TY - JOUR
T1 - Lipid Corona Formation from Nanoparticle Interactions with Bilayers
AU - Olenick, Laura L.
AU - Troiano, Julianne M.
AU - Vartanian, Ariane
AU - Melby, Eric S.
AU - Mensch, Arielle C.
AU - Zhang, Leili
AU - Hong, Jiewei
AU - Mesele, Oluwaseun
AU - Qiu, Tian
AU - Bozich, Jared
AU - Lohse, Samuel
AU - Zhang, Xi
AU - Kuech, Thomas R.
AU - Millevolte, Augusto
AU - Gunsolus, Ian
AU - McGeachy, Alicia C.
AU - Doğangün, Merve
AU - Li, Tianzhe
AU - Hu, Dehong
AU - Walter, Stephanie R.
AU - Mohaimani, Aurash
AU - Schmoldt, Angela
AU - Torelli, Marco D.
AU - Hurley, Katherine R.
AU - Dalluge, Joe
AU - Chong, Gene
AU - Feng, Z. Vivian
AU - Haynes, Christy L.
AU - Hamers, Robert J.
AU - Pedersen, Joel A.
AU - Cui, Qiang
AU - Hernandez, Rigoberto
AU - Klaper, Rebecca
AU - Orr, Galya
AU - Murphy, Catherine J.
AU - Geiger, Franz M.
N1 - Publisher Copyright:
© 2018 Elsevier Inc.
PY - 2018/11/8
Y1 - 2018/11/8
N2 - Although mixing nanoparticles with certain biological molecules can result in coronas that afford some control over how engineered nanomaterials interact with living systems, corona formation mechanisms remain enigmatic. Here, we report results from experiments and computer simulations that provide concrete lines of evidence for spontaneous lipid corona formation without active mixing upon attachment to stationary and suspended lipid bilayer membranes. Experiments show that polycation-wrapped particles disrupt the tails of zwitterionic lipids, increase bilayer fluidity, and leave the membrane with reduced ζ potentials. Computer simulations suggest that the contact ion pairing between the lipid head groups and the polycations' ammonium groups leads to the formation of stable, albeit fragmented, lipid bilayer coronas. The mechanistic insight regarding lipid corona formation can be used to improve control over nano-bio interactions and to help understand why some nanomaterial-ligand combinations are detrimental to organisms but others are not. Engineered nanoparticles hold not only promise for technological innovation but also possible unforeseen risks for organisms upon inadvertent release into the environment. Here, mechanistic insight is provided regarding spontaneous lipid corona formation from nanomaterial-membrane interactions that can be used to improve control over nano-bio interactions and to help understand why some nanomaterial-ligand combinations are detrimental to organisms but others are not. We identify ion pairing between the lipid head groups and certain ligands coating nanoparticles having diameters below 10 nm as a necessary condition for the formation of fragmented lipid coronas that engender new properties (ζ potential, stickiness, and composition) departing from the original particle formulation. These insights help predict the impact that the increasingly widespread use of engineered nanomaterials has on their fate once they enter the food chain, which many of them may eventually do. Mechanisms of corona formation around nanomaterials remain enigmatic. Here, we provide evidence for spontaneous lipid corona formation that engenders new particle properties without the need for active mixing upon attachment to stationary and suspended lipid bilayer membranes. The mechanism of lipid corona formation can be used to improve control over nano-bio interactions and to help understand why some nanomaterial-ligand combinations are detrimental to organisms but others are not.
AB - Although mixing nanoparticles with certain biological molecules can result in coronas that afford some control over how engineered nanomaterials interact with living systems, corona formation mechanisms remain enigmatic. Here, we report results from experiments and computer simulations that provide concrete lines of evidence for spontaneous lipid corona formation without active mixing upon attachment to stationary and suspended lipid bilayer membranes. Experiments show that polycation-wrapped particles disrupt the tails of zwitterionic lipids, increase bilayer fluidity, and leave the membrane with reduced ζ potentials. Computer simulations suggest that the contact ion pairing between the lipid head groups and the polycations' ammonium groups leads to the formation of stable, albeit fragmented, lipid bilayer coronas. The mechanistic insight regarding lipid corona formation can be used to improve control over nano-bio interactions and to help understand why some nanomaterial-ligand combinations are detrimental to organisms but others are not. Engineered nanoparticles hold not only promise for technological innovation but also possible unforeseen risks for organisms upon inadvertent release into the environment. Here, mechanistic insight is provided regarding spontaneous lipid corona formation from nanomaterial-membrane interactions that can be used to improve control over nano-bio interactions and to help understand why some nanomaterial-ligand combinations are detrimental to organisms but others are not. We identify ion pairing between the lipid head groups and certain ligands coating nanoparticles having diameters below 10 nm as a necessary condition for the formation of fragmented lipid coronas that engender new properties (ζ potential, stickiness, and composition) departing from the original particle formulation. These insights help predict the impact that the increasingly widespread use of engineered nanomaterials has on their fate once they enter the food chain, which many of them may eventually do. Mechanisms of corona formation around nanomaterials remain enigmatic. Here, we provide evidence for spontaneous lipid corona formation that engenders new particle properties without the need for active mixing upon attachment to stationary and suspended lipid bilayer membranes. The mechanism of lipid corona formation can be used to improve control over nano-bio interactions and to help understand why some nanomaterial-ligand combinations are detrimental to organisms but others are not.
KW - SDG3: Good health and well-being
KW - mechanisms of nanoparticle-specific toxicology
KW - nano-bio interface
KW - sustainability
UR - http://www.scopus.com/inward/record.url?scp=85057201369&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85057201369&partnerID=8YFLogxK
U2 - 10.1016/j.chempr.2018.09.018
DO - 10.1016/j.chempr.2018.09.018
M3 - Article
AN - SCOPUS:85057201369
SN - 2451-9308
VL - 4
SP - 2709
EP - 2723
JO - Chem
JF - Chem
IS - 11
ER -