{"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}
引用次数: 2
Abstract
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.