Yin Y
Department of Bacteriology, School of Medicine, Osaka City University.
Kansenshogaku Zasshi. 1994 Nov;68(11):1330-7. doi: 10.11150/kansenshogakuzasshi1970.68.1330.
I have constructed the genomic library of M. leprae Thai 53 strain, and cloned the alpha antigen like protein gene by plaque hybridization method by using M. leprae alpha antigen DNA fragment as probe which was characterized in the previous study, I have termed it as alpha 2 antigen gene. The alpha 2 antigen gene has been characterized by sequencing. By comparing the deduced amino acid sequence of alpha and alpha 2 antigen with 85 complex antigen of other mycobacteria. I have found the higher homology between alpha 2 antigen and 85A antigen and between alpha antigen and 85B antigen. We have constructed the over expression system of M. leprae alpha and alpha 2 antigen gene in E. coli using vector pMALc-RI. Recombinant alpha and alpha 2 antigen has been purified by amylose column chromatography at the purity of more than 95%. More than 6 mg and more than 10 mg of recombinant alpha and alpha 2 antigen has been obtained from 200 ml of liquid culture, respectively. ELISA tests have been performed with the sera of leprosy patient and healthy control against the recombinant alpha and alpha 2 antigens. The antibody titers in sera of leprosy patient against the two kinds of antigens were all much higher than healthy controls. The antibody titer against the alpha 2 antigen was higher than that against alpha antigen. Recombinant alpha and alpha 2 antigens in this study could be used as a new specific antigen for serodiagnosis of leprosy.
我构建了麻风杆菌泰国53株的基因组文库,并以前期研究中鉴定的麻风杆菌α抗原DNA片段为探针,通过噬菌斑杂交法克隆了α抗原样蛋白基因,我将其命名为α2抗原基因。α2抗原基因已通过测序进行了鉴定。通过将α和α2抗原推导的氨基酸序列与其他分枝杆菌的85种复合抗原进行比较,我发现α2抗原与85A抗原之间以及α抗原与85B抗原之间具有较高的同源性。我们使用载体pMALc-RI在大肠杆菌中构建了麻风杆菌α和α2抗原基因的过表达系统。重组α和α2抗原已通过直链淀粉柱层析纯化,纯度超过95%。分别从200 ml液体培养物中获得了超过6 mg和超过10 mg的重组α和α2抗原。用麻风病患者和健康对照的血清对重组α和α2抗原进行了ELISA检测。麻风病患者血清中针对这两种抗原的抗体滴度均远高于健康对照。针对α2抗原的抗体滴度高于针对α抗原的抗体滴度。本研究中的重组α和α2抗原可作为麻风病血清学诊断的新的特异性抗原。