Optical control of AMPA receptors using a photoswitchable quinoxaline-2,3-dione antagonist

被引:38
作者
Barber, David M. [1 ,2 ]
Liu, Shu-An [1 ,2 ]
Gottschling, Kevin [3 ]
Sumser, Martin [1 ,2 ]
Hollmann, Michael [3 ]
Trauner, Dirk [1 ,2 ]
机构
[1] Ludwig Maximilians Univ Munchen, Dept Chem, Butenandtstr 5-13, D-81377 Munich, Germany
[2] Ludwig Maximilians Univ Munchen, Ctr Integrated Prot Sci, Butenandtstr 5-13, D-81377 Munich, Germany
[3] Ruhr Univ Bochum, Dept Biochem Receptor Biochem 1, D-44780 Bochum, Germany
基金
欧洲研究理事会;
关键词
IONOTROPIC GLUTAMATE RECEPTORS; PHOTOCHROMIC AGONIST; NMDA RECEPTORS; BLIND MICE; INHIBITORS; ACETYLCHOLINESTERASE; NEUROPROTECTION; PHARMACOLOGY;
D O I
10.1039/c6sc01621a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
AMPA receptors respond to the neurotransmitter glutamate and play a critical role in excitatory neurotransmission. They have been implicated in several psychiatric disorders and have rich pharmacology. Antagonists of AMPA receptors have been explored as drugs and one has even reached the clinic. We now introduce a freely diffusible photoswitchable antagonist that is selective for AMPA receptors and endows them with light-sensitivity. Our photoswitch, ShuBQX-3, is active in its dark-adapted trans-isoform but is significantly less active as its cis-isoform. ShuBQX-3 exhibits a remarkable red-shifting of its photoswitching properties through interactions with the AMPA receptor ligand binding site. Since it can be used to control action potential firing with light, it could emerge as a powerful tool for studying synaptic transmission with high spatial and temporal precision.
引用
收藏
页码:611 / 615
页数:5
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