Hipfner D R, Gauldie S D, Deeley R G, Cole S P
Cancer Research Laboratories, Queen's University, Kingston, Ontario, Canada.
Cancer Res. 1994 Nov 15;54(22):5788-92.
MRP is a M(r) 190,000 integral membrane phosphoglycoprotein that is overexpressed in some drug-selected resistant cell lines and has been shown to cause multidrug resistance in transfected cells. Five murine hybridoma cell lines (QCRL-1, QCRL-2, QCRL-3, QCRL-4, and QCRL-6) have been generated which secrete monoclonal antibodies (MAbs) that react specifically with membrane proteins of MRP-overexpressing, multidrug-resistant, drug-selected H69AR cells and MRP-transfected HeLa cells (T5) but not the respective parental (H69) and vector-transfected (C1) cells. The ability of three of these MAbs (QCRL-1, QCRL-2, and QCRL-3) to selectively immunoprecipitate a M(r) 190,000 protein from 35S-labeled H69AR and T5 membranes indicates that these MAbs are specific for MRP. MAb QCRL-1 is also capable of detecting the low levels of MRP present in revertant H69PR cells by immunoblot analysis. Indirect immunofluorescence analyses show that MAbs QCRL-1, QCRL-2, and QCRL-3) strongly and differentially react with fixed T5 and H69AR cells but not with unfixed cells, suggesting that these MAbs recognize intracellular MRP epitopes. The availability of reagents for the specific and sensitive immunodetection of MRP should greatly facilitate biological and clinical studies of this novel drug resistance protein.
多药耐药相关蛋白(MRP)是一种分子量为190,000的整合膜磷酸糖蛋白,在一些经药物筛选的耐药细胞系中过度表达,并且已证实在转染细胞中可导致多药耐药。现已构建了五种鼠杂交瘤细胞系(QCRL-1、QCRL-2、QCRL-3、QCRL-4和QCRL-6),它们分泌的单克隆抗体(MAb)能与过度表达MRP的多药耐药、经药物筛选的H69AR细胞以及MRP转染的HeLa细胞(T5)的膜蛋白特异性反应,但不与各自的亲本细胞(H69)和载体转染细胞(C1)反应。其中三种单克隆抗体(QCRL-1、QCRL-2和QCRL-3)能够从35S标记的H69AR和T5细胞膜中选择性免疫沉淀出分子量为190,000的蛋白,这表明这些单克隆抗体对MRP具有特异性。单克隆抗体QCRL-1还能够通过免疫印迹分析检测到回复性H69PR细胞中存在的低水平MRP。间接免疫荧光分析表明,单克隆抗体QCRL-1、QCRL-2和QCRL-3)与固定的T5细胞和H69AR细胞强烈且有差异地反应,但不与未固定细胞反应,这表明这些单克隆抗体识别细胞内MRP表位。用于MRP特异性和灵敏免疫检测的试剂的可得性应极大地促进对这种新型耐药蛋白的生物学和临床研究。