{"title":"利用金免疫标记技术对肌营养不良蛋白的超微结构定位。","authors":"M J Cullen, J Walsh, L V Nicholson, J B Harris","doi":"10.1098/rspb.1990.0034","DOIUrl":null,"url":null,"abstract":"<p><p>Immunolabelling with a 5 nm gold probe was used to localize dystrophin at the ultrastructural level in human muscle. The primary antibody was monoclonal, raised against a segment (amino acids 1181-1388) from the rod domain of dystrophin. The antibody (Dy4/6D3) is specific for dystrophin and shows no immunoreactivity with any protein from mdx mouse muscle or from patients with a gene deletion spanning part of the molecule recognized by the antibody (Nicholson et al. 1989 a; England et al. 1990). Using this antibody, labelling was almost entirely confined to a narrow 75 nm rim at the periphery of the muscle fibres. Histograms of the distance from the gold probe to the cytoplasmic face of the plasma membrane and of the distance between gold probes (nearest neighbour in a plane parallel with the plasma membrane) displayed modes at approximately 15 nm and 120 nm, respectively. The distribution of the probe was the same in longitudinal and transverse sections of the muscle. These observations suggest that the rod portion of the dystrophin molecule is normally arranged close to the cytoplasmic face of the plasma membrane and that the molecules form an interconnecting network. Labelling was not associated with the transverse tubular system.</p>","PeriodicalId":54561,"journal":{"name":"Proceedings of the Royal Society of London Series B-Containing Papers of Abiological Character","volume":"240 1297","pages":"197-210"},"PeriodicalIF":0.0000,"publicationDate":"1990-05-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1098/rspb.1990.0034","citationCount":"119","resultStr":"{\"title\":\"Ultrastructural localization of dystrophin in human muscle by using gold immunolabelling.\",\"authors\":\"M J Cullen, J Walsh, L V Nicholson, J B Harris\",\"doi\":\"10.1098/rspb.1990.0034\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Immunolabelling with a 5 nm gold probe was used to localize dystrophin at the ultrastructural level in human muscle. The primary antibody was monoclonal, raised against a segment (amino acids 1181-1388) from the rod domain of dystrophin. The antibody (Dy4/6D3) is specific for dystrophin and shows no immunoreactivity with any protein from mdx mouse muscle or from patients with a gene deletion spanning part of the molecule recognized by the antibody (Nicholson et al. 1989 a; England et al. 1990). Using this antibody, labelling was almost entirely confined to a narrow 75 nm rim at the periphery of the muscle fibres. Histograms of the distance from the gold probe to the cytoplasmic face of the plasma membrane and of the distance between gold probes (nearest neighbour in a plane parallel with the plasma membrane) displayed modes at approximately 15 nm and 120 nm, respectively. The distribution of the probe was the same in longitudinal and transverse sections of the muscle. These observations suggest that the rod portion of the dystrophin molecule is normally arranged close to the cytoplasmic face of the plasma membrane and that the molecules form an interconnecting network. Labelling was not associated with the transverse tubular system.</p>\",\"PeriodicalId\":54561,\"journal\":{\"name\":\"Proceedings of the Royal Society of London Series B-Containing Papers of Abiological Character\",\"volume\":\"240 1297\",\"pages\":\"197-210\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1990-05-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1098/rspb.1990.0034\",\"citationCount\":\"119\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Proceedings of the Royal Society of London Series B-Containing Papers of Abiological Character\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1098/rspb.1990.0034\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Proceedings of the Royal Society of London Series B-Containing Papers of Abiological Character","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1098/rspb.1990.0034","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 119
摘要
用5 nm金探针免疫标记,在超微结构水平上定位肌营养不良蛋白。一抗为单克隆抗体,针对抗肌营养不良蛋白杆状结构域的一段(氨基酸1181 ~ 1388)产生。该抗体(Dy4/6D3)对肌营养不良蛋白具有特异性,对mdx小鼠肌肉中的任何蛋白或抗体识别的部分分子中存在基因缺失的患者均无免疫反应性(Nicholson et al. 1989 a;England et al. 1990)。使用该抗体,标记几乎完全局限于肌纤维外围狭窄的75 nm边缘。从金探针到质膜细胞质表面的距离直方图和金探针之间的距离直方图(与质膜平行的平面上最近的邻居)分别显示了大约15 nm和120 nm的模式。探针在肌肉纵、横切面的分布相同。这些观察结果表明,肌营养不良蛋白分子的杆状部分通常排列在靠近质膜的细胞质面,并且这些分子形成一个相互连接的网络。标记与横管系统无关。
Ultrastructural localization of dystrophin in human muscle by using gold immunolabelling.
Immunolabelling with a 5 nm gold probe was used to localize dystrophin at the ultrastructural level in human muscle. The primary antibody was monoclonal, raised against a segment (amino acids 1181-1388) from the rod domain of dystrophin. The antibody (Dy4/6D3) is specific for dystrophin and shows no immunoreactivity with any protein from mdx mouse muscle or from patients with a gene deletion spanning part of the molecule recognized by the antibody (Nicholson et al. 1989 a; England et al. 1990). Using this antibody, labelling was almost entirely confined to a narrow 75 nm rim at the periphery of the muscle fibres. Histograms of the distance from the gold probe to the cytoplasmic face of the plasma membrane and of the distance between gold probes (nearest neighbour in a plane parallel with the plasma membrane) displayed modes at approximately 15 nm and 120 nm, respectively. The distribution of the probe was the same in longitudinal and transverse sections of the muscle. These observations suggest that the rod portion of the dystrophin molecule is normally arranged close to the cytoplasmic face of the plasma membrane and that the molecules form an interconnecting network. Labelling was not associated with the transverse tubular system.