Swanwick Catherine Croft, Shapiro Marietta E, Yi Zhaohong, Chang Kai, Wenthold Robert J
Laboratory of Neurochemistry, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, MD 20892, USA.
FEBS Lett. 2009 Apr 17;583(8):1226-30. doi: 10.1016/j.febslet.2009.03.017. Epub 2009 Mar 17.
N-methyl-D-aspartate receptors (NMDARs) mediate excitatory synaptic transmission in the brain. Here we demonstrate interactions between the NR2A and NR2B subunits of NMDARs with flotillin-1 (flot-1), a lipid raft-associated protein. When mapped, analogous regions in the far distal C-termini of NR2A and NR2B mediate binding to flot-1, and the prohibitin homology domain of flot-1 contains binding sites for NR2A and NR2B. Although NR2B can also directly bind to flot-2 via a separate region of its distal C-terminus, NMDARs were significantly more colocalized with flot-1 than flot-2 in cultured hippocampal neurons. Overall, this study defines a novel interaction between NMDARs and flotillins.
N-甲基-D-天冬氨酸受体(NMDARs)介导大脑中的兴奋性突触传递。在此,我们展示了NMDARs的NR2A和NR2B亚基与小窝蛋白-1(flot-1)之间的相互作用,小窝蛋白-1是一种与脂筏相关的蛋白质。经定位,NR2A和NR2B远末端C末端的类似区域介导与flot-1的结合,且flot-1的禁阻素同源结构域含有NR2A和NR2B的结合位点。尽管NR2B也可通过其远端C末端的一个单独区域直接与flot-2结合,但在培养的海马神经元中,NMDARs与flot-1的共定位显著多于与flot-2的共定位。总体而言,本研究确定了NMDARs与小窝蛋白之间的一种新型相互作用。