Adsorption mechanism of an antimicrobial peptide on carbonaceous surfaces: a molecular dynamics study

Roccatano, Danilo, Sarukhanyan, Edita and Zangi, Ronen (2017) Adsorption mechanism of an antimicrobial peptide on carbonaceous surfaces: a molecular dynamics study. Journal of chemical Physics, 146 (7). 074703. ISSN 0021-9606

Full content URL:


Request a copy
26364 pdf_archiveJCPSA6vol_146iss_7074703_1_am (1).pdf
[img] PDF
ManuscriptRevision4_1_2017.pdf - Whole Document
Restricted to Repository staff only

26364 pdf_archiveJCPSA6vol_146iss_7074703_1_am (1).pdf - Whole Document

Item Type:Article
Item Status:Live Archive


Peptides are versatile molecules with applications spanning from biotechnology to nanomedicine. They exhibit a good capability to unbundle carbon nanotubes (CNT) by improving their solubility in water. Furthermore, they are a powerful drug delivery system since they can easily be uptaked by living cells, and their high surface to volume ratio facilitates the adsorption of molecules of different nature. Therefore, understanding the interaction mechanism between peptides and CNT is important for designing novel therapeutically agents. In this paper, the mechanisms of the adsorption of antimicrobial peptide Cecropin A – Magainin 2 (CA-MA) on a graphene nanosheet (GNS) and on an ultra-short single-walled CNT are characterized using molecular dynamics simulations. The results show that the peptide coats both GNS and CNT surfaces through preferential contacts with aromatic side chains. The peptide packs compactly on the carbon surfaces where the polar and functionalizable Lys side chains protrude into the bulk solvent. It is shown that the adsorption is strongly correlated to a loss of the peptide helical structure. In the case of the CNT, the outer surface is significantly more accessible for adsorption. Nevertheless when the outer surface is already covered by other peptides, a spontaneous diffusion, via the amidated C-terminus, into the interior of the CNT was observed within 150 ns of simulation time. We found that this spontaneous insertion into the CNT interior can be controlled by the polarity of the entrance rim. For the positively charged CA-MA peptide studied, hydrogenated and fluorinated rims, respectively, hinder and promote the insertion.

Keywords:Surphace coating, molecular dynamics, nanomaterials, graphene, carbon nanotube
Subjects:F Physical Sciences > F200 Materials Science
F Physical Sciences > F320 Chemical Physics
Divisions:College of Science > School of Mathematics and Physics
Related URLs:
ID Code:26364
Deposited On:15 Feb 2017 11:01

Repository Staff Only: item control page