基于免疫测定的检测肿瘤坏死因子-α的金纳米簇复合物的开发。

IF 1.6 4区 医学 Q4 BIOCHEMICAL RESEARCH METHODS
Natchanok Talapphet, Chang Soon Huh, Moon-Moo Kim
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引用次数: 0

摘要

肿瘤坏死因子-α(TNF-α)是一种细胞因子,被认为是炎症反应的关键调节因子,主要由活化的单核细胞和巨噬细胞产生。测量 TNF-α 的水平是追踪多种疾病和病理状态的重要指标。纳米金技术被认为是一种高效催化剂,具有测量炎症细胞因子的独特性能。本研究旨在合成金纳米团簇(AuNCs)和金纳米团簇-链霉亲和素系统,并研究其特性和球形形态。研究确定了用 AuNCs 检测 TNF-α 抗原的方法,并研究了一种新的基于 AuNCs 的免疫测定分析平台。研究表明,合成的 AuNCs 和 AuNCs-streptavidin 外观呈亮黄色,吸收峰分别在 A600 和 A610 纳米波长处。通过 TEM 分析可观察到其近似球形。AuNCs 对 TNF-α 抗原的检测灵敏度达到极限,线性剂量检测范围小于 1.25 ng/mL。在 Western 印迹分析中,条带大小和条带强度的乘积与 ~80 kDa、~55 kDa 和 ~25 kDa 范围内的 TNF-α 量成正比。用脂多糖(LPS)激活 RAW264.7 细胞后,用免疫测定法成功检测了细胞裂解物中的 TNF-α。这种检测方法速度快、灵敏度高、质量好,是检测 TNF-α 的可行替代方法,可确保其广泛应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development of gold nanocluster complex for the detection of tumor necrosis factor-alpha based on immunoassay

Tumor necrosis factor-alpha, TNF-α, a cytokine recognized as a key regulator of inflammatory responses, is primarily produced by activated monocytes and macrophages. Measuring TNF-α levels serves as a valuable indicator for tracking several diseases and pathological states. Gold nanotechnology has been identified as a highly effective catalyst with unique properties for measuring inflammatory cytokines. This study aimed to synthesize gold nanoclusters (AuNCs) and the AuNCs-streptavidin system, along with their characterizations and spherical morphology. The detection of TNF-α antigen with AuNCs was determined, and a new immunoassay-based AuNCs analytical platform was studied. In this study, it was demonstrated that the synthesized AuNCs and AuNCs-streptavidin showed a bright-yellow appearance with absorption peaks at A600 and A610 nm, respectively. The approximately spherical shape was observed by TEM analysis. The AuNCs demonstrated a sensitivity limit for the detection of the TNF-α antigen, with a linear dose-dependent detection range of less than 1.25 ng/mL. The products of the band sizes and band intensities were proportional to the amount of TNF-α in the range of ∼80 kDa, ∼55 kDa, and ∼ 25 kDa in western blot analysis. The TNF-α in cell lysate was successfully detected using an immunoassay after the activation of RAW264.7 cells with lipopolysaccharide (LPS). This assay may serve as a viable alternative for TNF-α detection with high speed, sensitivity, and qualities, ensuring its broad applications.

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来源期刊
CiteScore
4.10
自引率
0.00%
发文量
120
审稿时长
3 months
期刊介绍: The Journal of Immunological Methods is devoted to covering techniques for: (1) Quantitating and detecting antibodies and/or antigens. (2) Purifying immunoglobulins, lymphokines and other molecules of the immune system. (3) Isolating antigens and other substances important in immunological processes. (4) Labelling antigens and antibodies. (5) Localizing antigens and/or antibodies in tissues and cells. (6) Detecting, and fractionating immunocompetent cells. (7) Assaying for cellular immunity. (8) Documenting cell-cell interactions. (9) Initiating immunity and unresponsiveness. (10) Transplanting tissues. (11) Studying items closely related to immunity such as complement, reticuloendothelial system and others. (12) Molecular techniques for studying immune cells and their receptors. (13) Imaging of the immune system. (14) Methods for production or their fragments in eukaryotic and prokaryotic cells. In addition the journal will publish articles on novel methods for analysing the organization, structure and expression of genes for immunologically important molecules such as immunoglobulins, T cell receptors and accessory molecules involved in antigen recognition, processing and presentation. Submitted full length manuscripts should describe new methods of broad applicability to immunology and not simply the application of an established method to a particular substance - although papers describing such applications may be considered for publication as a short Technical Note. Review articles will also be published by the Journal of Immunological Methods. In general these manuscripts are by solicitation however anyone interested in submitting a review can contact the Reviews Editor and provide an outline of the proposed review.
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