open access publication

Article, 2024

Differences in interaction of graphene/graphene oxide with bacterial and mammalian cell membranes

Nanoscale, ISSN 2040-3372, 2040-3364, Volume 16, 3, Pages 1156-1166, 10.1039/d3nr05354g

Contributors

Lanai, Victor [1] Chen, Yanyan [1] Naumovska, Elena 0000-0001-6011-5369 [1] Pandit, Santosh 0000-0002-8357-758X [1] Schröder, Elsebeth 0000-0003-4995-3585 [1] Mijakovic, Ivan 0000-0002-8860-6853 [1] [2] Rahimi, Shadi 0000-0002-8376-9880 [1]

Affiliations

  1. [1] Chalmers University of Technology
  2. [NORA names: Sweden; Europe, EU; Nordic; OECD];
  3. [2] Technical University of Denmark
  4. [NORA names: DTU Technical University of Denmark; University; Denmark; Europe, EU; Nordic; OECD]

Abstract

Graphene, a single layer, hexagonally packed two-dimensional carbon sheet is an attractive candidate for diverse applications including antibacterial potential and drug delivery. One of the knowledge gaps in biomedical application of graphene is the interaction of these materials with the cells. To address this, we investigated the interaction between graphene materials (graphene and graphene oxide) and plasma membranes of cells (bacterial and mammalian cells). The interactions of four of the most abundant phospholipids in bacteria and mammalian plasma membranes with graphene materials were studied using density functional theory (DFT) at the atomic level. The calculations showed that the mammalian phospholipids have stronger bonding to each other compared to bacterial phospholipids. When the graphene/graphene oxide sheet is approaching the phospholipid pairs, the bacterial pairs exhibit less repulsive interactions, thereby a more stable system with the sheets was found. We also assembled bacterial and mammalian phospholipids into liposomes. We further observed that the bacterial liposomes and cells let the graphene flakes penetrate the membrane. The differential scanning calorimetry measurements of liposomes revealed that the bacterial liposomes have the lowest heat capacity; this strengthens the theoretical predictions of weaker interaction between the bacterial phospholipids compared to the mammalian phospholipids. We further demonstrated that graphene oxide could be internalized into the mammalian liposomes without disrupting the membrane integrity. The results suggest that the weak bonding among bacteria phospholipids and less repulsive force when graphene materials approach, result in graphene materials interacting differently with the bacteria compared to mammalian cells.

Keywords

abundant phospholipid, applications, applications of graphene, approach, atomic level, bacteria, bacterial liposomes, bacterial pairs, bacterial phospholipids, biomedical applications, biomedical applications of graphene, bonds, calculations, capacity, carbon sheets, cell membrane, cells, delivery, density, density functional theory, differences, differential scanning calorimetry measurements, diverse applications, drug, drug delivery, flakes, force, functional theory, gap, graphene, graphene flakes, graphene materials, graphene oxide, graphene/graphene, graphene/graphene oxide, heat capacity, hexagon, integration, interaction, knowledge, knowledge gaps, levels, liposomes, low heat capacity, mammalian cell membranes, mammalian cells, mammalian phospholipids, mammalian plasma membranes, material approach, materials, measurements of liposomes, membrane, membrane integrity, membrane of cells, oxidation, oxide sheets, pairs, phospholipids, plasma, plasma membrane, plasma membrane of cells, prediction, repulsive force, repulsive interactions, results, sheet, stable system, strong bonding, system, theoretical predictions, theory, two-dimensional carbon sheets, weak bonds

Funders

  • Swedish Research Council
  • Novo Nordisk Foundation
  • Swedish Foundation for Strategic Research

Data Provider: Digital Science