A novel magnetic ligand-based assay for the electrochemical determination of BRD4

IF 5.6 1区 化学 Q1 CHEMISTRY, ANALYTICAL Talanta Pub Date : 2024-07-19 DOI:10.1016/j.talanta.2024.126577
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Abstract

The first magnetic ligand-based electrochemical assay aimed at the determination of BRD4 was developed and validated. BRD4 is an epigenetic regulator of great interest in oncology in relation to its overexpression observed in the pathogenesis of several cancer diseases. BRD4 also represents a major target for the development of innovative treatments aimed at protein inhibition or degradation. Despite the relevance of BRD4 both for diagnostics and therapeutic purposes, current methodologies for its determination are limited to commercial ELISA kits. We present a novel magnetic ligand-based assay for the electrochemical determination of BRD4. The developed assay is based on the use of a small synthetic fragment of the natural protein ligand for BRD4 as receptor, thus exploiting the intrinsic biological protein-protein recognition mechanism. In addition, the assay features the use of magnetic beads as immobilization platforms and peroxidase-conjugated monoclonal anti-BRD4 antibody for the generation of the electrochemical signal. The ligand-based assay shows outstanding performance in terms of rapidity, with results achievable in less than 20 min, no matrix effect when applied to human plasma or cell lysate samples, and excellent specificity. The proposed method exhibits a limit of detection of 2.66 nM and a response range tunable as a function of the amount of immobilized receptor. The developed ligand-based assay was successfully applied to the accurate determination of BRD4 in untreated cell lysates, as proven by the ELISA reference method. The good performance of the proposed bioassay for determination of BRD4 showed potential application of this strategy in convenient point-of-care testing.

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基于磁性配体的新型电化学测定 BRD4 方法
我们开发并验证了首个旨在测定 BRD4 的磁性配体电化学测定法。BRD4是一种表观遗传调控因子,在多种癌症发病机制中被观察到过表达,因此在肿瘤学中备受关注。BRD4 也是开发抑制或降解蛋白质的创新疗法的主要目标。尽管 BRD4 与诊断和治疗都很相关,但目前测定它的方法仅限于商业 ELISA 试剂盒。我们介绍了一种基于磁性配体的新型测定法,用于电化学测定 BRD4。所开发的检测方法基于使用 BRD4 天然蛋白配体的一个小合成片段作为受体,从而利用了生物蛋白-蛋白之间的内在识别机制。此外,该检测方法还使用磁珠作为固定平台,并使用过氧化物酶结合的单克隆抗 BRD4 抗体来产生电化学信号。这种基于配体的检测方法在快速性方面表现出色,可在 20 分钟内得到结果,应用于人体血浆或细胞裂解物样本时无基质效应,而且特异性极佳。该方法的检测限为 2.66 nM,响应范围可随固定受体的数量而调整。所开发的基于配体的检测方法成功地应用于准确测定未经处理的细胞裂解物中的 BRD4,这一点已被 ELISA 参考方法所证实。所提议的生物检测法在测定 BRD4 方面的良好性能表明,这种策略有望应用于便捷的床旁检测。
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来源期刊
Talanta
Talanta 化学-分析化学
CiteScore
12.30
自引率
4.90%
发文量
861
审稿时长
29 days
期刊介绍: Talanta provides a forum for the publication of original research papers, short communications, and critical reviews in all branches of pure and applied analytical chemistry. Papers are evaluated based on established guidelines, including the fundamental nature of the study, scientific novelty, substantial improvement or advantage over existing technology or methods, and demonstrated analytical applicability. Original research papers on fundamental studies, and on novel sensor and instrumentation developments, are encouraged. Novel or improved applications in areas such as clinical and biological chemistry, environmental analysis, geochemistry, materials science and engineering, and analytical platforms for omics development are welcome. Analytical performance of methods should be determined, including interference and matrix effects, and methods should be validated by comparison with a standard method, or analysis of a certified reference material. Simple spiking recoveries may not be sufficient. The developed method should especially comprise information on selectivity, sensitivity, detection limits, accuracy, and reliability. However, applying official validation or robustness studies to a routine method or technique does not necessarily constitute novelty. Proper statistical treatment of the data should be provided. Relevant literature should be cited, including related publications by the authors, and authors should discuss how their proposed methodology compares with previously reported methods.
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