Different effects of cholesterol on membrane permeation of arginine and tryptophan revealed by bias-exchange metadynamics simulations

作者：Cao, Zanxia; Zhang, Xiumei; Wang, Chunling; Liu, Lei; Zhao, Liling; Wang, Jihua^*; Zhou, Yaoqi^*

来源：Journal of Chemical Physics, 2019, 150(8): 084106.

DOI：10.1063/1.5082351

• MOLECULAR-DYNAMICS SIMULATIONS
• HIV-1 TAT PEPTIDE
• FREE-ENERGY
• CELLULAR UPTAKE
• LIPID-BILAYER
• AMINO-ACIDS
• FORCE-FIELD
• TRANSLOCATION
• DIPALMITOYLPHOSPHATIDYLCHOLINE
• PERMEABILITY

Experiments have shown that cholesterol influences the membrane permeability of small molecules, amino acids, and cell-penetrating peptides. However, their exact translocation mechanisms under the influence of cholesterol remain poorly understood. Given the practical importance of cell-penetrating peptides and the existence of varied cholesterol contents in different cell types, it is necessary to examine the permeation of amino acids in cholesterol-containing membranes at atomic level of details. Here, bias-exchange metadynamics simulations were employed to investigate the molecular mechanism of the membrane permeation of two amino acids Arg and Trp important for cell-penetrating peptides in the presence of different concentrations of cholesterol. We found that the free energy barrier of Arg+ (the protonated form) permeation increased linearly as the cholesterol concentration increased, whereas the barrier of Trp permeation had a rapid increase from 0 mol.% to 20 mol.% cholesterol-containing membranes and nearly unchanged from 20 mol.% to 40 mol.% cholesterol-containing membranes. Arg0 becomes slightly more stable than Arg+ at the center of the dipalmitoylphosphatidylcholine (DPPC) membrane with 40 mol.% cholesterol concentrations. As a result, Arg+ has a similar permeability as Trp at 0 mol.% and 20 mol.% cholesterol, but a significantly lower permeability than Trp at 40 mol.% cholesterol. This difference is caused by the gradual reduction of water defects for Arg+ as the cholesterol concentration increases but lack of water defects for Trp in cholesterol-containing membranes. Strong but different orientation dependence between Arg+ and Trp permeations is observed. These results provide an improved microscopic understanding of amino-acid permeation through cholesterol-containing DPPC membrane systems.

• 出版日期2019-2-28
• 单位德州学院