Tyrosine phosphorylation of the nicotinic acetylcholine receptor (AChR) is associated with an altered rate of receptor desensitization and also may play a role in agrin-induced receptor clustering. We have demonstrated a previously unsuspected interaction between Torpedo AChR and the adaptor protein Grb2. The binding is mediated by the Src homology 2 (SH2) domain of Grb2 and the tyrosine-phosphorylated delta subunit of the AChR. Dephosphorylation of the delta subunit abolishes Grb2 binding. A cytoplasmic domain of the delta subunit contains a binding motif (pYXNX) for the SH2 domain of Grb2. Indeed, a phosphopeptide corresponding to this region of the delta subunit binds to Grb2 SH2 fusion proteins with relatively high affinity, whereas a peptide lacking phosphorylation on tyrosine exhibits no binding. Grb2 is colocalized with the AChR on the innervated face of Torpedo electrocytes. Furthermore, Grb2 specifically copurifies with AChR solubilized from postsynaptic membranes. These data suggest a novel role for tyrosine phosphorylation of the AChR in the initiation of a Grb2-mediated signaling cascade at the postsynaptic membrane.

译文

烟碱乙酰胆碱受体 (AChR) 的酪氨酸磷酸化与受体脱敏率的改变有关,并且也可能在agrin诱导的受体聚集中起作用。我们已经证明了鱼雷AChR和衔接蛋白grb2之间以前未曾怀疑的相互作用。结合由Grb2的Src同源2 (SH2) 结构域和AChR的酪氨酸磷酸化 δ 亚基介导。Δ 亚基的去磷酸化消除了Grb2结合。Δ 亚基的细胞质结构域包含grb2的SH2结构域的结合基序 (pYXNX)。实际上,对应于 δ 亚基该区域的磷酸肽以相对较高的亲和力与Grb2 SH2融合蛋白结合,而在酪氨酸上缺乏磷酸化的肽则没有结合。Grb2与AChR共定位在鱼雷细胞的神经支配面上。此外,Grb2与溶解于突触后膜的AChR特异性共聚。这些数据表明,AChR的酪氨酸磷酸化在突触后膜的Grb2-mediated信号级联反应的启动中起着新的作用。

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