| FEBS Letters | |
| A new phosphoglycerolipid, ‘phosphatidylglucose’, found in human cord red cells by multi‐reactive monoclonal anti‐i cold agglutinin, mAb GL‐1/GL‐2 | |
| Nagatsuka, Yasuko2  Uzawa, Jun4  Hirabayashi, Yoshio5  Ono, Yasushi2  Shimizu, Kazufumi2  Ohashi, Yoko3  Kasama, Takeshi1  | |
| [1] Laboratory of Biochemical Analysis, Tokyo Medical and Dental University, Tokyo, Japan;Department of Immunology and Microbiology, Nihon University School of Medicine, 30-1 Oyaguchikami-machi, Itabashi-ku, Tokyo 173-8610, Japan;Frontier Research Program, The Institute of Physical and Chemical Research, Tokyo, Japan;Division of Molecular Characterisation, The Institute of Physical and Chemical Research, Tokyo, Japan;Brain Science Institute, The Institute of Physical and Chemical Research, Tokyo, Japan | |
| 关键词: Epstein–Barr virus; Human monoclonal antibody; Cold agglutinin; Cord red cell; Glycolipid; EBV; Epstein–Barr virus; PLA; C and D; phospholipase A; C and D; PI-PLC; phosphatidylinositol-specific phospholipase C; TLC; thin layer chromatography; SIMS; secondary ion mass spectrum; CID; collision-induced dissociation; TOCSY; total correlation spectroscopy; | |
| DOI : 10.1016/S0014-5793(01)02464-4 | |
| 学科分类:生物化学/生物物理 | |
| 来源: John Wiley & Sons Ltd. | |
PDF
|
|
【 摘 要 】
Cord red cell membranes express many differentiation-related molecules. To study such molecules, we have established human cell lines, termed GL-1 and GL-2, by the Epstein–Barr virus transformation method, both of which produce monoclonal anti-i cold agglutinin [Y. Nagatsuka et al., Immunol. Lett. 46 (1995) 93–100]. Thin layer chromatography immunoblotting analysis revealed that these antibodies had broad specificities reacting with a variety of glycolipid antigens. Of the immunoreactive lipid antigens, a new phosphoglycerolipid containing glucose from human cord red cells was found. The isolated lipid was unstable to alkaline hydrolysis and contained glucose as a sole sugar. Secondary ion mass spectrum–collision-induced dissociation mass spectrometric analysis of this lipid gave the main molecular ion peak at m/z 885 corresponding to phosphatidylhexose. This antigen was susceptible to phospholipases A2, C and D but resistant to phosphatidylinositol-specific phospholipase C. Two-dimensional nuclear magnetic resonance spectroscopy confirmed that glucose is linked to the sn-glycerol 3-phosphate residue with a β-anomeric configuration. Based upon these combined results, we identified this lipid as phosphatidyl-β-D-glucose. This is the first report showing the presence of the glucosylated glycerophospholipid in mammalian sources.
【 授权许可】
Unknown
【 预 览 】
| Files | Size | Format | View |
|---|---|---|---|
| RO201912020310568ZK.pdf | 538KB |
PDF