Sharon J, Gefter M L, Manser T, Morrison S L, Oi V T, Ptashne M
Nature. 1984;309(5966):364-7. doi: 10.1038/309364a0.
The heavy (H) and light (L) chains of antibodies consist of variable (V) and constant (C) regions. The V regions of the heavy and light chains form the antibody combining site. To determine whether a V region could be functional when joined to a polypeptide other than its own C region, we constructed a chimaeric gene encoding the V region of a mouse heavy chain and the C region of a mouse kappa light chain ( VHC kappa). The heavy-chain gene is derived from an A/J mouse hybridoma cell line 36-65 whose antibody product (gamma 1, kappa) is specific for the hapten azophenylarsonate. We report here that, when introduced into a mouse myeloma cell line, the chimaeric gene is expressed and a protein of the expected molecular weight is secreted into the medium. As light chains tend to dimerize we expected that the VHC kappa protein might associate with light chain from the cell line 36-65 to form an antibody-binding molecule. Affinity binding experiments and Ka determination indicate that this is the case. Dimers of this type offer a novel and interesting alternative to existing antibody-binding molecules.
抗体的重链(H)和轻链(L)由可变区(V)和恒定区(C)组成。重链和轻链的V区形成抗体结合位点。为了确定一个V区与自身C区以外的多肽连接时是否具有功能,我们构建了一个嵌合基因,该基因编码小鼠重链的V区和小鼠κ轻链的C区(VHCκ)。重链基因来源于A/J小鼠杂交瘤细胞系36-65,其抗体产物(γ1,κ)对半抗原偶氮苯胂酸具有特异性。我们在此报告,当将该嵌合基因导入小鼠骨髓瘤细胞系时,它会表达,并且预期分子量的蛋白质会分泌到培养基中。由于轻链倾向于二聚化,我们预期VHCκ蛋白可能会与细胞系36-65的轻链结合形成抗体结合分子。亲和结合实验和亲和力常数测定表明情况确实如此。这种二聚体为现有的抗体结合分子提供了一种新颖有趣的替代物。