Garbe T, Harris D, Vordermeier M, Lathigra R, Ivanyi J, Young D
Medical Research Council Tuberculosis and Related Infections Unit, Royal Postgraduate Medical School, Hammersmith Hospital, London, United Kingdom.
Infect Immun. 1993 Jan;61(1):260-7. doi: 10.1128/iai.61.1.260-267.1993.
The gene encoding a 19-kDa antigen from Mycobacterium tuberculosis was expressed as a recombinant protein in the rapid-growing species Mycobacterium smegmatis. The recombinant antigen was expressed at a level approximately ninefold higher than in M. tuberculosis and, like the native antigen, was found in the pellet fraction after high-speed centrifugation of bacterial extracts. The 19-kDa antigen in crude bacterial extracts, and the purified recombinant antigen, bound strongly to concanavalin A, indicating the possibility of posttranslational glycosylation. The recombinant antigen stimulated T-cell proliferation in vitro when added to assays either in the form of whole recombinant bacteria or as a purified protein. Homologous expression of mycobacterial antigens in a rapid-growing mycobacterial host may be particularly useful for the immunological characterization of proteins which are subject to posttranslational modification.
结核分枝杆菌中编码19 kDa抗原的基因在快速生长的耻垢分枝杆菌中表达为重组蛋白。该重组抗原的表达水平比在结核分枝杆菌中高约九倍,并且与天然抗原一样,在细菌提取物高速离心后的沉淀部分中被发现。粗细菌提取物中的19 kDa抗原和纯化的重组抗原与伴刀豆球蛋白A强烈结合,表明存在翻译后糖基化的可能性。当以完整重组细菌的形式或作为纯化蛋白添加到检测中时,该重组抗原在体外刺激T细胞增殖。在快速生长的分枝杆菌宿主中同源表达分枝杆菌抗原对于对经历翻译后修饰的蛋白质进行免疫学表征可能特别有用。