Nishizawa Kazuhisa, Nishizawa Manami, Gnanasambandam Radhakrishnan, Sachs Frederick, Sukharev Sergei I, Suchyna Thomas M
Teikyo University School of Medical Technology, Tokyo, Japan.
Teikyo University School of Medical Technology, Tokyo, Japan.
Biochim Biophys Acta. 2015 Nov;1848(11 Pt A):2767-78. doi: 10.1016/j.bbamem.2015.09.003. Epub 2015 Sep 2.
GsMTx4, a gating modifier peptide acting on cationic mechanosensitive channels, has a positive charge (+5e) due to six Lys residues. The peptide does not have a stereospecific binding site on the channel but acts from the boundary lipids within a Debye length of the pore probably by changing local stress. To gain insight into how these Lys residues interact with membranes, we performed molecular dynamics simulations of Lys to Glu mutants in parallel with our experimental work. In silico, K15E had higher affinity for 1-palmitoyl-2-oleoyl-glycero-3-phosphocholine bilayers than wild-type (WT) peptide or any other mutant tested, and showed deeper penetration than WT, a finding consistent with the experimental data. Experimentally, the inhibitory activities of K15E and K25E were most compromised, whereas K8E and K28E inhibitory activities remained similar to WT peptide. Binding of WT in an interfacial mode did not influence membrane thickness. With interfacial binding, the direction of the dipole moments of K15E and K25E was predicted to differ from WT, whereas those of K8E and K28E oriented similarly to that of WT. These results support a model in which binding of GsMTx4 to the membrane acts like an immersible wedge that serves as a membrane expansion buffer reducing local stress and thus inhibiting channel activity. In simulations, membrane-bound WT attracted other WT peptides to form aggregates. This may account for the positive cooperativity observed in the ion channel experiments. The Lys residues seem to fine-tune the depth of membrane binding, the tilt angle, and the dipole moments.
GsMTx4是一种作用于阳离子机械敏感通道的门控修饰肽,由于含有六个赖氨酸残基而带正电荷(+5e)。该肽在通道上没有立体特异性结合位点,而是可能通过改变局部应力,从孔道德拜长度内的边界脂质起作用。为了深入了解这些赖氨酸残基如何与膜相互作用,我们在开展实验工作的同时,对赖氨酸到谷氨酸的突变体进行了分子动力学模拟。在计算机模拟中,K15E对1-棕榈酰-2-油酰甘油-3-磷酸胆碱双层膜的亲和力高于野生型(WT)肽或任何其他测试的突变体,并且比WT表现出更深的渗透,这一发现与实验数据一致。在实验中,K15E和K25E的抑制活性受到的影响最大,而K8E和K28E的抑制活性与WT肽相似。WT以界面模式结合不会影响膜厚度。通过界面结合,预测K15E和K25E的偶极矩方向与WT不同,而K8E和K28E的偶极矩方向与WT相似。这些结果支持了一个模型,即GsMTx4与膜的结合就像一个可浸入的楔子,作为膜扩张缓冲剂,减少局部应力,从而抑制通道活性。在模拟中,膜结合的WT吸引其他WT肽形成聚集体。这可能解释了在离子通道实验中观察到的正协同性。赖氨酸残基似乎对膜结合深度、倾斜角度和偶极矩进行了微调。