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
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