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Functional Fluorinated Modifications on a Polyelectrolyte Coated Polydimethylsiloxane Substrate for Fabricating Antibody Microarrays

机译:聚电解质涂层的聚二甲基硅氧烷基板上的功能性氟化修饰,用于制造抗体微阵列。

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Fluorinated compounds exhibit hydrophobic, nonstick, and self-cleaning properties, making them attractive for use as the coating material for biochips. In this study, we copolymerized the fluorinated compound 1H,1H,2H-perfluoro-1-decene (FD) with acrylic acid (AA) and bonded the resulting copolymer with protein G on the surface of polyelectrolyte coated polydimethylsiloxane (PDMS) to form a functional surface that captures antibodies. We demonstrated that the modified PDMS surface remained hydrophobic while becoming resistant to nonspecific protein binding. Thus, aqueous sample solutions formed the droplets (4 (mu)L) on the surface without spreading and drying during the sample printing. Contact angle measurements showed that this functionalized surface was as hydrophobic as the native PDMS with a virtually constant contact angle over seven days of the study under dried condition at 4 deg C. Spectroscopic measurements revealed that FD/AA copolymerization formed a homogeneous and highly dense multilayer (50 mg/mm~(2)) with a fluorine coverage of 35.4percent. Moreover, protein G was shown to covalently bind to AA molecules on the surface at a binding density of 0.24 (mu)g/mm~(2). We demonstrated that the fluorinated coating withstood nonspecific binding with extremely low background emission, leading to bioassays that, without the need of blocking agents, exhibited six times more sensitivity than PEG coatings. The fluorinated PDMS antibody microarrays were further applied to accurately determine the absolute concentration of ER(alpha) in MCF-7 cells. In conclusion, the unique properties of fluorinated compounds, such as withstanding wetting, nonspecific binding and contamination, make them an excellent coating material for use in sensitive and simple on-chip assays.
机译:氟化化合物具有疏水,不粘和自清洁的特性,使其成为生物芯片的涂层材料具有吸引力。在这项研究中,我们将氟化化合物1H,1H,2H-全氟-1-癸烯(FD)与丙烯酸(AA)共聚,然后将所得共聚物与蛋白G结合在聚电解质涂层的聚二甲基硅氧烷(PDMS)的表面上,形成捕获抗体的功能表面。我们证明,改性的PDMS表面保持疏水性,同时变得对非特异性蛋白结合具有抗性。因此,样品水溶液在样品印刷过程中在表面上形成液滴(4μL)而没有散布和干燥。接触角测量表明,该功能化表面与天然PDMS一样疏水,在4摄氏度的干燥条件下,经过7天的研究,其接触角几乎恒定。光谱测量表明,FD / AA共聚形成了均匀且高度致密的多层(50 mg / mm〜(2)),氟覆盖率为35.4%。此外,显示出蛋白G以0.24μg/ mm 2(2)的结合密度共价结合至表面上的AA分子。我们证明了氟化涂层能够抵御非特异性结合,具有极低的背景发射,从而导致生物测定的结果是,不需要封闭剂,其灵敏度是PEG涂层的六倍。氟化PDMS抗体微阵列进一步应用于准确确定MCF-7细胞中ERα的绝对浓度。总而言之,氟化化合物的独特性能,例如可承受润湿,非特异性结合和污染,使其成为用于灵敏且简单的片上分析的出色涂层材料。

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