Ritz Sandra, Schöttler Susanne, Kotman Niklas, Baier Grit, Musyanovych Anna, Kuharev Jörg, Landfester Katharina, Schild Hansjörg, Jahn Olaf, Tenzer Stefan, Mailänder Volker
†Max Planck Institute for Polymer Research, Ackermannweg 10, 55128 Mainz, Germany.
§Institute for Immunology, University Medical Center of Mainz, Langenbeckstr.1, 55101 Mainz, Germany.
Biomacromolecules. 2015 Apr 13;16(4):1311-21. doi: 10.1021/acs.biomac.5b00108. Epub 2015 Apr 3.
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.
了解纳米颗粒与蛋白质的相互作用是靶向纳米材料递送发展中的一个关键问题。除了解析纳米颗粒蛋白质冠层的组成外,其中不同的蛋白质还可以控制纳米颗粒被特定细胞类型摄取。在此,我们通过无标记定量质谱法对四种不同功能化的聚合物纳米颗粒上的蛋白质冠层组成进行了差异分析。接下来,我们将冠层中已鉴定蛋白质的相对丰度与纳米颗粒在人类癌细胞和骨髓干细胞中增强或降低的细胞摄取相关联,以确定关键候选蛋白。最后,我们通过用单个蛋白质人工修饰纳米颗粒来验证这些候选蛋白,结果表明,预先包被载脂蛋白ApoA4或ApoC3的纳米颗粒显著降低了细胞摄取,而预先包被ApoH则增加了细胞摄取。