{"title":"用于体外凝结物形成和客户分化试验的色粒素 B 纯化。","authors":"Anup Parchure, Julia Von Blume","doi":"10.21769/BioProtoc.5095","DOIUrl":null,"url":null,"abstract":"<p><p>Chromogranin B and other members of the granin protein family form condensates that recruit clients like proinsulin. The condensation in the lumen of <i>trans</i>-Golgi network (TGN) is critical for the biogenesis of secretory granules. Here, we describe a protocol to purify the tagged version of chromogranin B close to its native form at the TGN, which can then be utilized for microscopy-based assays to monitor condensate formation in vitro and client partitioning depending on the material properties of chromogranin B assemblies. Key features • First instance of purification of full-length and tagged version of members of the chromogranin family of proteins. • Allows purification of proteins with post-translational modifications that are acquired en route in the secretory pathway, thus closely resembling their native form at the TGN.</p>","PeriodicalId":93907,"journal":{"name":"Bio-protocol","volume":null,"pages":null},"PeriodicalIF":1.0000,"publicationDate":"2024-10-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11540053/pdf/","citationCount":"0","resultStr":"{\"title\":\"Chromogranin B Purification for Condensate Formation and Client Partitioning Assays In Vitro.\",\"authors\":\"Anup Parchure, Julia Von Blume\",\"doi\":\"10.21769/BioProtoc.5095\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Chromogranin B and other members of the granin protein family form condensates that recruit clients like proinsulin. The condensation in the lumen of <i>trans</i>-Golgi network (TGN) is critical for the biogenesis of secretory granules. Here, we describe a protocol to purify the tagged version of chromogranin B close to its native form at the TGN, which can then be utilized for microscopy-based assays to monitor condensate formation in vitro and client partitioning depending on the material properties of chromogranin B assemblies. Key features • First instance of purification of full-length and tagged version of members of the chromogranin family of proteins. • Allows purification of proteins with post-translational modifications that are acquired en route in the secretory pathway, thus closely resembling their native form at the TGN.</p>\",\"PeriodicalId\":93907,\"journal\":{\"name\":\"Bio-protocol\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":1.0000,\"publicationDate\":\"2024-10-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11540053/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Bio-protocol\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.21769/BioProtoc.5095\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bio-protocol","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.21769/BioProtoc.5095","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"BIOLOGY","Score":null,"Total":0}
引用次数: 0
摘要
Chromogranin B 和粒蛋白家族的其他成员会形成凝集物,吸引胰岛素等客户。在跨高尔基体网络(TGN)管腔中的凝集对于分泌颗粒的生物生成至关重要。在此,我们介绍了一种纯化嗜铬粒蛋白 B 标记版本的方案,该标记版本接近其在 TGN 的原生形式,然后可用于基于显微镜的检测,以监测体外凝集物的形成以及根据嗜铬粒蛋白 B 集合的材料特性进行的客户分区。主要特点 - 首次纯化全长和标记的嗜铬粒蛋白家族成员。- 可纯化在分泌途径中获得翻译后修饰的蛋白质,因此与其在 TGN 的原生形式非常相似。
Chromogranin B Purification for Condensate Formation and Client Partitioning Assays In Vitro.
Chromogranin B and other members of the granin protein family form condensates that recruit clients like proinsulin. The condensation in the lumen of trans-Golgi network (TGN) is critical for the biogenesis of secretory granules. Here, we describe a protocol to purify the tagged version of chromogranin B close to its native form at the TGN, which can then be utilized for microscopy-based assays to monitor condensate formation in vitro and client partitioning depending on the material properties of chromogranin B assemblies. Key features • First instance of purification of full-length and tagged version of members of the chromogranin family of proteins. • Allows purification of proteins with post-translational modifications that are acquired en route in the secretory pathway, thus closely resembling their native form at the TGN.