Functional partnerships between GPI-anchored proteins and adhesion GPCRs

被引:1
|
作者
Lin, Hsi-Hsien [1 ,2 ,3 ,4 ,5 ]
机构
[1] Chang Gung Univ, Coll Med, Dept Microbiol & Immunol, Taoyuan, Taiwan
[2] Chang Gung Univ, Coll Med, Grad Sch Biomed Sci, Taoyuan, Taiwan
[3] Chang Gung Mem Hosp Linkou, Dept Anat Pathol, Taoyuan, Taiwan
[4] Chang Gung Mem Hosp Keelung, Div Rheumatol Allergy & Immunol, Keelung, Taiwan
[5] Chang Gung Univ, Dept Microbiol & Immunol, Coll Med, Taoyuan 33302, Taiwan
关键词
adhesion GPCR; GPI-anchored protein; ligand; receptor; signalosome; BRAIN-BARRIER INTEGRITY; COUPLED RECEPTOR; CNS ANGIOGENESIS; LIGAND CD55; CELL POLARITY; SCHWANN-CELLS; PRION PROTEIN; NOGO RECEPTOR; GPR126; CD97;
D O I
10.1002/bies.202300115
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
Specific extracellular interaction between glycophosphatidylinositol (GPI)-anchored proteins and adhesion G protein-coupled receptors (aGPCRs) plays an important role in unique biological functions. GPI-anchored proteins are derived from a novel post-translational modification of single-span membrane molecules, while aGPCRs are bona fide seven-span transmembrane proteins with a long extracellular domain. Although various members of the two structurally-distinct protein families are known to be involved in a wide range of biological processes, many remain as orphans. Interestingly, accumulating evidence has pointed to a complex interaction and functional synergy between these two protein families. I discuss herein current understanding of specific functional partnerships between GPI-anchored proteins and aGPCRs.
引用
收藏
页数:12
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