TY - JOUR
T1 - Influence of single-stranded DNA Coatings on the Interaction between Graphene Nanoflakes and Lipid Bilayers
AU - Moore, Timothy C.
AU - Yang, Alexander H.
AU - Ogungbesan, Olu
AU - Hartkamp, Remco
AU - Iacovella, Christopher R.
AU - Zhang, Qi
AU - McCabe, Clare
N1 - Funding Information:
The manuscript was written through contributions of all authors. All authors have given approval to the final version of the manuscript. T.C.M., R.H., and C.R.I. performed and analyzed the free MD simulations of GNF insertion. A.H.Y. and O.O. performed and analyzed the steered MD simulations of GNF insertion. Q.Z. and C.McC. conceived and designed the study. This work was supported by National Science Foundation grant numbers CBET-1028374, DMR-1560414, and OAC-1835874 and by grant number R01 AR072679-01 from the National Institute of Arthritis and Musculoskeletal and Skin Diseases. Computational resources were provided by the National Energy Research Scientific Computing Center, supported by the Office of Science of the Department of Energy under Contract No. DE-AC02-05CH11231. The authors declare no competing financial interest.
Publisher Copyright:
© 2019 American Chemical Society.
PY - 2019/9/12
Y1 - 2019/9/12
N2 - Using molecular dynamics simulations, it is demonstrated that a partial coating of single-stranded DNA (ssDNA) reduces the penetration depth of a graphene nanoflake (GNF) into a phospholipid bilayer by attenuating the hydrophobic force that drives the penetration. As the GNF penetrates the bilayer, the ssDNA remains adsorbed to the GNF outside of the bilayer where it shields the graphene from the surrounding water. The penetration depth is found to be controlled by the amount of ssDNA coating the GNF, with a sparser coating resulting in a deeper penetration since the ssDNA shields less of the GNF surface. As the coating density is increased, the likelihood of the GNF entering the bilayer is reduced where it instead tends to lie flat on the bilayer surface with the sugar phosphate backbone of ssDNA interacting with the hydrophilic lipid head groups. While no bilayer disruption is observed for a partially inserted ssDNA-coated GNF, a larger, bare, partially inserted GNF is found to preferentially extract phospholipids from the bilayer, offering further evidence of lipid extraction as a main cytotoxicity mechanism of GNFs. Therefore, a coating of ssDNA may reduce the cytotoxicity of GNFs by shielding the unfavorable graphene-water interaction, thus preventing graphene penetration and lipid extraction.
AB - Using molecular dynamics simulations, it is demonstrated that a partial coating of single-stranded DNA (ssDNA) reduces the penetration depth of a graphene nanoflake (GNF) into a phospholipid bilayer by attenuating the hydrophobic force that drives the penetration. As the GNF penetrates the bilayer, the ssDNA remains adsorbed to the GNF outside of the bilayer where it shields the graphene from the surrounding water. The penetration depth is found to be controlled by the amount of ssDNA coating the GNF, with a sparser coating resulting in a deeper penetration since the ssDNA shields less of the GNF surface. As the coating density is increased, the likelihood of the GNF entering the bilayer is reduced where it instead tends to lie flat on the bilayer surface with the sugar phosphate backbone of ssDNA interacting with the hydrophilic lipid head groups. While no bilayer disruption is observed for a partially inserted ssDNA-coated GNF, a larger, bare, partially inserted GNF is found to preferentially extract phospholipids from the bilayer, offering further evidence of lipid extraction as a main cytotoxicity mechanism of GNFs. Therefore, a coating of ssDNA may reduce the cytotoxicity of GNFs by shielding the unfavorable graphene-water interaction, thus preventing graphene penetration and lipid extraction.
UR - http://www.scopus.com/inward/record.url?scp=85072134124&partnerID=8YFLogxK
U2 - 10.1021/acs.jpcb.9b04042
DO - 10.1021/acs.jpcb.9b04042
M3 - Article
C2 - 31405277
AN - SCOPUS:85072134124
SN - 1520-6106
VL - 123
SP - 7711
EP - 7721
JO - Journal of Physical Chemistry B
JF - Journal of Physical Chemistry B
IS - 36
ER -