Morris S L, Rouse D A, Hussong D, Chaparas S D
Center for Biologics Evaluation and Research, Food and Drug Administration, Bethesda, Maryland 20892.
Infect Immun. 1990 Jan;58(1):17-20. doi: 10.1128/iai.58.1.17-20.1990.
Four bacteriophages expressing different immunoreactive recombinant Mycobacterium intracellulare antigens were isolated from a lambda gt11 library with monoclonal antibodies to M. intracellulare. These four antibodies reacted with native M. intracellulare proteins of 54, 43, 40/38, and 22 kilodaltons. Southern blot hybridizations with DNA probes prepared from insert fragments of these bacteriophages confirmed the M. intracellulare derivation of the inserts. The physical maps of the immunoreactive phages were deduced by restriction enzyme digestions. The molecular weights of the expressed recombinant antigens were determined by Western (immuno-) blotting.
用抗胞内分枝杆菌的单克隆抗体从λgt11文库中分离出四种表达不同免疫反应性重组胞内分枝杆菌抗原的噬菌体。这四种抗体与54、43、40/38和22千道尔顿的天然胞内分枝杆菌蛋白发生反应。用从这些噬菌体的插入片段制备的DNA探针进行Southern印迹杂交,证实了插入片段来源于胞内分枝杆菌。通过限制性酶切推断出免疫反应性噬菌体的物理图谱。通过Western(免疫)印迹法测定表达的重组抗原的分子量。