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生物纳米界面的竞争:一种蛋白质、一种多糖和一种脂肪酸吸附到磁性纳米颗粒上。

Competition at the Bio-nano Interface: A Protein, a Polysaccharide, and a Fatty Acid Adsorb onto Magnetic Nanoparticles.

作者信息

Abarca-Cabrera Lucía, Xu Lianxin, Berensmeier Sonja, Fraga-García Paula

机构信息

Bioseparation Engineering Group, Department of Energy and Process Engineering, TUM School of Engineering and Design, Technical University of Munich, Garching 85748, Germany.

出版信息

ACS Appl Bio Mater. 2023 Jan 16;6(1):146-156. doi: 10.1021/acsabm.2c00812. Epub 2022 Dec 12.

Abstract

Magnetic nanoparticles are an attractive bioseparation tool due to their magnetic susceptibility and high adsorption capacity for different types of molecules. A major challenge for separation is to generate selectivity for a target molecule, or for a group of molecules in complex environments such as cell lysates. It is crucial to understand the factors that determine the targets' adsorption behavior in mixtures for triggering intended interactions and selectivity. Here we use a model system containing three molecules, each of them a common representative of the more abundant types of macromolecules in living systems: sodium oleate (SO), a fatty acid; bovine serum albumin (BSA), a protein; and dextran, a polysaccharide. Our results show that (a) the BSA adsorption capacity on the iron oxide material depends markedly on the pH, with the maximum capacity at the pI of the protein (0.39 g g ); (b) sodium oleate, a strongly negatively charged molecule, an organic anion, renders a maximum adsorption capacity of 0.40 g g, even at pHs at which oleate as well as the nanoparticle surface are negatively charged; (c) the adsorbed masses of dextran, a neutral sugar, are lower than for the other two molecules, between 0.09 and 0.13 g g, regardless of the system's pH. We observe an unexpected behavior in mixtures: SO completely prevents the adsorption of BSA, and dextran decreases the adsorption of the other competitors, SO and BSA, while adsorbing at the same capacities, unaffected by either the presence of the other two molecules or the pH. BSA does not decrease the oleate adsorption capacity. We demonstrate the essential role of pH in the adsorption of BSA (a protein) and SO (a fatty acid), as well as its impact in the structural organization of the oleate molecules in water. Moreover, we present exciting data on the adsorption of the molecules in competition, revealing the need to focus on interaction studies in more complex environments. This study attempts to open the scope of the current research of bio-nano interactions to not only proteins but also to mixtures, and generally to molecules with other physicochemical characteristics. Furthermore, we contribute to the understanding of multicomponent systems with the vision set in enhancing biomass exploitation and biofractionation processes.

摘要

磁性纳米颗粒因其磁化率和对不同类型分子的高吸附能力而成为一种有吸引力的生物分离工具。分离面临的一个主要挑战是在复杂环境(如细胞裂解液)中对目标分子或一组分子产生选择性。了解在混合物中决定目标分子吸附行为的因素对于引发预期的相互作用和选择性至关重要。在这里,我们使用一个包含三种分子的模型系统,每种分子都是生命系统中更丰富类型的大分子的常见代表:油酸钠(SO),一种脂肪酸;牛血清白蛋白(BSA),一种蛋白质;以及葡聚糖,一种多糖。我们的结果表明:(a)BSA在氧化铁材料上的吸附容量明显取决于pH值,在蛋白质的等电点(pI)时达到最大容量(0.39 g/g);(b)油酸钠,一种带强负电荷的分子,一种有机阴离子,即使在油酸根以及纳米颗粒表面都带负电荷的pH值下,其最大吸附容量仍为0.40 g/g;(c)葡聚糖,一种中性糖,其吸附质量低于其他两种分子,在0.09至0.13 g/g之间,与系统的pH值无关。我们在混合物中观察到一种意想不到的行为:SO完全阻止BSA的吸附,而葡聚糖降低其他竞争者(SO和BSA)的吸附能力,同时以相同的容量吸附,不受其他两种分子的存在或pH值的影响。BSA不会降低油酸根的吸附容量。我们证明了pH值在BSA(一种蛋白质)和SO(一种脂肪酸)吸附中的重要作用,以及它对水中油酸根分子结构组织的影响。此外,我们展示了关于竞争分子吸附的令人兴奋的数据,揭示了在更复杂环境中关注相互作用研究的必要性。本研究试图拓宽当前生物纳米相互作用研究的范围,不仅包括蛋白质,还包括混合物,以及一般具有其他物理化学特性的分子。此外,我们以增强生物质利用和生物分馏过程为目标,有助于对多组分系统的理解。

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