Jason Ware, Delaney Shea, Jeong Youn Lim, Anna Malakian, Randall Armstrong, Ronald Pethig, Stuart Ibsen
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引用次数: 0
摘要
介电泳(DEP)是一种快速可靠的纳米粒子回收方法,它利用非均匀电场,根据粒子的材料成分和大小对粒子进行处理,从而从血浆中回收生物纳米粒子,用于诊断应用。将 DEP 应用于未稀释的人体血浆时,在电场梯度比理论预测的分子蛋白质收集梯度低得多的情况下,观察到了内源性白蛋白的收集。为了了解这种收集情况,对溶解在 0.5× 磷酸盐缓冲盐水中的牛血清白蛋白(BSA)进行了纳米粒子跟踪分析,结果表明白蛋白自发形成了平均直径为 237 纳米的聚集纳米粒子。这些聚集体产生的介电泳力是聚集体半径的函数,而不是单个蛋白质分子直径的函数,这有助于它们的聚集。在高电导缓冲液(6.8 mS/cm)中,DEP 能够将这些聚集体移动到高电场梯度区域,而在低电导缓冲液(0.68 mS/cm)中,根据应用频率的不同,这些聚集体可被移动到高梯度或低梯度区域。使用非离子洗涤剂破坏 BSA 聚集体可显著降低颗粒直径,从而减少白蛋白的介电泳收集,提高相关颗粒的收集一致性。这些结果提供了通过 DEP 处理白蛋白聚集体的技术,从而影响了诊断生物标记物的收集。
Collection of serum albumin aggregate nanoparticles from human plasma by dielectrophoresis
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.
期刊介绍:
ELECTROPHORESIS is an international journal that publishes original manuscripts on all aspects of electrophoresis, and liquid phase separations (e.g., HPLC, micro- and nano-LC, UHPLC, micro- and nano-fluidics, liquid-phase micro-extractions, etc.).
Topics include new or improved analytical and preparative methods, sample preparation, development of theory, and innovative applications of electrophoretic and liquid phase separations methods in the study of nucleic acids, proteins, carbohydrates natural products, pharmaceuticals, food analysis, environmental species and other compounds of importance to the life sciences.
Papers in the areas of microfluidics and proteomics, which are not limited to electrophoresis-based methods, will also be accepted for publication. Contributions focused on hyphenated and omics techniques are also of interest. Proteomics is within the scope, if related to its fundamentals and new technical approaches. Proteomics applications are only considered in particular cases.
Papers describing the application of standard electrophoretic methods will not be considered.
Papers on nanoanalysis intended for publication in ELECTROPHORESIS should focus on one or more of the following topics:
• Nanoscale electrokinetics and phenomena related to electric double layer and/or confinement in nano-sized geometry
• Single cell and subcellular analysis
• Nanosensors and ultrasensitive detection aspects (e.g., involving quantum dots, "nanoelectrodes" or nanospray MS)
• Nanoscale/nanopore DNA sequencing (next generation sequencing)
• Micro- and nanoscale sample preparation
• Nanoparticles and cells analyses by dielectrophoresis
• Separation-based analysis using nanoparticles, nanotubes and nanowires.