Abastado J P, Jaulin C, Schutze M P, Langlade-Demoyen P, Plata F, Ozato K, Kourilsky P
J Exp Med. 1987 Aug 1;166(2):327-40. doi: 10.1084/jem.166.2.327.
11 intradomain recombinants between H-2Kd and H-2Dd were produced using an original technique based on in vivo recombination in Escherichia coli. After transfection into mouse L cells, all these recombinants were expressed at high levels on the cell surface. The specificities of 77 mAbs were examined on these cell lines. mAbs could be organized in 12 groups. In each group, a small number of amino acids participating in the recognized epitope(s) were identified. In a few instances, noncontinuous epitopes comprising amino acids belonging to different domains of the antigen were found. The data thus obtained are compatible with those produced in previous exon-shuffling experiments, but permit a much more precise definition of recognized epitope(s).
利用一种基于大肠杆菌体内重组的原创技术,产生了11个H-2Kd和H-2Dd之间的结构域内重组体。转染到小鼠L细胞后,所有这些重组体均在细胞表面高水平表达。在这些细胞系上检测了77种单克隆抗体的特异性。单克隆抗体可分为12组。在每组中,鉴定出了参与识别表位的少数氨基酸。在少数情况下,发现了由属于抗原不同结构域的氨基酸组成的不连续表位。由此获得的数据与先前外显子改组实验产生的数据相符,但能更精确地定义识别的表位。