{"title":"Sperm-Binding Assay Using an In Vitro 3D Model of the Mammalian Cumulus-Oocyte Complex","authors":"Julieta Gabriela Hamze, María Jiménez-Movilla, Raquel Romar","doi":"10.1002/cptx.100","DOIUrl":null,"url":null,"abstract":"<p>We have recently described a new model to study gamete interaction in mammalian species. The model recreates the spherical surface of the oocyte by using magnetic Sepharose beads coated with a layer of a recombinant protein involved in gamete interaction (such as ZP2, or the IZUMO1 receptor JUNO) and an external layer of <i>cumulus oophorus</i> cells, thus mimicking, to some extent, a native cumulus-oocyte complex. Once generated, this 3D model can be used in a sperm-binding assay to obtain valuable information about the molecular basis of gamete interaction, since different recombinant proteins can be used to coat the bead surface, thus generating a variety of models to be used for several species. Furthermore, thanks to the ability of the model to decoy sperm, the physiological status of the bound sperm can be studied, making this a powerful tool to select sperm with high fertilizing capacity, to unmask subfertile animals in livestock breeding centers, or for toxicological studies. Here, we describe how to generate and use this model for sperm-binding assays, using porcine sperm as an example, and ZP2, a protein from zona pellucida, as the recombinant protein of interest. © 2020 Wiley Periodicals LLC.</p><p><b>Basic Protocol 1</b>: Generation of the in vitro 3D model</p><p><b>Alternate Protocol 1</b>: Binding <i>cumulus oophorus</i> cells to the model</p><p><b>Basic Protocol 2</b>: Quality control of the model by SDS-PAGE electrophoresis and western blot</p><p><b>Support Protocol 1</b>: Immunochemistry to confirm proper protein distribution on surface of beads</p><p><b>Support Protocol 2</b>: Elution of recombinant conjugated proteins</p><p><b>Basic Protocol 3</b>: Sperm-binding assay</p><p><b>Alternate Protocol 2</b>: Sperm preparation by the swim-up method</p>","PeriodicalId":72743,"journal":{"name":"Current protocols in toxicology","volume":"86 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2020-12-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/cptx.100","citationCount":"2","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current protocols in toxicology","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cptx.100","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 2
Abstract
We have recently described a new model to study gamete interaction in mammalian species. The model recreates the spherical surface of the oocyte by using magnetic Sepharose beads coated with a layer of a recombinant protein involved in gamete interaction (such as ZP2, or the IZUMO1 receptor JUNO) and an external layer of cumulus oophorus cells, thus mimicking, to some extent, a native cumulus-oocyte complex. Once generated, this 3D model can be used in a sperm-binding assay to obtain valuable information about the molecular basis of gamete interaction, since different recombinant proteins can be used to coat the bead surface, thus generating a variety of models to be used for several species. Furthermore, thanks to the ability of the model to decoy sperm, the physiological status of the bound sperm can be studied, making this a powerful tool to select sperm with high fertilizing capacity, to unmask subfertile animals in livestock breeding centers, or for toxicological studies. Here, we describe how to generate and use this model for sperm-binding assays, using porcine sperm as an example, and ZP2, a protein from zona pellucida, as the recombinant protein of interest. © 2020 Wiley Periodicals LLC.
Basic Protocol 1: Generation of the in vitro 3D model
Alternate Protocol 1: Binding cumulus oophorus cells to the model
Basic Protocol 2: Quality control of the model by SDS-PAGE electrophoresis and western blot
Support Protocol 1: Immunochemistry to confirm proper protein distribution on surface of beads
Support Protocol 2: Elution of recombinant conjugated proteins
Basic Protocol 3: Sperm-binding assay
Alternate Protocol 2: Sperm preparation by the swim-up method
利用哺乳动物卵丘-卵母细胞复合体的体外3D模型进行精子结合试验
我们最近描述了一个研究哺乳动物物种配子相互作用的新模型。该模型通过磁性Sepharose珠包被一层参与配子相互作用的重组蛋白(如ZP2,或IZUMO1受体JUNO)和卵丘细胞的外层来重建卵母细胞的球形表面,从而在一定程度上模仿了天然的卵丘-卵母细胞复合物。一旦生成,该3D模型可用于精子结合试验,以获得有关配子相互作用的分子基础的有价值的信息,因为不同的重组蛋白可用于覆盖头表面,从而生成用于不同物种的各种模型。此外,由于该模型具有诱骗精子的能力,因此可以研究结合精子的生理状态,使其成为选择具有高受精能力的精子,在牲畜育种中心揭开低生育能力动物的面纱或进行毒理学研究的有力工具。在这里,我们描述了如何生成和使用该模型进行精子结合分析,以猪精子为例,并将来自透明带的蛋白ZP2作为感兴趣的重组蛋白。©2020 Wiley期刊有限责任公司基本方案1:体外3D模型的生成备用方案1:将卵积云细胞结合到模型上基本方案2:通过SDS-PAGE电泳和western blot对模型进行质量控制支持方案1:免疫化学以确认珠表面适当的蛋白质分布支持方案2:重组偶联蛋白洗脱基本方案3:精子结合测定备用方案2:通过游泳法制备精子
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