of beating or the percentage of motile sperm models, but instead promotes a marked transformation of the flagellar beating pattern which changes from a two-dimensional to a three-dimensional type of movement. On immunoblots of axonemal proteins separated by SDS-PAGE, D-316 recognized a single polypeptide of 90 kDa. This protein was purified following its extraction by exposure of axonemes to a brief heat treatment at 40°C. The protein copurified and coimmunoprecipitated with proteins of 43 and 34 kDa, suggesting that it exists as a complex in its native form. Using D-316 as a probe, a full-length cDNA clone encoding the 90-kDa protein was obtained from a sea urchin cDNA library. The sequence predicts a highly acidic (pI = 4.0) protein of 552 amino acids with a mass of 62,720 Da (p63). Comparison with protein sequences in databases indicated that the protein is related to radial spoke proteins 4 and 6 (RSP4 and RSP6) of Chlamydomonas reinhardtii, which share 37% and 25% similarity, respectively, with p63. However, the sea urchin protein possesses structural features distinct from RSP4 and RSP6, such as the presence of three major acidic stretches which contains 25, 17, and 12 aspartate and glutamate residues of 34-, 22-, and 14-amino acid long stretches, respectively, that are predicted to form α-helical coiled-coil secondary structures. These results suggest a major role for p63 in the maintenance of a planar form of sperm flagellar beating and provide new tools to study the function of radial spoke heads in more evolved species.
机译:针对海胆精子的轴突蛋白产生的单克隆抗体已用于研究与鞭毛运动有关的调节机制。在这里,我们报告说,其中一种抗体,单克隆抗体D-316,对海胆精子模型的运动性具有异常的干扰作用。它不会影响拍子的频率,跳动的幅度或运动精子模型的百分比,而会促进鞭毛跳动模式的明显转变,这种运动会从二维运动方式转变为三维运动方式。在通过SDS-PAGE分离的轴索蛋白免疫印迹上,D-316识别出一个90 kDa的多肽。该蛋白在提取后,通过将轴酮暴露于40°C的简短热处理中进行纯化。该蛋白与43和34 kDa的蛋白共纯化和共免疫沉淀,表明它以其天然形式作为复合物存在。使用D-316作为探针,从海胆cDNA文库中获得了编码90 kDa蛋白的全长cDNA克隆。该序列预测了552个氨基酸的高酸性(pI = 4.0)蛋白,质量为62,720 Da(p63)。与数据库中蛋白质序列的比较表明,该蛋白质与莱茵衣藻的径向辐状蛋白质4和6(RSP4和RSP6)有关,它们与p63分别具有37%和25%的相似性。但是,海胆蛋白具有不同于RSP4和RSP6的结构特征,例如存在三个主要的酸性链段,其中包含25、17和12个天冬氨酸和谷氨酸残基,分别具有34、22和14个氨基酸长链段分别被预测形成α-螺旋盘绕二级结构。这些结果表明p63在维持精子鞭毛跳动的平面形式中起主要作用,并提供了新的工具来研究更多进化物种中的放射状辐照头的功能。

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