| Literature DB >> 27606563 |
Haixia Wang1, Li Shang1,2,3, Pauline Maffre1, Siegfried Hohmann4, Frank Kirschhöfer4, Gerald Brenner-Weiß4, Gerd Ulrich Nienhaus1,2,5,6.
Abstract
Biological responses of cells and organisms to nanoparticle exposure crucially depend on the properties of the protein adsorption layer ("protein corona") forming on nanoparticle surfaces and their characterization is a crucial step toward a deep, mechanistic understanding of their build-up. Previously, adsorption of one type of model protein on nanoparticles was systematically studied in situ by using fluorescence correlation spectroscopy. Here, the first such study of interactions is presented between water-solubilized CdSe/ZnS quantum dots (QDs) and a complex biofluid, human blood serum. Despite the large number of proteins in serum, a protein layer of well-defined (average) thickness forming on QD surfaces is observed. Both the thickness and the apparent binding affinity depend on the type of QD surface ligand. Kinetic experiments reveal that the protein corona formed from serum is irreversibly bound, whereas the one formed from human serum albumin was earlier observed to be reversible. By using sodium dodecyl sulfate-polyacrylamide gel electrophoresis and mass spectrometry, the most abundant serum proteins contributing to the formation of a hard corona on the QDs are identified.Entities:
Keywords: fluorescence correlation spectroscopy; protein adsorption; protein corona; quantum dots; serum; surface effects
Year: 2016 PMID: 27606563 DOI: 10.1002/smll.201602283
Source DB: PubMed Journal: Small ISSN: 1613-6810 Impact factor: 13.281