Hühn Jonas, Fedeli Chiara, Zhang Qian, Masood Atif, Del Pino Pablo, Khashab Niveen M, Papini Emanuele, Parak Wolfgang J
Fachbereich Physik, Philipps Universität Marburg, Marburg, Germany.
Department of Biomedical Science, University of Padova, Padova, Italy.
Int J Biochem Cell Biol. 2016 Jun;75:148-61. doi: 10.1016/j.biocel.2015.12.015. Epub 2015 Dec 31.
Protein adsorption to nanoparticles is described as a chemical reaction in which proteins attach to binding sites on the nanoparticle surface. This process is defined by a dissociation coefficient, which tells how many proteins are adsorbed per nanoparticle in dependence of the protein concentration. Different techniques to experimentally determine dissociation coefficients of protein adsorption to nanoparticles are reviewed. Results of more than 130 experiments in which dissociation coefficients have been determined are compared. Data show that different methods, nanoparticle systems, and proteins can lead to significantly different dissociation coefficients. However, we observed a clear tendency of smaller dissociation coefficients upon less negative towards more positive zeta potentials of the nanoparticles. The zeta potential thus is a key parameter influencing protein adsorption to the surface of nanoparticles. Our analysis highlights the importance of the characterization of the parameters governing protein-nanoparticle interaction for quantitative evaluation and objective literature comparison.
蛋白质在纳米颗粒上的吸附被描述为一种化学反应,其中蛋白质附着在纳米颗粒表面的结合位点上。这个过程由解离系数定义,该系数表明了每个纳米颗粒吸附的蛋白质数量如何依赖于蛋白质浓度。本文综述了实验测定蛋白质在纳米颗粒上吸附解离系数的不同技术。比较了130多个已测定解离系数的实验结果。数据表明,不同的方法、纳米颗粒系统和蛋白质会导致显著不同的解离系数。然而,我们观察到纳米颗粒的zeta电位从较负向更正变化时,解离系数有明显变小的趋势。因此,zeta电位是影响蛋白质在纳米颗粒表面吸附的关键参数。我们的分析强调了表征控制蛋白质-纳米颗粒相互作用的参数对于定量评估和客观文献比较的重要性。