Suppr超能文献

针对肿瘤相关抗原的可磷酸化单克隆抗体的构建

Construction of phosphorylatable monoclonal antibody to a tumor-associated antigen.

作者信息

Lin L, Daugherty B, Schlom J, Pestka S

机构信息

Department of Molecular Genetics and Microbiology, University of Medicine and Dentistry of New Jersey, Robert Wood Johnson Medical School, Piscataway 08854-5635, USA.

出版信息

Cancer Res. 1996 Sep 15;56(18):4250-4.

PMID:8797600
Abstract

A phosphorylation site was introduced into chimeric monoclonal antibody B72.3 (MAb-chB72.3) by site-specific mutation of the coding sequence. The phosphorylation site for the cAMP-dependent protein kinase was positioned at the carboxyl terminus of the heavy-chain constant region of MAb-chB72.3. The resultant modified MAb-chB72.3-P was expressed in 293 cells and purified. The MAb-chB72.3-P protein was phosphorylated by the catalytic subunit of cAMP-dependent protein kinase with [gamma-32P]ATP to high radiospecific activity. The 32P-labeled MAb-chB72.3-P protein bound to cells expressing the tumor-associated glycoprotein 72 antigen. The introduction of phosphorylation sites into MAbs provides a new type of MAb for the diagnosis and treatment of cancers.

摘要

通过对编码序列进行位点特异性突变,在嵌合单克隆抗体B72.3(MAb-chB72.3)中引入了一个磷酸化位点。环磷酸腺苷(cAMP)依赖性蛋白激酶的磷酸化位点位于MAb-chB72.3重链恒定区的羧基末端。所得的修饰型MAb-chB72.3-P在293细胞中表达并纯化。MAb-chB72.3-P蛋白被cAMP依赖性蛋白激酶的催化亚基用[γ-32P]ATP磷酸化,达到高放射比活性。32P标记的MAb-chB72.3-P蛋白与表达肿瘤相关糖蛋白72抗原的细胞结合。在单克隆抗体中引入磷酸化位点为癌症的诊断和治疗提供了一种新型的单克隆抗体。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验