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可编程核酸纳米开关用于快速、一步检测体液中的抗体。

Programmable Nucleic Acid Nanoswitches for the Rapid, Single-Step Detection of Antibodies in Bodily Fluids.

机构信息

Department of Chemistry, University of Rome , Tor Vergata, Via della Ricerca Scientifica, 00133 Rome, Italy.

Ulisse BioMed S.r.l. , Area Science Park, 34149 Trieste, Italy.

出版信息

J Am Chem Soc. 2018 Jan 24;140(3):947-953. doi: 10.1021/jacs.7b09347. Epub 2018 Jan 9.

Abstract

Antibody detection plays a pivotal role in the diagnosis of pathogens and monitoring the success of vaccine immunization. However, current serology techniques require multiple, time-consuming washing and incubation steps, which limit their applicability in point-of-care (POC) diagnostics and high-throughput assays. We developed here a nucleic acid nanoswitch platform able to instantaneously measure immunoglobulins of type G and E (IgG and IgE) levels directly in blood serum and other bodily fluids. The system couples the advantages of target-binding induced colocalization and nucleic acid conformational-change nanoswitches. Due to the modular nature of the recognition platform, the method can potentially be applied to the detection of any antibody for which an antigen can be conjugated to a nucleic acid strand. In this work we show the sensitive, fast and cost-effective detection of four different antibodies and demonstrate the possible use of this approach for the monitoring of antibody levels in HIV+ patients immunized with AT20 therapeutic vaccine.

摘要

抗体检测在病原体诊断和疫苗免疫成功监测中起着关键作用。然而,目前的血清学技术需要多次耗时的洗涤和孵育步骤,限制了它们在即时检测(POC)诊断和高通量检测中的应用。我们在这里开发了一种核酸纳米开关平台,能够在血清和其他体液中直接快速检测免疫球蛋白 G 和 E(IgG 和 IgE)的水平。该系统结合了目标结合诱导共定位和核酸构象变化纳米开关的优势。由于识别平台的模块化性质,该方法可能适用于检测任何可以与核酸链偶联的抗原的抗体。在这项工作中,我们展示了对四种不同抗体的敏感、快速和具有成本效益的检测,并证明了该方法在监测接受 AT20 治疗性疫苗免疫的 HIV+患者的抗体水平方面的可能应用。

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