Kudo A, Nishimura Y, Watanabe T
J Immunol. 1985 Jul;135(1):642-5.
We have cloned a rearranged immunoglobulin heavy chain variable (VH) region gene (NL-1-H-5) from the cells of a mouse hybridoma, NL-1, which produce a monoclonal antibody against the common acute lymphocytic leukemia (cALL) antigen. The DNA base sequence of NL-1-H-5 clone revealed that the VH region gene of NL-1 cells used the identical or closely related leader (L) and VH gene to those of the myeloma cell line MOPC-21. There were seven base differences, and six of them were found in the second complementary-determining hypervariable region (CDR-2). The five nucleotide differences in CDR-2 resulted in the variation of amino acid residues of positions 54, 56, 58, and 59. In particular, nucleotide changes at position 56 and 59 yielded tyrosine residues which might be involved in a part of the antibody-combining site structure for cALL antigen.
我们从小鼠杂交瘤NL-1的细胞中克隆出了一个重排的免疫球蛋白重链可变(VH)区基因(NL-1-H-5),该杂交瘤产生一种针对常见急性淋巴细胞白血病(cALL)抗原的单克隆抗体。NL-1-H-5克隆的DNA碱基序列显示,NL-1细胞的VH区基因使用了与骨髓瘤细胞系MOPC-21相同或密切相关的前导(L)基因和VH基因。存在七个碱基差异,其中六个位于第二个互补决定高变区(CDR-2)。CDR-2中的五个核苷酸差异导致了第54、56、58和59位氨基酸残基的变化。特别是,第56和59位的核苷酸变化产生了酪氨酸残基,这可能参与了针对cALL抗原的抗体结合位点结构的一部分。