glutamate receptor 2; GluR-2; GluR-B; GluR-K2; glutamate receptor ionotropic, AMPA 2; AMPA-selective glutamate receptor 2 (GRIA2, GLUR2)
Jump to navigation
Jump to search
Function
- ionotropic glutamate receptor
- binding of the excitatory neurotransmitter L-glutamate induces a conformation change, leading to the opening of the cation channel, & thereby converts the chemical signal to an electrical impulse
- the receptor then desensitizes rapidly & enters a transient inactive state, characterized by the presence of bound agonist
- palmitoylated
- depalmitoylated upon glutamate stimulation
- Cys-610 palmitoylation leads to Golgi retention & decreased cell surface expression
- in contrast, Cys-836 palmitoylation does not affect cell surface expression but regulates stimulation- dependent endocytosis (putative)
- may interact with MPP4
- interacts with PRKCABP, GRIP1 & GRIP2
- forms a ternary complex with GRIP1 & CSPG4
- binds to PDZ domain of GRIP1 via C-terminal SVKI motif
- receptor binds AMPA (quisqualate) > glutamate > kainate
Structure
- homotetramer or heterotetramer of pore-forming glutamate receptor subunits
- tetramers may be formed by the dimerization of dimer
- belongs to the glutamate-gated ion channel (TC 1.A.10) family
Compartment
Alternative splicing
named isoforms=3
Genetics
- RNA editing: modified positions=607
- partially edited
- fully edited in brain
- heteromerically expressed edited GLUR2 (R) receptor complexes are impermeable to Ca+2, whereas the unedited (Q) forms are highly permeable to divalent ions