即插即用抗原检测的快速模块化纳米体检测。

IF 3.9 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
N. Rebecca Kang, Jisoo Im, John R. Biondo, Caitlin E. Sharpes, Katherine A. Rhea, Padric M. Garden, Juan J. Jaramillo Montezco, Alina Ringaci, Mark W. Grinstaff, Daniel A. Phillips, Aleksandr E. Miklos and Alexander A. Green*, 
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引用次数: 0

摘要

快速和便携的抗原检测对于管理传染病和应对有毒物质暴露至关重要,但目前的方法面临重大限制。像酶联免疫吸附试验(ELISA)这样的高灵敏度平台对于定点检测来说时间和成本都太高,而像横向流动试验(LFAs)这样的便携式选择需要对新靶点进行系统的检查。此外,复杂的基础设施、高生产成本和检测开发的延长时间表限制了传统诊断平台在低资源环境下的制造。为了解决这些挑战,我们描述了快速模块化纳米体检测(RAMONA),这是一种多功能抗原检测平台,利用纳米体卷曲的线圈融合蛋白与下游读出方法进行模块化集成。RAMONA将LFAs的可移植性与纳米体的优点(如更小的尺寸、更好的溶解度和与无细胞蛋白质合成系统的兼容性)结合在一起,实现了按需生物制造和对不同靶标的快速适应。我们通过检测三种不同的蛋白质靶点,在不同温度和孵育期间的稳健性,以及与唾液样品和无细胞合成的兼容性,证明了分析的普遍性。检测在30分钟内完成,结果与ELISA数据密切相关,所需资源最少。此外,RAMONA通过正交捕获探针同时支持三种抗原的多路检测。通过克服传统免疫测定法的一些局限性,RAMONA代表了快速、适应性强和可现场部署的抗原检测技术的重大进步。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A Rapid and Modular Nanobody Assay for Plug-and-Play Antigen Detection

A Rapid and Modular Nanobody Assay for Plug-and-Play Antigen Detection

Rapid and portable antigen detection is essential for managing infectious diseases and responding to toxic exposures, yet current methods face significant limitations. Highly sensitive platforms like the Enzyme-Linked Immunosorbent Assay (ELISA) are time- and cost-prohibitive for point-of-need detection, while portable options like lateral flow assays (LFAs) require systemic overhauls for new targets. Furthermore, the complex infrastructure, high production costs, and extended timelines for assay development constrain the manufacturing of traditional diagnostic platforms in low-resource settings. To address these challenges, we describe the Rapid and Modular Nanobody Assay (RAMONA), a versatile antigen detection platform that leverages nanobody-coiled coil fusion proteins for modular integration with downstream readout methods. RAMONA merges the portability of LFAs with the benefits of nanobodies such as their smaller size, improved solubility, and compatibility with cell-free protein synthesis systems, enabling on-demand biomanufacturing and rapid adaptation for diverse targets. We demonstrate assay generalizability through the detection of three distinct protein targets, robustness across various temperatures and incubation periods, and compatibility with saliva samples and cell-free synthesis. Detection occurs in under 30 minutes, with results strongly and positively correlating to ELISA data while requiring minimal resources. Moreover, RAMONA supports multiplexed detection of three antigens simultaneously by using orthogonal capture probes. By overcoming several limitations of traditional immunoassays, RAMONA represents a significant advancement in rapid, adaptable, and field-deployable antigen detection technologies.

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来源期刊
CiteScore
8.00
自引率
10.60%
发文量
380
审稿时长
6-12 weeks
期刊介绍: The journal is particularly interested in studies on the design and synthesis of new genetic circuits and gene products; computational methods in the design of systems; and integrative applied approaches to understanding disease and metabolism. Topics may include, but are not limited to: Design and optimization of genetic systems Genetic circuit design and their principles for their organization into programs Computational methods to aid the design of genetic systems Experimental methods to quantify genetic parts, circuits, and metabolic fluxes Genetic parts libraries: their creation, analysis, and ontological representation Protein engineering including computational design Metabolic engineering and cellular manufacturing, including biomass conversion Natural product access, engineering, and production Creative and innovative applications of cellular programming Medical applications, tissue engineering, and the programming of therapeutic cells Minimal cell design and construction Genomics and genome replacement strategies Viral engineering Automated and robotic assembly platforms for synthetic biology DNA synthesis methodologies Metagenomics and synthetic metagenomic analysis Bioinformatics applied to gene discovery, chemoinformatics, and pathway construction Gene optimization Methods for genome-scale measurements of transcription and metabolomics Systems biology and methods to integrate multiple data sources in vitro and cell-free synthetic biology and molecular programming Nucleic acid engineering.
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