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通过自身抗独特型方法制备的腺苷受体单克隆抗体。

Monoclonal antibodies to adenosine receptor by an auto-anti-idiotypic approach.

作者信息

Ku H H, Cleveland W L, Erlanger B F

机构信息

Department of Microbiology, College of Physicians and Surgeons, Columbia University, New York, NY 10032.

出版信息

J Immunol. 1987 Oct 1;139(7):2376-84.

PMID:3655366
Abstract

Monoclonal antiadenosine receptor antibodies have been raised by an auto-anti-idiotypic approach. BALB/c mice were immunized with adenosine 6-aminocaproyl-bovine serum albumin. Hybridoma cell lines were raised and lines that secreted antibodies that bound to rabbit antiadenosine antibodies were obtained. Two such monoclonal antibodies, AA18 and AA21, were studied in detail and found to be directed at adenosine receptors by the following criteria. They inhibited the binding of [3H] adenosine to rabbit antiadenosine antibodies that had binding characteristics similar to those of adenosine receptors. They bound to rat brain membranes and binding could be inhibited by N6-cyclohexyladenosine and L-N6-phenylisopropyladenosine, both adenosine receptor agonists. They also inhibited the binding of [3H]L-N6-phenylisopropyladenosine to rat brain membranes. In functional assays, they inhibited adenylate cyclase of rat brain membranes, but had no effect on adenylate cyclase of rat hepatic membranes, indicating that they mimic agonists of the A1 receptor, therefore, carrying an "internal image" of the adenosine molecule. When adenosine receptors of rat brain membranes were solubilized with 1% cholic acid, partially purified on an adenosine 6-aminocaproyl AH-Sepharose column and analyzed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and Western blotting, both AA18 and AA21 recognized a 62,000 band under nonreducing conditions, and a major band of 36,000 under reducing conditions. We conclude that the auto-anti-idiotypic route has yielded specific antibodies that recognize the A1 adenosine receptor.

摘要

通过自身抗独特型方法制备了单克隆抗腺苷受体抗体。用腺苷6-氨基己酰-牛血清白蛋白免疫BALB/c小鼠。培养杂交瘤细胞系,获得分泌与兔抗腺苷抗体结合的抗体的细胞系。对两种这样的单克隆抗体AA18和AA21进行了详细研究,并根据以下标准发现它们针对腺苷受体。它们抑制[3H]腺苷与具有与腺苷受体相似结合特性的兔抗腺苷抗体的结合。它们与大鼠脑膜结合,并且结合可被N6-环己基腺苷和L-N6-苯基异丙基腺苷这两种腺苷受体激动剂抑制。它们还抑制[3H]L-N6-苯基异丙基腺苷与大鼠脑膜的结合。在功能测定中,它们抑制大鼠脑膜的腺苷酸环化酶,但对大鼠肝细胞膜的腺苷酸环化酶没有影响,表明它们模拟A1受体激动剂,因此携带腺苷分子的“内影像”。当用1%胆酸溶解大鼠脑膜的腺苷受体,在腺苷6-氨基己酰AH-琼脂糖柱上进行部分纯化,并通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳和蛋白质印迹分析时,AA18和AA21在非还原条件下均识别出一条62,000的条带,在还原条件下识别出一条主要的36,000的条带。我们得出结论,自身抗独特型途径产生了识别A1腺苷受体的特异性抗体。

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