绝缘体基微流体设备中的增强型绿色荧光蛋白流介电泳。

IF 3 3区 生物学 Q2 BIOCHEMICAL RESEARCH METHODS
Jerry Sheu, Sean Seyler, A K M Fazlul Karim Rasel, Mark A Hayes
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引用次数: 0

摘要

有诱人的证据表明,蛋白质可以在微流体设备中通过高阶电场效应进行精确和选择性操作。在这些平台上精确操纵蛋白质有望颠覆和革新许多领域,特别是分析生物化学领域。一些实验证据表明,与传统理论计算出的力相比,会产生更大的力,而这些更大的力来自蛋白质的微妙结构特征,从而提供了选择性。新理论在预测力的大小方面反映了一些实验证据,并包含了传统连续理论中缺乏的微妙结构特征。遗憾的是,实验证据大多是探索性的,缺乏一个或多个重要元素,不仅无法与其他现有数据进行清晰的解释和比较,也无法与不断发展的理论描述进行定量比较。本文介绍了一个清晰且可解释的实验系统,该系统可定量测定未标记、未聚集的原生结构蛋白质分子的介电泳感度,这些分子暴露在适度电场(105-106 V/m)中的时间很短(∼5 ms),但局部浓度不会显著增加。该平台使用亚纳克量的蛋白质,测定时的探测体积为几皮升,总分析时间为 10 秒。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Enhanced Green Fluorescent Protein Streaming Dielectrophoresis in Insulator-Based Microfluidic Devices.

There is tantalizing evidence that proteins can be accurately and selectively manipulated by higher order electric field effects within microfluidic devices. The accurate and precise manipulation of proteins in these platforms promises to disrupt and revolutionize many fields, most notably analytical biochemistry. Several lines of experimental evidence suggest much higher forces are generated compared to those calculated from traditional theories and those higher forces arise from subtle structural features of the proteins providing selectivity. New theories reflect some of the experimental evidence in the magnitude of the force predicted and inclusion of subtle structural features absent in traditional continuum theory. Unfortunately, the experimental evidence is largely exploratory in nature and lacks one or more important elements that prevents a clear interpretation and comparison to not only the other existing data, but also quantitative comparison to the evolving theoretical descriptions. Here, a clear and interpretable experimental system is presented that quantitatively determines the dielectrophoretic susceptibility of unlabeled, unaggregated native-structure protein molecules that are exposed to modest electric fields (105-106 V/m) for short periods of time (∼5 ms) without significant increases in local concentration. The platform uses sub-nanogram quantities of protein, the probed volume upon determination is a few picoliters, and the total analysis time is 10 s.

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来源期刊
ELECTROPHORESIS
ELECTROPHORESIS 生物-分析化学
CiteScore
6.30
自引率
13.80%
发文量
244
审稿时长
1.9 months
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.
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