| Literature DB >> 25794196 |
Sandra Ritz1, Susanne Schöttler1, Niklas Kotman1, Grit Baier1, Anna Musyanovych1, Jörg Kuharev2, Katharina Landfester1, Hansjörg Schild2, Olaf Jahn3, Stefan Tenzer2, Volker Mailänder1,4.
Abstract
Understanding nanoparticle-protein interactions is a crucial issue in the development of targeted nanomaterial delivery. Besides unraveling the composition of the nanoparticle's protein coronas, distinct proteins thereof could control nanoparticle uptake into specific cell types. Here we differentially analyzed the protein corona composition on four polymeric differently functionalized nanoparticles by label-free quantitative mass spectrometry. Next, we correlated the relative abundance of identified proteins in the corona with enhanced or decreased cellular uptake of nanoparticles into human cancer and bone marrow stem cells to identify key candidates. Finally, we verified these candidate proteins by artificially decorating nanoparticles with individual proteins showing that nanoparticles precoated with the apolipoproteins ApoA4 or ApoC3 significantly decreased the cellular uptake, whereas precoating with ApoH increased the cellular uptake.Entities:
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Year: 2015 PMID: 25794196 DOI: 10.1021/acs.biomac.5b00108
Source DB: PubMed Journal: Biomacromolecules ISSN: 1525-7797 Impact factor: 6.988