TY - JOUR
T1 - Nanoparticles Interacting with Proteins and Cells
T2 - A Systematic Study of Protein Surface Charge Effects
AU - Shang, Li
AU - Yang, Linxiao
AU - Seiter, Jürgen
AU - Heinle, Marita
AU - Brenner-Weiss, Gerald
AU - Gerthsen, Dagmar
AU - Nienhaus, G. Ulrich
N1 - Publisher Copyright:
© 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
PY - 2014/4/1
Y1 - 2014/4/1
N2 - Despite intense research on biological and biomedical applications of nanoparticles, our understanding of their basic interactions with the biological environment is still incomplete. Systematic variation of the physicochemical properties of the nanoparticles is widely seen as a promising strategy to obtain further insights. In view of the key role of the protein adsorption layer forming on nanoparticles in contact with biofluids, we systematically varied the surface charge of proteins adsorbing onto nanoparticles by chemical modification so as to examine the effect of Coulomb forces in modulating nano-bio interactions. We chose human serum albumin (HSA) as a model protein and ultra-small, negatively charged fluorescent gold nanoclusters (AuNCs) as model nanoparticles. By using fluorescence and CD spectroscopies, we measured binding affinities and structural changes upon binding of the HSA variants. The strengths of the protein-nanoparticle interactions were found to change substantially upon modifying the surface charge of HSA. Furthermore, by using inductively coupled plasma optical emission spectroscopy, confocal fluorescence microscopy, scanning transmission electron microscopy and cell viability assays, we observed that cellular interactions of the AuNCs, including their adherence to cell membranes, uptake efficiency and cytotoxicity, depended markedly on the different surface charges of the HSA variants adsorbed onto the nanoparticles. These results illustrate vividly that the cellular responses to nanoparticle exposure depend on the specific properties of the proteins that adsorb onto nanoparticles from biofluids.
AB - Despite intense research on biological and biomedical applications of nanoparticles, our understanding of their basic interactions with the biological environment is still incomplete. Systematic variation of the physicochemical properties of the nanoparticles is widely seen as a promising strategy to obtain further insights. In view of the key role of the protein adsorption layer forming on nanoparticles in contact with biofluids, we systematically varied the surface charge of proteins adsorbing onto nanoparticles by chemical modification so as to examine the effect of Coulomb forces in modulating nano-bio interactions. We chose human serum albumin (HSA) as a model protein and ultra-small, negatively charged fluorescent gold nanoclusters (AuNCs) as model nanoparticles. By using fluorescence and CD spectroscopies, we measured binding affinities and structural changes upon binding of the HSA variants. The strengths of the protein-nanoparticle interactions were found to change substantially upon modifying the surface charge of HSA. Furthermore, by using inductively coupled plasma optical emission spectroscopy, confocal fluorescence microscopy, scanning transmission electron microscopy and cell viability assays, we observed that cellular interactions of the AuNCs, including their adherence to cell membranes, uptake efficiency and cytotoxicity, depended markedly on the different surface charges of the HSA variants adsorbed onto the nanoparticles. These results illustrate vividly that the cellular responses to nanoparticle exposure depend on the specific properties of the proteins that adsorb onto nanoparticles from biofluids.
KW - cellular uptake
KW - charge effects
KW - gold nanoclusters
KW - nano-bio interactions
UR - http://www.scopus.com/inward/record.url?scp=84893450129&partnerID=8YFLogxK
U2 - 10.1002/admi.201300079
DO - 10.1002/admi.201300079
M3 - 文章
AN - SCOPUS:84893450129
SN - 2196-7350
VL - 1
JO - Advanced Materials Interfaces
JF - Advanced Materials Interfaces
IS - 2
M1 - 1300079
ER -