The dynamics of PEG-coated nanoparticles in concentrated protein solutions up to the molecular crowding range

IF 13.9 Q1 CHEMISTRY, MULTIDISCIPLINARY Aggregate (Hoboken, N.J.) Pub Date : 2024-01-04 DOI:10.1002/agt2.483
Ferdinand Otto, Francesco Dallari, Fabian Westermeier, D. C. Florian Wieland, Wolfgang J. Parak, Felix Lehmkühler, Florian Schulz
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Abstract

Polymer-coated nanoparticles are widely studied in the context of nanomedicine and it is therefore of utmost importance to understand not only how their structure but also how their colloidal dynamics are affected by physiologically relevant conditions. A characteristic feature of the cytosol of cells is the very high concentration of proteins among other matrix components, often termed macromolecular crowding. Here, the structure and colloidal dynamics of poly(ethylene glycol) (PEG)-coated gold nanoparticles in the presence of bovine serum albumin (BSA) concentrations ranging from 0 to 265 mg/mL are studied with X-ray photon correlation spectroscopy. For protein–nanoparticle mixtures with high BSA concentrations, comparable to intracellular levels, a significant deviation of the apparent viscosity from expectations for pure BSA solutions is found. The findings strongly indicate that the nanoscopic viscous properties of the dense protein solutions are significantly affected by the nanoparticles. At these high concentrations, the colloidal stability of the samples depends on the molecular weight of the coating PEG–ligand, whereas at lower concentrations no differences are observed.

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PEG 涂层纳米粒子在浓缩蛋白质溶液中的动态变化,直至分子拥挤范围
聚合物包覆纳米粒子在纳米医学中被广泛研究,因此,了解其结构以及胶体动力学如何受到生理相关条件的影响至关重要。细胞胞体的一个特征是蛋白质与其他基质成分高度集中,这通常被称为大分子拥挤。本文利用 X 射线光子相关光谱法研究了聚乙二醇(PEG)包裹的金纳米粒子在牛血清白蛋白(BSA)浓度为 0 至 265 mg/mL 存在下的结构和胶体动力学。对于 BSA 浓度较高(与细胞内水平相当)的蛋白质-纳米粒子混合物,发现其表观粘度与纯 BSA 溶液的预期粘度有显著偏差。研究结果强烈表明,高密度蛋白质溶液的纳米粘度特性受到纳米粒子的显著影响。在这些高浓度条件下,样品的胶体稳定性取决于包覆 PEG 配体的分子量,而在低浓度条件下则观察不到差异。
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CiteScore
17.40
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审稿时长
7 weeks
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