Suppr超能文献

用于特异性和灵敏监测酪蛋白激酶-1和-2的两种新型肽底物的设计与合成。

Design and synthesis of two new peptide substrates for the specific and sensitive monitoring of casein kinases-1 and -2.

作者信息

Marin O, Meggio F, Pinna L A

机构信息

Dipartimento di Chimica Biologica, CRIBI and CNR, Università di Padova, Italy.

出版信息

Biochem Biophys Res Commun. 1994 Feb 15;198(3):898-905. doi: 10.1006/bbrc.1994.1128.

Abstract

The available information about the specificity determinants of casein kinases-1 and -2 (CK1 and CK2) has been utilized to obtain two new peptide substrates optimally suited for the specific monitoring of these two pleiotropic enzymes. The best substrate developed for CK1 is the inhibitor-2 derived peptide RRKDLHDDEEDEAMSITA which is superior in every respect to all the non phosphorylated CK1 peptide substrates used so far. Its Km is 172 microM and the Vmax is 6-fold higher than that of casein. The dodecapeptide RRRADDSDDDDD, on the other hand, is totally refractory to CK1 while it is an excellent substrate for CK2, exhibiting, under basal conditions, a Km value of 19 microM and a Vmax higher than those obtained with all the routinely used substrates of CK2. Both the novel CK1 and CK2 peptide substrates are suited for the phosphocellulose paper assay.

摘要

已利用酪蛋白激酶-1和-2(CK1和CK2)特异性决定因素的现有信息,获得了两种最适合特异性监测这两种多效性酶的新肽底物。为CK1开发的最佳底物是抑制剂-2衍生肽RRKDLHDDEEDEAMSITA,在各个方面都优于迄今为止使用的所有非磷酸化CK1肽底物。其Km为172微摩尔,Vmax比酪蛋白高6倍。另一方面,十二肽RRRADDSDDDDD对CK1完全无反应,而它是CK2的优良底物,在基础条件下,Km值为19微摩尔,Vmax高于用CK2所有常规使用底物获得的值。新型CK1和CK2肽底物均适用于磷酸纤维素纸分析法。

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