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利用介电泳从人血浆中收集血清白蛋白聚集体纳米颗粒。

Collection of serum albumin aggregate nanoparticles from human plasma by dielectrophoresis.

机构信息

Cancer Early Detection Advanced Research Center, Knight Cancer Institute, Oregon Health and Science University, Portland, Oregon, USA.

Department of Biomedical Engineering, School of Medicine, Oregon Health and Science University, Portland, Oregon, USA.

出版信息

Electrophoresis. 2024 Oct;45(19-20):1748-1763. doi: 10.1002/elps.202400046. Epub 2024 Jul 30.

Abstract

Dielectrophoresis (DEP) is a fast and reliable nanoparticle recovery method that utilizes nonuniform electric fields to manipulate particles based on their material composition and size, enabling recovery of biologically-derived nanoparticles from plasma for diagnostic applications. When applying DEP to undiluted human plasma, collection of endogenous albumin proteins was observed at electric field gradients much lower than predicted by theory to collect molecular proteins. To understand this collection, nanoparticle tracking analysis of bovine serum albumin (BSA) dissolved in 0.5× phosphate-buffered saline was performed and showed that albumin spontaneously formed aggregate nanoparticles with a mean diameter of 237 nm. These aggregates experienced a dielectrophoretic force as a function of aggregate radius rather than the diameter of individual protein molecules which contributed to their collection. In high conductance buffer (6.8 mS/cm), DEP was able to move these aggregates into regions of high electric field gradient, and in lower conductance buffer (0.68 mS/cm), these aggregates could be moved into high or low gradient regions depending on the applied frequency. Disruption of BSA aggregates using a nonionic detergent significantly decreased the particle diameter, resulting in decreased dielectrophoretic collection of albumin which increased the collection consistency of particles of interest. These results provide techniques to manipulate albumin aggregates via DEP, which impacts collection of diagnostic biomarkers.

摘要

介电泳(DEP)是一种快速可靠的纳米颗粒回收方法,它利用非均匀电场根据颗粒的物质组成和大小来操纵颗粒,从而可以从等离子体中回收生物衍生的纳米颗粒,用于诊断应用。当将 DEP 应用于未稀释的人血浆时,观察到在比理论预测的要低得多的电场梯度下收集内源性白蛋白蛋白。为了理解这种收集,对溶解在 0.5×磷酸盐缓冲盐水中的牛血清白蛋白(BSA)进行了纳米颗粒跟踪分析,结果表明白蛋白自发形成平均直径为 237nm 的聚集体纳米颗粒。这些聚集体经历了作为聚集体半径而非单个蛋白质分子直径的函数的介电泳力,这有助于它们的收集。在高电导率缓冲液(6.8 mS/cm)中,DEP 能够将这些聚集体移动到高电场梯度区域,而在低电导率缓冲液(0.68 mS/cm)中,这些聚集体可以根据施加的频率移动到高或低梯度区域。使用非离子型洗涤剂破坏 BSA 聚集体会显著降低颗粒直径,从而减少白蛋白的介电泳收集,这增加了感兴趣颗粒的收集一致性。这些结果提供了通过 DEP 操纵白蛋白聚集体的技术,这会影响诊断生物标志物的收集。

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