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顶体完整的小鼠精子上透明带糖蛋白3(ZP3)和ZP2结合位点的特征

Characterization of zona pellucida glycoprotein 3 (ZP3) and ZP2 binding sites on acrosome-intact mouse sperm.

作者信息

Kerr Candace L, Hanna William F, Shaper Joel H, Wright William W

机构信息

Division of Reproductive Biology, Department of Biochemistry and Molecular Biology, The Johns Hopkins University Bloomberg School of Public Health, Baltimore, Maryland 21205-2179, USA.

出版信息

Biol Reprod. 2002 Jun;66(6):1585-95. doi: 10.1095/biolreprod66.6.1585.

Abstract

There is considerable evidence that mouse fertilization requires the binding of sperm to two of the three glycoproteins that form the zona pellucida (ZP), ZP3 and ZP2. Despite the biologic importance of this binding, no one has demonstrated that sperm express separate, saturable, and specific binding sites for ZP3 and for ZP2. Such a demonstration is a prerequisite for defining the distribution, numbers, affinities, and regulation of function of ZP3 and ZP2 binding sites on sperm. The experiments reported herein used fluorochrome-labeled ZP3 and ZP2 and quantitative image analysis to characterize the saturable binding of ZP3 and ZP2 to distinct sites on living, capacitated, acrosome-intact mouse sperm. Approximately 20% of the ZP3 binding sites were found over the acrosomal cap, and the remaining sites were located over the postacrosomal region of the head. In contrast, ZP2 binding sites were detected only over the postacrosomal region. Saturation analysis estimated numbers and affinities of the binding sites for ZP3 (B(max) approximately 185 000 sites per sperm; K(d) approximately 67 nM) and ZP2 (B(max) approximately 500 000 sites per sperm; K(d) approximately 200 nM). Use of unlabeled ZP3, ZP2, and ZP1 as competitive inhibitors of the binding of fluorochrome-labeled ZP3 and ZP2 demonstrated that ZP3 and ZP2 bound specifically to their respective sites on sperm. Finally, we demonstrate that extracellular calcium as well as capacitation and maturation of sperm are required for these sites to bind their respective ligands.

摘要

有大量证据表明,小鼠受精需要精子与构成透明带(ZP)的三种糖蛋白中的两种(ZP3和ZP2)结合。尽管这种结合具有生物学重要性,但没有人证明精子表达针对ZP3和ZP2的独立、可饱和且特异性的结合位点。这样的证明是定义精子上ZP3和ZP2结合位点的分布、数量、亲和力和功能调节的先决条件。本文报道的实验使用荧光染料标记的ZP3和ZP2以及定量图像分析来表征ZP3和ZP2与活的、获能的、顶体完整的小鼠精子上不同位点的可饱和结合。大约20%的ZP3结合位点位于顶体帽上,其余位点位于头部的顶体后区域。相比之下,仅在顶体后区域检测到ZP2结合位点。饱和分析估计了ZP3(B(max)约为每个精子185000个位点;K(d)约为67 nM)和ZP2(B(max)约为每个精子500000个位点;K(d)约为200 nM)结合位点的数量和亲和力。使用未标记的ZP3、ZP2和ZP1作为荧光染料标记的ZP3和ZP2结合的竞争性抑制剂,证明ZP3和ZP2特异性结合到精子上各自的位点。最后,我们证明这些位点结合其各自配体需要细胞外钙以及精子的获能和成熟。

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