André C, Guillet J G, De Backer J P, Vanderheyden P, Hoebeke J, Strosberg A D
EMBO J. 1984 Jan;3(1):17-21. doi: 10.1002/j.1460-2075.1984.tb01755.x.
BALB/c mice were immunized with affinity-purified muscarinic acetylcholine receptors from calf brain and their splenocytes fused with NS1 myeloma cells. Hybrid cultures were grown and selected for production of antibodies on the basis of enzyme immunoassays on calf and rat forebrain membrane preparations. Thirty-four clones were retained and six of them further subcloned. Two of these subclones produced antibodies that selectively recognized muscarinic acetylcholine receptor-bearing membranes. The M-35b antibodies interacted only with native digitonin-solubilized receptors, and not with denatured receptors. The M-23c antibodies did not react with active digitonin-solubilized receptors but recognized the denatured form. The M-23c antibodies should thus be useful in the purification of the receptor and its precursor translation products, while the M-35b antibodies could be used for the immunocytochemical localization of the receptor in cells and tissues of different species.
用从小牛脑中亲和纯化的毒蕈碱型乙酰胆碱受体免疫BALB/c小鼠,然后将其脾细胞与NS1骨髓瘤细胞融合。培养杂交细胞,并根据对小牛和大鼠前脑膜制剂的酶免疫测定法筛选产生抗体的细胞。保留了34个克隆,其中6个进一步亚克隆。这些亚克隆中的两个产生了能选择性识别携带毒蕈碱型乙酰胆碱受体的膜的抗体。M-35b抗体仅与天然洋地黄皂苷溶解的受体相互作用,而不与变性受体相互作用。M-23c抗体不与活性洋地黄皂苷溶解的受体反应,但能识别变性形式。因此,M-23c抗体可用于受体及其前体翻译产物的纯化,而M-35b抗体可用于在不同物种的细胞和组织中对受体进行免疫细胞化学定位。