共 50 条
Relationship between ligand binding and YIPP motif in the C-terminal region of human AT1 receptor
被引:6
|作者:
Inada, Y
[1
]
Nakane, T
[1
]
Chiba, S
[1
]
机构:
[1] Shinshu Univ, Dept Pharmacol, Sch Med, Matsumoto, Nagano 3908621, Japan
来源:
关键词:
AT(1);
receptor;
YIPP motif;
radioligand-binding assay;
confocal laser-scanning microscopy;
Western blot;
intracellular Ca2+ mobilization;
D O I:
10.1016/S0167-4889(02)00400-7
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
The YIPP (tyrosine-isoleucine-proline-proline, amino acids 319-322) motif within the C-terminal part of the human AT(1) receptor is associated with angiotensin II (AII)-induced activation of the Jak-STAT pathway and phospholipase Cgamma1 phosphorylation. We report here that mutations of the YIPP motif strongly affect ligand-binding to the receptor. We analysed AT(1) receptors of the wild type (WT) and 11 mutants with a FLAG-epitope-tag within their C-terminal portion. Mutations of the "P-P" amino acid sequence of this motif decreased both AII binding and the AII-induced intracellular Ca2+ transients. Mutant and WT receptors were expressed equally in the cell membrane and were localized within the plasma membrane. These results suggest that the "P-P" amino acid sequence within the YIPP motif is important for AII binding to the AT(1) receptor. (C) 2003 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:33 / 41
页数:9
相关论文