Rashid Md Harunur
School of Engineering, RMIT University, Melbourne, Victoria, 3001, Australia.
Department of Mathematics and Physics, North South University, Bashundhara, Dhaka, 1229, Bangladesh.
Biochem Biophys Rep. 2020 Dec 16;25:100879. doi: 10.1016/j.bbrep.2020.100879. eCollection 2021 Mar.
Mutations in the voltage-gated potassium channel Kv7.4 (encoded as KCNQ4) lead to the early onset of non-syndromic hearing loss, which is significant during language acquisition. The deletion of the S269 pore residue (genetic Δ mutation) in Kv7.4 has been reported to be associated with hearing loss. So far, there is no mechanistic understanding of how this mutation modulates channel function. To understand the role of S269 in ion conduction, we performed molecular dynamics simulations for both wild type and ΔS269 mutant channels. Simulations indicate that the ΔS269 mutation suppresses the fluctuations in the neighboring Y269 residue and thereby consolidates the ring formed by I307 and F310 residues in the adjacent S6 helixes in the cavity region. We show that the long side chains of I307 near the entrance to the cavity form a hydrophobic gate. Comparison of the free energy profiles of a cavity ion in Kv7.4 and Kv7.4[ΔS269] channels reveals a sizable energy barrier in the latter case, which suppresses ion conduction. Thus the simulation studies reveal that the hydrophobic gate resulting from the ΔS269 mutation appears to be responsible for sensorineural hearing loss.
电压门控钾通道Kv7.4(编码为KCNQ4)的突变会导致非综合征性听力损失的早期发作,这在语言习得过程中很明显。据报道,Kv7.4中S269孔残基的缺失(基因Δ突变)与听力损失有关。到目前为止,对于这种突变如何调节通道功能尚无机制上的了解。为了了解S269在离子传导中的作用,我们对野生型和ΔS269突变体通道进行了分子动力学模拟。模拟表明,ΔS269突变抑制了相邻Y269残基的波动,从而巩固了由腔区域相邻S6螺旋中的I307和F310残基形成的环。我们表明,靠近腔入口的I307的长侧链形成了一个疏水门。Kv7.4和Kv7.4[ΔS269]通道中腔离子的自由能分布比较显示,在后一种情况下存在相当大的能垒,这抑制了离子传导。因此,模拟研究表明,由ΔS269突变产生的疏水门似乎是感音神经性听力损失的原因。