Clark B R, Mills B J, Horikoshi K, Shively J E, Todd C W
J Immunol Methods. 1984 Mar 16;67(2):371-7. doi: 10.1016/0022-1759(84)90476-9.
A method for the facile removal of mitogens or inducers of lymphokine production from cell culture medium of stimulated cells is described. The technique is based on the covalent attachment of biotin to mitogen or inducer and the removal of the biotinylated products from stimulated cell culture medium using immobilized avidin. Using this procedure, biotin-labeled staphylococcal enterotoxin A (SEA-B) was shown not to differ significantly from unmodified SEA in its capacity to stimulate mitogenesis and induce production of immune interferon (IFN) and T-cell growth factor (TCGF) in cultures of human mononuclear cells from peripheral blood. SEA-B was also shown not to differ from SEA in its binding to SEA antibodies. Results of mitogenicity studies and competitive radioimmune assay (RIA) measurements indicate that SEA-B is essentially completely removed from stimulated cell culture medium by absorption with avidin coupled to Sepharose 4B.
本文描述了一种从受刺激细胞的细胞培养基中轻松去除丝裂原或淋巴因子产生诱导剂的方法。该技术基于生物素与丝裂原或诱导剂的共价连接,以及使用固定化抗生物素蛋白从受刺激细胞培养基中去除生物素化产物。使用该程序,生物素标记的葡萄球菌肠毒素A(SEA-B)在刺激外周血人单核细胞培养物中的有丝分裂原活性、诱导免疫干扰素(IFN)和T细胞生长因子(TCGF)产生的能力方面,与未修饰的SEA没有显著差异。SEA-B与SEA抗体结合的情况也显示无差异。有丝分裂原活性研究和竞争性放射免疫分析(RIA)测量结果表明,通过与琼脂糖4B偶联的抗生物素蛋白吸收,SEA-B基本上能从受刺激细胞培养基中完全去除。