A high-affinity recombinant antibody permits rapid and sensitive direct detection of myeloperoxidase

髓过氧化物酶 重组DNA 免疫分析 抗体 表面等离子共振 化学 分析物 噬菌体展示 计算生物学 色谱法 生物化学 生物 免疫学 纳米技术 材料科学 纳米颗粒 炎症 基因
作者
Barry J. McDonnell,Stephen Hearty,William J. J. Finlay,Richard O’Kennedy
出处
期刊:Analytical Biochemistry [Elsevier]
卷期号:410 (1): 1-6 被引量:24
标识
DOI:10.1016/j.ab.2010.09.039
摘要

Over the past 10 years, a growing field of research supporting the value of myeloperoxidase (MPO) as a prognostic indicator in acute cardiac pathophysiologies has emerged. The availability of a rapid and disposable MPO detection platform would enable research clinicians to more readily assess MPO indications for guiding therapy and also facilitate clinicians at the patient interface to readily adopt MPO testing and potentially drive more informed prognoses. Here we describe the isolation of a high-affinity avian MPO-specific recombinant antibody panel using phage display. Rapid isolation of a suitable single-chain variable fragment (scFv) antibody was facilitated using a surface plasmon resonance (SPR)-based “off-rate ranking” screening process. The selected scFv was then successfully incorporated into a rapid, simple, and sensitive one-step lateral flow immunoassay (LFIA) for the detection of MPO. This “one-step” feature of the developed assay was made possible by the scFv’s strong affinity for MPO, obviating the need for sandwich signal enhancement steps. The assay’s rapid performance was also further enhanced by exploiting the intrinsic enzymatic properties of MPO in its final detection. Use of the optimized LFIA facilitated the sensitive detection of MPO in MPO-depleted serum within clinically relevant reference ranges.

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