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针对盘基网柄菌钙调蛋白的单克隆抗体的制备及其特异性

Production and specificity of monoclonal antibodies against calmodulin from Dictyostelium discoideum.

作者信息

Hulen D, Baron A, Salisbury J, Clarke M

机构信息

Program in Molecular and Cell Biology, Oklahoma Medical Research Foundation, Oklahoma City 73104.

出版信息

Cell Motil Cytoskeleton. 1991;18(2):113-22. doi: 10.1002/cm.970180206.

Abstract

Monoclonal antibodies were raised against calmodulin purified from Dictyostelium discoideum. To increase its antigenicity, the calmodulin was conjugated to keyhole limpet hemocyanin; mice were immunized with the conjugate. Hybridomas producing antibodies against calmodulin were identified by screening culture supernatants with calmodulin coupled to bovine serum albumin. The specificity of antibodies from hybridoma culture supernatants was tested by Western blot of Dictyostelium cell lysates. For the purpose, methods were developed that permitted sensitive detection of calmodulin bound to membranes. The key elements of the blotting protocol were used of PVDF membrane, transfer conducted in phosphate buffer, and glutaraldehyde fixation after transfer. These methods permitted detection of as little as 0.1 ng of calmodulin spotted directly onto the membrane, or 10 ng transferred from an SDS polyacrylamide gel. Ten calmodulin-specific antibodies were identified; most of these reacted preferentially with the calcium-containing form of Dictyostelium calmodulin. Several of the monoclonal antibodies cross-reacted with calmodulin from bovine brain.

摘要

制备了针对从盘基网柄菌中纯化得到的钙调蛋白的单克隆抗体。为增强其抗原性,将钙调蛋白与匙孔血蓝蛋白偶联;用该偶联物免疫小鼠。通过用与牛血清白蛋白偶联的钙调蛋白筛选培养上清液,鉴定出产生抗钙调蛋白抗体的杂交瘤。通过对盘基网柄菌细胞裂解物进行蛋白质免疫印迹,检测杂交瘤培养上清液中抗体的特异性。为此,开发了能够灵敏检测与膜结合的钙调蛋白的方法。蛋白质印迹方案的关键要素包括使用聚偏二氟乙烯膜、在磷酸盐缓冲液中进行转印以及转印后用戊二醛固定。这些方法能够检测到直接点样在膜上低至0.1 ng的钙调蛋白,或从SDS聚丙烯酰胺凝胶中转印的10 ng钙调蛋白。鉴定出了十种钙调蛋白特异性抗体;其中大多数优先与盘基网柄菌钙调蛋白的含钙形式发生反应。几种单克隆抗体与牛脑钙调蛋白发生交叉反应。

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