Suppr超能文献

合成磺脲类药物与胰岛素瘤细胞系MIN6特异性结合的探究。

Probing of specific binding of synthetic sulfonylurea with the insulinoma cell line MIN6.

作者信息

Park Keun-Hong, Akaike Toshihiro

机构信息

College of Medicine, Pochon CHA University, Cell and Gene Therapy Research Institute 605, Yeoksam 1-dong, Kangnam-gu, Seoul 135-081, Korea.

出版信息

J Biochem. 2005 Jul;138(1):21-5. doi: 10.1093/jb/mvi103.

Abstract

To overcome the limitation of conventional sulfonylurea (SU) for investigation of biological mechanisms related to KATP channels, a hypoglycemic sulfonylurea (SU) was conjugated with a non-reducing glucose bearing polystyrene (PS) derivative to provide enhanced interaction with an insulinoma cell line (MIN6). The specific interaction between the SU (K+ channel closer)-conjugated copolymer and MIN6 cells was confirmed by confocal laser microscopic images using rhodamine B isothiocyanate (RITC)-labeled SU-conjugated polymer, which revealed the specific interaction between SU-conjugated polymer and MIN6 cells. Moreover, the location of labeled polymer and the site of Ca2+ ion mobilization obtained from the same MIN6 cells were identical. Based on the specificity and insulinotropic activity, the SU-conjugated polymer is expected to be useful tool for the study of biological mechanisms of KATP channels.

摘要

为克服传统磺脲类药物(SU)在研究与KATP通道相关生物学机制方面的局限性,将一种降糖磺脲类药物与一种带有非还原葡萄糖的聚苯乙烯(PS)衍生物偶联,以增强与胰岛素瘤细胞系(MIN6)的相互作用。使用异硫氰酸罗丹明B(RITC)标记的SU偶联聚合物,通过共聚焦激光显微镜图像证实了SU(K+通道关闭剂)偶联共聚物与MIN6细胞之间的特异性相互作用,该图像显示了SU偶联聚合物与MIN6细胞之间的特异性相互作用。此外,从同一MIN6细胞获得的标记聚合物的位置与Ca2+离子动员的位点相同。基于其特异性和促胰岛素活性,SU偶联聚合物有望成为研究KATP通道生物学机制的有用工具。

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