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Protein denaturation caused by heat inactivation detrimentally affects biomolecular corona formation and cellular uptake

机译:蛋白质变性所引起的热失活有害地影响生物分子电晕形成和细胞吸收

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摘要

Adsorption of blood proteins to the surface of nanocarriers is known to be the critical factor influencing cellular interactions and eventually determining the successful application of nanocarriers as drug carriers in vivo. There is an increasing number of reports summarizing large data sets of all identified corona proteins. However, to date our knowledge about the multiple mechanisms mediating interactions between proteins and nanocarriers is still limited. In this study, we investigate the influence of protein structure on the adsorption process and focus on the effect of heat inactivation of serum and plasma, which is a common cell culture procedure used to inactivate the complement system. As in general routine lab procedure, heat inactivation was performed at 56 degrees C for 30 min in order to denature heat labile proteins. When nanocarriers were exposed to native versus heat inactivated serum, we saw that the cellular uptake by macrophages was significantly affected. These results were then correlated with an altered corona composition that depended on the treatment of the protein source. In summary, we were able to prove that the protein structure is one of the key parameters determining protein corona formation.
机译:吸附血液蛋白质的表面人们已知的关键因素影响细胞间的相互作用,最终确定的成功应用人们作为药物载体在体内。越来越多的报告总结数据集的确定电晕蛋白质。然而,到目前为止我们的知识多调解机制之间的相互作用蛋白质和人们仍然是有限的。这项研究中,我们调查的影响在吸附过程和蛋白质结构专注于热灭活血清的影响和等离子体,这是一种常见的细胞培养程序用于灭活补系统。在56摄氏度30失活了敏为了变性热不稳定的蛋白质。当人们受到本地和热灭活血清,我们看到的细胞被巨噬细胞吸收明显受到影响。这些结果都与一个改变电晕取决于组成治疗的蛋白质来源。能够证明蛋白质结构是什么确定蛋白质的一个关键参数电晕的形成。

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