{"title":"人恶性黑色素瘤废培养基中HLA-DR抗原的浮选和密度分离两步富集。","authors":"M J Khosravi, S K Liao","doi":"10.3109/08820138309050759","DOIUrl":null,"url":null,"abstract":"<p><p>HLA-DR antigens released by cultured human melanoma cells were harvested from spent medium. Antigenic activity was monitored by quantitative absorption analysis in the mixed hemadsorption assay using anti-HLA-DR rabbit antiserum. Following concentration by amicon filtration, and removal of insoluble components by centrifugation at 136,000 g, the spent medium was subjected to KBr (density, 1.23 g/ml) flotation. The antigenic material was enriched in the upper one-third fraction (lipoprotein-rich), by a factor of 7 with 79% recovery. Further purification of this upper fraction by sucrose (5-30%) density gradient resulted in a marked increase in antigenic activity in the bottom fraction (No. 6), by a factor of 167 with 56% recovery from the spent medium concentrate. Thus, these procedures offer a promising approach towards the isolation of HLA-DR antigens from shed material of cultured melanoma cells for further purification and structural studies.</p>","PeriodicalId":13417,"journal":{"name":"Immunological communications","volume":"12 4","pages":"387-96"},"PeriodicalIF":0.0000,"publicationDate":"1983-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.3109/08820138309050759","citationCount":"2","resultStr":"{\"title\":\"Two-step enrichment of HLA-DR antigens from spent medium of human malignant melanoma culture by flotation and density separation procedures.\",\"authors\":\"M J Khosravi, S K Liao\",\"doi\":\"10.3109/08820138309050759\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>HLA-DR antigens released by cultured human melanoma cells were harvested from spent medium. Antigenic activity was monitored by quantitative absorption analysis in the mixed hemadsorption assay using anti-HLA-DR rabbit antiserum. Following concentration by amicon filtration, and removal of insoluble components by centrifugation at 136,000 g, the spent medium was subjected to KBr (density, 1.23 g/ml) flotation. The antigenic material was enriched in the upper one-third fraction (lipoprotein-rich), by a factor of 7 with 79% recovery. Further purification of this upper fraction by sucrose (5-30%) density gradient resulted in a marked increase in antigenic activity in the bottom fraction (No. 6), by a factor of 167 with 56% recovery from the spent medium concentrate. Thus, these procedures offer a promising approach towards the isolation of HLA-DR antigens from shed material of cultured melanoma cells for further purification and structural studies.</p>\",\"PeriodicalId\":13417,\"journal\":{\"name\":\"Immunological communications\",\"volume\":\"12 4\",\"pages\":\"387-96\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1983-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.3109/08820138309050759\",\"citationCount\":\"2\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Immunological communications\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.3109/08820138309050759\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Immunological communications","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3109/08820138309050759","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Two-step enrichment of HLA-DR antigens from spent medium of human malignant melanoma culture by flotation and density separation procedures.
HLA-DR antigens released by cultured human melanoma cells were harvested from spent medium. Antigenic activity was monitored by quantitative absorption analysis in the mixed hemadsorption assay using anti-HLA-DR rabbit antiserum. Following concentration by amicon filtration, and removal of insoluble components by centrifugation at 136,000 g, the spent medium was subjected to KBr (density, 1.23 g/ml) flotation. The antigenic material was enriched in the upper one-third fraction (lipoprotein-rich), by a factor of 7 with 79% recovery. Further purification of this upper fraction by sucrose (5-30%) density gradient resulted in a marked increase in antigenic activity in the bottom fraction (No. 6), by a factor of 167 with 56% recovery from the spent medium concentrate. Thus, these procedures offer a promising approach towards the isolation of HLA-DR antigens from shed material of cultured melanoma cells for further purification and structural studies.