Sine Steven M, Shen Xing-Ming, Wang Hai-Long, Ohno Kinji, Lee Won-Yong, Tsujino Akira, Brengmann Joan, Bren Nina, Vajsar Jiri, Engel Andrew G
Receptor Biology Laboratory, Department of Physiology and Biophysics, and Mayo Foundation, Rochester, MN 55905, USA.
J Gen Physiol. 2002 Oct;120(4):483-96. doi: 10.1085/jgp.20028568.
By defining functional defects in a congenital myasthenic syndrome (CMS), we show that two mutant residues, located in a binding site region of the acetylcholine receptor (AChR) epsilon subunit, exert opposite effects on ACh binding and suppress channel gating. Single channel kinetic analysis reveals that the first mutation, epsilon N182Y, increases ACh affinity for receptors in the resting closed state, which promotes sequential occupancy of the binding sites and discloses rate constants for ACh occupancy of the nonmutant alphadelta site. Studies of the analogous mutation in the delta subunit, deltaN187Y, disclose rate constants for ACh occupancy of the nonmutant alpha epsilon site. The second CMS mutation, epsilon D175N, reduces ACh affinity for receptors in the resting closed state; occupancy of the mutant site still promotes gating because a large difference in affinity is maintained between closed and open states. epsilon D175N impairs overall gating, however, through an effect independent of ACh occupancy. When mapped on a structural model of the AChR binding site, epsilon N182Y localizes to the interface with the alpha subunit, and epsilon D175 to the entrance of the ACh binding cavity. Both epsilon N182Y and epsilon D175 show state specificity in affecting closed relative to desensitized state affinities, suggesting that the protein chain harboring epsilon N182 and epsilon D175 rearranges in the course of receptor desensitization. The overall results show that key residues at the ACh binding site differentially stabilize the agonist bound to closed, open and desensitized states, and provide a set point for gating of the channel.
通过定义先天性肌无力综合征(CMS)中的功能缺陷,我们发现位于乙酰胆碱受体(AChR)ε亚基结合位点区域的两个突变残基对ACh结合产生相反作用,并抑制通道门控。单通道动力学分析表明,第一个突变εN182Y增加了静息关闭状态下ACh对受体的亲和力,这促进了结合位点的顺序占据,并揭示了非突变αδ位点的ACh占据速率常数。对δ亚基中类似突变δN187Y的研究,揭示了非突变αε位点的ACh占据速率常数。第二个CMS突变εD175N降低了静息关闭状态下ACh对受体的亲和力;突变位点的占据仍促进门控,因为关闭和开放状态之间保持着很大的亲和力差异。然而,εD175N通过独立于ACh占据的效应损害整体门控。当映射到AChR结合位点的结构模型上时,εN182Y定位于与α亚基的界面,而εD175定位于ACh结合腔的入口。εN182Y和εD175在影响关闭状态相对于脱敏状态亲和力方面均表现出状态特异性,这表明携带εN182和εD175的蛋白质链在受体脱敏过程中发生了重排。总体结果表明,ACh结合位点的关键残基以不同方式稳定了与关闭、开放和脱敏状态结合的激动剂,并为通道门控提供了一个设定点。