Nair E R, Banerjee S, Kumar S, Reddy M V, Harinath B C
Jamnalal Bajaj Tropical Disease Research Centre and Department of Biochemistry, Mahatma Gandhi, Institute of Medical Sciences, Sevagram, 442 102 Wardha, Maharashtra India.
Indian J Clin Biochem. 2001 Jan;16(1):132-5. doi: 10.1007/BF02867583.
Proteins secreted into the culture medium byMycobacterium tuberculosis (M. tb) are shown to be source of antigens of immunodiagnostic interest. Anin vitro released 31 kDa antigen ESAS-7F isolated fromM.tb H(37)Ra culture filtrate by salt precipitation, SDS-PAGE and cation exchange fast protein liquid chromatography (FPLC) was shown earlier to be a diagnostically important antigen fraction. In this report, we describe the isolation of ESAS-7F antigen using monospecific antibody coupled to sepharose CL-4B column. The percentage recovery of ESAS-7F antigen using affinity chromatography was approximately 8% of the total ES antigen proteins compared to 0.05% obtained by conventional purification steps using salt precipitation, SDS-PAGE and FPLC. Similar seroreactivity was observed by the antigen isolated by both the methods in indirect ELISA. Affinity chromatography helped in an increased recovery of ESAS-7F antigen and obviates the need for time consuming conventional purification steps.
结核分枝杆菌(M. tb)分泌到培养基中的蛋白质被证明是具有免疫诊断意义的抗原来源。通过盐沉淀、SDS-PAGE和阳离子交换快速蛋白质液相色谱(FPLC)从M. tb H(37)Ra培养滤液中分离出的一种体外释放的31 kDa抗原ESAS-7F,早前已被证明是一种具有诊断重要性的抗原组分。在本报告中,我们描述了使用偶联到琼脂糖CL-4B柱上的单特异性抗体分离ESAS-7F抗原的方法。与使用盐沉淀、SDS-PAGE和FPLC的传统纯化步骤获得的0.05%相比,使用亲和色谱法获得的ESAS-7F抗原回收率约为ES抗原总蛋白的8%。两种方法分离得到的抗原在间接ELISA中观察到相似的血清反应性。亲和色谱有助于提高ESAS-7F抗原的回收率,并且无需耗时的传统纯化步骤。