TY  - JOUR
A1  - Oertel, Jana
A1  - Keller, Adrian
A1  - Prinz, Julia
A1  - Schreiber, Benjamin
A1  - Huebner, Rene
A1  - Kerbusch, Jochen
A1  - Bald, Ilko
A1  - Fahmy, Karim
T1  - Anisotropic metal growth on phospholipid nanodiscs via lipid bilayer expansion
JF  - Scientific reports
N2  - Self-assembling biomolecules provide attractive templates for the preparation of metallic nanostructures. However, the intuitive transfer of the "outer shape" of the assembled macromolecules to the final metallic particle depends on the intermolecular forces among the biomolecules which compete with interactions between template molecules and the metal during metallization. The shape of the bio-template may thus be more dynamic than generally assumed. Here, we have studied the metallization of phospholipid nanodiscs which are discoidal particles of similar to 10 nm diameter containing a lipid bilayer similar to 5 nm thick. Using negatively charged lipids, electrostatic adsorption of amine-coated Au nanoparticles was achieved and followed by electroless gold deposition. Whereas Au nanoparticle adsorption preserves the shape of the bio-template, metallization proceeds via invasion of Au into the hydrophobic core of the nanodisc. Thereby, the lipidic phase induces a lateral growth that increases the diameter but not the original thickness of the template. Infrared spectroscopy reveals lipid expansion and suggests the existence of internal gaps in the metallized nanodiscs, which is confirmed by surface-enhanced Raman scattering from the encapsulated lipids. Interference of metallic growth with non-covalent interactions can thus become itself a shape-determining factor in the metallization of particularly soft and structurally anisotropic biomaterials.
Y1  - 2016
U6  - https://doi.org/10.1038/srep26718
SN  - 2045-2322
VL  - 6
PB  - Nature Publ. Group
CY  - London
ER  - 
TY  - JOUR
A1  - Kretzschmar, Jerome
A1  - Haubitz, Toni
A1  - Huebner, Rene
A1  - Weiss, Stephan
A1  - Husar, Richard
A1  - Brendler, Vinzenz
A1  - Stumpf, Thorsten
T1  - Network-like arrangement of mixed-valence uranium oxide nanoparticles after glutathione-induced reduction of uranium(VI)
JF  - Chemical communications
N2  - Glutathione (GSH), a ubiquitous intracellular reducing tripeptide, is able to reduce hexavalent uranium, U(VI), to its tetravalent form, U(IV), in aqueous media in vitro, inducing the formation of nanocrystalline mixed-valence uranium oxide particles. After the initial reduction to U(V) and subsequent dismutation, the yielded U(IV) rapidly hydrolyses under near-neutral conditions forming 2-5 nm sized nanoparticles. The latter further aggregate to 20-40 nm chain-like building blocks that finally arrange as network-like structures.
Y1  - 2018
U6  - https://doi.org/10.1039/c8cc02070a
SN  - 1359-7345
SN  - 1364-548X
VL  - 54
IS  - 63
SP  - 8697
EP  - 8700
PB  - Royal Society of Chemistry
CY  - Cambridge
ER  -