Reddy B M, Karande A A, Adiga P R
Centre for Reproductive Biology and Molecular Endocrinology, Indian Institute of Science, Bangalore.
Mol Immunol. 1993 Oct;30(15):1355-60. doi: 10.1016/0161-5890(93)90096-t.
Monoclonal antibodies raised against human serum retinol-binding protein (hRBP) were used as probes for the study of the antigenic determinants of hRBP and those shared with the same protein from other species. The antibodies could be classified into four distinct groups and react with the homologous proteins from the rat as well as the rabbit sera. Three of these antibodies recognize sequential or continuous epitopes while the remaining antibody is directed against a discontinuous or conformational epitope. By chemical cleavage with cyanogen bromide, the domains recognized by the monoclonal antibodies could be delineated. By solid-phase synthetic approach, the core sequences recognized by two of these monoclonal antibodies were identified to amino acid sequences 45-51 and 128-131 of the primary amino acid sequence of hRBP.
针对人血清视黄醇结合蛋白(hRBP)产生的单克隆抗体被用作探针,以研究hRBP的抗原决定簇以及与其他物种相同蛋白质共有的抗原决定簇。这些抗体可分为四个不同的组,并与大鼠以及兔血清中的同源蛋白发生反应。其中三种抗体识别连续或线性表位,而其余抗体则针对不连续或构象表位。通过溴化氰化学裂解,可以勾勒出单克隆抗体识别的结构域。通过固相合成方法,确定了其中两种单克隆抗体识别的核心序列为hRBP一级氨基酸序列的45-51和128-131氨基酸序列。