Katagiri Yohko U, Kiyokawa Nobutaka, Nakamura Kyoko, Takenouchi Hisami, Taguchi Tomoko, Okita Hajime, Umezawa Akihiro, Fujimoto Junichiro
Department of Developmental Biology, National Research Institute for Child Health and Development, Setagaya-ku, Tokyo 157-8535, Japan.
Biochem Biophys Res Commun. 2005 Jul 15;332(4):1004-11. doi: 10.1016/j.bbrc.2005.05.052.
We previously produced monoclonal antibodies against the detergent-insoluble microdomain, i.e., the raft microdomain, of the human renal cancer cell line ACHN. Raft.2, one of these monoclonal antibodies, recognizes sialosyl globopentaosylceramide, which has the stage-specific embryonic antigen (SSEA)-4 epitope. Although the mouse embryonal carcinoma (EC) cell line F9 does not express SSEA-4, some F9 cells stained with Raft.2. Western analysis and matrix-assisted laser desorption ionization-time of flight mass spectrometry identified the Raft.2 binding molecule as laminin binding protein (LBP), i.e., 34/67 laminin receptor. Weak acid treatment or digestion with Clostridium perfringens sialidase reduced Raft.2 binding to LBP on nitrocellulose sheets and [(14)C]galactose was incorporated into LBP, indicating LBP to have a sialylated carbohydrate moiety. Subcellular localization analysis by sucrose density-gradient centrifugation and examination by confocal microscopy revealed LBP to be localized on the outer surface of the plasma membrane. An SSEA-4-positive human EC cell line, NCR-G3 cells, also expressed Raft.2-binding LBP.
我们之前制备了针对人肾癌细胞系ACHN去污剂不溶性微结构域(即脂筏微结构域)的单克隆抗体。其中一种单克隆抗体Raft.2可识别具有阶段特异性胚胎抗原(SSEA)-4表位的唾液酸化球戊糖神经酰胺。尽管小鼠胚胎癌细胞(EC)系F9不表达SSEA-4,但一些F9细胞可被Raft.2染色。蛋白质免疫印迹分析和基质辅助激光解吸电离飞行时间质谱鉴定出Raft.2结合分子为层粘连蛋白结合蛋白(LBP),即34/67层粘连蛋白受体。弱酸处理或用产气荚膜梭菌唾液酸酶消化可减少Raft.2与硝酸纤维素膜上LBP的结合,并且[¹⁴C]半乳糖掺入LBP中,表明LBP具有唾液酸化碳水化合物部分。通过蔗糖密度梯度离心进行的亚细胞定位分析和共聚焦显微镜检查显示LBP定位于质膜外表面。一种SSEA-4阳性的人EC细胞系NCR-G3细胞也表达Raft.2结合的LBP。