Department of Energy Science & Engineering, Daegu Gyeongbuk Institute of Science & Technology (DGIST), Daegu 42988, Korea.
Energy Science & Engineering Research Center, Daegu Gyeongbuk Institute of Science & Technology (DGIST), Daegu 42988, Korea.
J Phys Chem B. 2024 Nov 7;128(44):10894-10903. doi: 10.1021/acs.jpcb.4c04266. Epub 2024 Oct 24.
It is well-known that membrane deformation and water pores contribute to the spontaneous translocation of arginine-rich cell-penetrating peptides (CPPs). We confirm this through the observation of the spontaneous translocation of single R9 (nona-arginine) and Tat (48-60) peptides across a model membrane using the weighted ensemble (WE) method within all-atom molecular dynamics (MD) simulations. Furthermore, we demonstrate that membrane deformation and the presence of a water pore reduce the effective charge of the CPP and the bending rigidity of the model membrane during translocation. We find that R9 disturbs the model membrane more than Tat (48-60), leading to more efficient translocation of R9 across the model membrane.
众所周知,膜变形和水孔有助于富含精氨酸的细胞穿透肽(CPPs)的自发转运。我们通过使用加权集合(WE)方法在全原子分子动力学(MD)模拟中观察到单个 R9(九聚精氨酸)和 Tat(48-60)肽穿过模型膜的自发转运,从而证实了这一点。此外,我们证明膜变形和水孔的存在会降低 CPP 的有效电荷和模型膜在转运过程中的弯曲刚度。我们发现 R9 比 Tat(48-60)更能扰乱模型膜,从而导致 R9 更有效地穿过模型膜进行转运。