Designing new surfactant peptides for binding to carbon nanotubes via computational approaches

作者：Mansouri Alireza; Mahnam Karim^*

来源：Journal of Molecular Graphics and Modelling, 2017, 74: 61-72.

DOI：10.1016/j.jmgm.2017.02.016

• Carbon nanotubes
• Surfactant peptide
• Molecular dynamics simulation
• Steric hindrance
• Docking
• MM-PBSA binding free energy

The non-covalent interaction between single-walled carbon nanotube and surfactant peptides makes them soluble in biological media to be used in nano-medicine, drug delivery and gene therapy. Pervious study has shown that two important parameters in binding peptides into nanotubes are hydrophobic effect and the number of aromatic amino acids. Ten surfactant peptides with the length of eight residue, including Lys, Trp, Tyr, Phe and Val, were designed to investigate the important parameters in binding peptides to a (6, 6) carbon nanotube. 500 ns MD simulation was performed for free surfactant peptides in water or near to a nanotube. Our results have indicated that the binding affinity of peptides to nanotube increases with the increase of aromatic residue content. Also, among aromatic residues, the peptides containingTrp residues have higher binding affinity to nanotube compared to the peptides with Phe or Tyr residue. Steric hindrance between bulky aromatic residues in peptide sequence has negative influence in binding peptide to nanotube, and in designing a surfactant peptide, the number and distance of aromatic residue and polarity of them should be taken into account. Our results also show that in docking peptides to nanotube, full-flexible docking leads to incorrect results.

• 出版日期2017-6