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Fractionation of mycobacterial integral membrane proteins by continuous elution SDS–PAGE reveals the immunodominance of low molecular weight subunits for human T cells

机译:通过连续洗脱SDS-PAGE分离分枝杆菌整合膜蛋白揭示了人类T细胞的低分子量亚基的免疫优势

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摘要

Integral membrane proteins (IMP) represent a serologically distinct class of mycobacterial antigens which are potent stimulators of human T cells (Mehrotra et al., Clin Exp Immunol 1995; >102:626). The range of IMP from Mycobacterium fortuitum was resolved by continuous elution SDS–PAGE to recover 31 discrete fractions covering bands up to ≈ 58 kD. The fractions, after removal of SDS, were subjected to human T cell proliferation assays for the identification of immunodominant molecule(s). A low molecular weight (<20kD) fraction was able to stimulate T cells from 11 out of 12 donors comprising mainly tuberculoid leprosy patients. The described protocol is well suited to situations where large quantities of antigenic protein mixtures must be processed in order to get the purified molecules/fractions in amounts required for immunoepidemiological studies.
机译:整合膜蛋白(IMP)代表了一种分型在血清学上不同的分枝杆菌抗原,它们是人类T细胞的有效刺激剂(Mehrotra等人,Clin Exp Immunol 1995; > 102 :626)。通过连续洗脱SDS-PAGE解析了来自分枝杆菌的IMP范围,以回收31个离散片段,覆盖了约≈58 kD的条带。除去SDS后,将级分进行人T细胞增殖测定,以鉴定免疫显性分子。低分子量(<20kD)馏分能够刺激主要由结核性麻风病人组成的12个捐献者中的11个T细胞。所描述的方案非常适用于必须处理大量抗原蛋白混合物才能获得免疫流行病学研究所需量的纯化分子/馏分的情况。

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