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使用聚合物微柱阵列作为固相免疫测定的模板。

Use of Polymer Micropillar Arrays as Templates for Solid-Phase Immunoassays.

作者信息

Geissler Matthias, Ponton André, Nassif Christina, Malic Lidija, Turcotte Karine, Lukic Ljuboje, Morton Keith J, Veres Teodor

机构信息

Life Sciences Division, National Research Council of Canada, 75 de Mortagne Boulevard, Boucherville, QC J4B 6Y4, Canada.

出版信息

ACS Appl Polym Mater. 2022 May 2;4(8):5287-5297. doi: 10.1021/acsapm.2c00163. eCollection 2022 Aug 12.

Abstract

We investigate the use of periodic micropillar arrays produced by high-fidelity microfabrication with cyclic olefin polymers for solid-phase immunoassays. These three-dimensional (3D) templates offer higher surface-to-volume ratios than two-dimensional substrates, making it possible to attach more antibodies and so increase the signal obtained by the assay. Micropillar arrays also provide the capacity to induce wicking, which is used to distribute and confine antibodies on the surface with spatial control. Micropillar array substrates are modified by using oxygen plasma treatment, followed by grafting of (3-aminopropyl)triethoxysilane for binding proteins covalently using glutaraldehyde as a cross-linker. The relationship between microstructure and fluorescence signal was investigated through variation of pitch (10-50 μm), pillar diameter (5-40 μm), and pillar height (5-57 μm). Our findings suggest that signal intensity scales proportionally with the 3D surface area available for performing solid-phase immunoassays. A linear relationship between fluorescence intensity and microscale structure can be maintained even when the aspect ratio and pillar density both become very high, opening the possibility of tuning assay response by design such that desired signal intensity is obtained over a wide dynamic range compatible with different assays, analyte concentrations, and readout instruments. We demonstrate the versatility of the approach by performing the most common immunoassay formats-direct, indirect, and sandwich-in a qualitative fashion by using colorimetric and fluorescence-based detection for a number of clinically relevant protein markers, such as tumor necrosis factor alpha, interferon gamma (IFN-γ), and spike protein of severe acute respiratory syndrome coronavirus 2. We also show quantitative detection of IFN-γ in serum using a fluorescence-based sandwich immunoassay and calibrated samples with spike-in concentrations ranging from 50 pg/mL to 5 μg/mL, yielding an estimated limit of detection of ∼1 pg/mL for arrays with high micropillar density (11561 per mm) and aspect ratio (1:11.35).

摘要

我们研究了利用高保真微纳加工技术制备的周期性微柱阵列与环烯烃聚合物用于固相免疫分析。这些三维(3D)模板比二维基底具有更高的表面积与体积比,使得能够附着更多抗体,从而增加分析检测获得的信号。微柱阵列还具备引发毛细作用的能力,可用于在空间控制下将抗体分布并限制在表面。通过氧等离子体处理对微柱阵列基底进行改性,随后接枝(3-氨丙基)三乙氧基硅烷,以戊二醛作为交联剂共价结合蛋白质。通过改变间距(10 - 50μm)、柱直径(5 - 40μm)和柱高(5 - 57μm),研究了微观结构与荧光信号之间的关系。我们的研究结果表明,信号强度与可用于进行固相免疫分析的三维表面积成比例。即使纵横比和柱密度都变得非常高,荧光强度与微观结构之间仍可保持线性关系,这为通过设计调整分析检测响应开辟了可能性,从而在与不同分析方法、分析物浓度和读出仪器兼容的宽动态范围内获得所需的信号强度。我们通过使用比色法和基于荧光的检测方法,以定性方式对多种临床相关蛋白质标志物(如肿瘤坏死因子α、干扰素γ(IFN-γ)和严重急性呼吸综合征冠状病毒2的刺突蛋白)进行最常见的免疫分析形式(直接法、间接法和夹心法),展示了该方法的通用性。我们还使用基于荧光的夹心免疫分析法和浓度范围为50 pg/mL至5μg/mL的加标校准样品,对血清中的IFN-γ进行了定量检测,对于具有高微柱密度(每毫米11561个)和纵横比(1:11.35)的阵列,估计检测限约为1 pg/mL。

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