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豚鼠精子顶体外膜:分离与结构表征

Outer acrosomal membrane of guinea pig spermatozoa: isolation and structural characterization.

作者信息

Olson G E, Winfrey V P, Winer M A, Davenport G R

机构信息

Department of Cell Biology, Vanderbilt University School of Medicine, Nashville, Tennessee 37232.

出版信息

Gamete Res. 1987 May;17(1):77-94. doi: 10.1002/mrd.1120170109.

Abstract

We describe a protocol to isolate a highly enriched fraction of outer acrosomal membrane from guinea pig spermatozoa and present new data on the ultrastructure of this membrane domain. Cauda epididymal spermatozoa were suspended into a low ionic strength buffer and subjected to brief homogenization; this stripped the plasma membrane from the spermatozoa and severed the acrosomal apical segment from the spermatozoon. The crescent-shaped apical segments retained the outer acrosomal membrane and specific components of the acrosomal matrix. Enriched fractions of apical segments were isolated on discontinuous sucrose gradients and the outer acrosomal membrane purified by subsequent centrifugation onto Percoll density gradients. The isolated outer acrosomal membrane did not form vesicles, but instead rolled up into spiral sheets. Both thin section and negatively stained specimens revealed a paracrystalline arrangement of filaments associated with the luminal surface of the membrane. The isolated outer acrosomal membrane revealed a limited number of polypeptides by SDS-PAGE, and the polypeptide pattern was distinct from the plasma membrane fraction. The isolated acrosomal membranes possessed no ouabain sensitive Na+,K+-ATPase activity, whereas about 20% of the ATPase activity of the plasma membrane enriched fraction was inhibited by ouabain. The potential function of the structural differentiations of the outer acrosomal membrane in the membrane fusion events of the acrosome reaction is discussed.

摘要

我们描述了一种从豚鼠精子中分离出高度富集的顶体外膜组分的方法,并展示了关于该膜结构域超微结构的新数据。附睾尾部精子被悬浮于低离子强度缓冲液中并进行短暂匀浆;这使精子的质膜被剥离,并将顶体顶端节段从精子上切断。新月形的顶端节段保留了顶体外膜和顶体基质的特定成分。通过不连续蔗糖梯度分离出富集的顶端节段组分,并通过随后在Percoll密度梯度上离心来纯化顶体外膜。分离出的顶体外膜未形成囊泡,而是卷成螺旋状薄片。超薄切片和负染标本均显示与膜腔表面相关的细丝呈准晶体排列。通过SDS-PAGE分析,分离出的顶体外膜显示出有限数量的多肽,且多肽图谱与质膜组分不同。分离出的顶体膜不具有哇巴因敏感的Na⁺,K⁺-ATP酶活性,而质膜富集组分约20%的ATP酶活性可被哇巴因抑制。文中讨论了顶体外膜结构分化在顶体反应膜融合事件中的潜在功能。

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