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抗人碳酸酐酶III单克隆抗体的制备与特性分析

Production and characterization of monoclonal antibodies to human carbonic anhydrase III.

作者信息

Azzazy H M, Cummings P J, Ambrozak D R, Christenson R H

机构信息

Department of Medical and Research Technology, University of Maryland School of Medicine, Baltimore 21201, USA.

出版信息

Hybridoma. 1998 Dec;17(6):553-8. doi: 10.1089/hyb.1998.17.553.

Abstract

Carbonic anhydrase III (CAIII) is a cytosolic protein found almost exclusively in slow-oxidative skeletal muscle fibers. Upon excessive skeletal muscle activity or damage, CAIII is rapidly released into serum. CAIII is not found in cardiac muscle, whereas the muscle protein myoglobin (Myo) is found in skeletal and cardiac muscle. Because CAIII and Myo are released from injured muscle in a constant ratio, an increase in the Myo/CAIII ratio may be useful as an early diagnostic indicator of acute myocardial damage. Although several reliable Myo immunoassays have been established, no similar CAIII immunoassay is commercially available. We produced murine monoclonal antibodies (MAbs) to human CAIII using standard immunization and cell fusion procedures. Using an enzyme-linked immunoadsorbent assay (ELISA), three MAbs showed strong immunoreactivity with CAIII, but low to moderate levels of cross-reactivity with closely related isoenzymes CAI and CAII. The three MAbs demonstrated unique patterns of reactivity toward CAI, CAII, and CAIII, suggesting that different CAIII epitopes are recognized by the three MAbs. Specificity was further examined by Western blot analysis. These MAbs demonstrated potential for use in the development of an immunoassay for CAIII, and for investigating the biology of skeletal muscle injury in vivo.

摘要

碳酸酐酶III(CAIII)是一种几乎仅在慢氧化型骨骼肌纤维中发现的胞质蛋白。在骨骼肌过度活动或受损时,CAIII会迅速释放到血清中。心肌中未发现CAIII,而肌肉蛋白肌红蛋白(Myo)在骨骼肌和心肌中均有发现。由于CAIII和Myo从受损肌肉中以恒定比例释放,Myo/CAIII比值的增加可能作为急性心肌损伤的早期诊断指标。尽管已经建立了几种可靠的Myo免疫测定方法,但尚无类似的CAIII免疫测定方法可供商业使用。我们使用标准免疫和细胞融合程序制备了针对人CAIII的鼠单克隆抗体(MAb)。使用酶联免疫吸附测定(ELISA),三种MAb与CAIII表现出强免疫反应性,但与密切相关的同工酶CAI和CAII的交叉反应性低至中等水平。这三种MAb对CAI、CAII和CAIII表现出独特的反应模式,表明这三种MAb识别不同的CAIII表位。通过蛋白质印迹分析进一步检测特异性。这些MAb显示出用于开发CAIII免疫测定方法以及研究体内骨骼肌损伤生物学的潜力。

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