Bodmer J, Bodmer W, Heyes J, So A, Tonks S, Trowsdale J, Young J
Proc Natl Acad Sci U S A. 1987 Jul;84(13):4596-600. doi: 10.1073/pnas.84.13.4596.
Thirty-four lymphoblastoid cell lines that had been previously typed for HLA-DP antigens by primed lymphocyte typing (PLT) were tested by Southern blotting and by ELISA. Using two DP beta probes and a DP alpha probe with a series of enzymes, it is possible to identify restriction fragment length polymorphism (RFLP) patterns characteristic of DPw1, -2, -3, -4, and possibly -5. ELISA typing results, based on two polymorphic DP antibodies DP11.1 and ILR1, were compared with PLT-defined and RFLP-defined types. Thus, using a range of probes and enzymes it is possible to identify DP polymorphism. The value of monoclonal antibodies for such studies is demonstrated, and the molecular data can, in some cases, pinpoint the amino acids responsible for the specificity of the monoclonal antibodies.
通过Southern印迹法和酶联免疫吸附测定(ELISA)对之前用启动淋巴细胞分型法(PLT)进行HLA - DP抗原分型的34个淋巴母细胞系进行了检测。使用两种DPβ探针和一种DPα探针以及一系列酶,能够识别出DPw1、-2、-3、-4以及可能的-5所特有的限制性片段长度多态性(RFLP)模式。基于两种多态性DP抗体DP11.1和ILR1的ELISA分型结果,与PLT定义的类型和RFLP定义的类型进行了比较。因此,使用一系列探针和酶能够识别DP多态性。证明了单克隆抗体在这类研究中的价值,并且在某些情况下分子数据能够确定负责单克隆抗体特异性的氨基酸。