基于非对称接触角复合界面的数字重组酶聚合酶扩增芯片

IF 5.7 2区 化学 Q1 CHEMISTRY, ANALYTICAL
Zhongping Zhang, Tianwei Li, Yao Tan, Luyao Liu, Hao Chen, Lulu Zhang, Michael G. Mauk, Xianbo Qiu
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引用次数: 0

摘要

背景数字重组酶聚合酶扩增(dRPA)是绝对量化核酸和检测罕见突变的有效工具。由于试剂的高粘度或其他物理特性,会影响检测结果的准确性和可重复性,从而限制了该技术的广泛采用和实际应用。在这项研究中,我们开发了非对称接触角数字等温检测(ACA-DID)芯片,并优化了ACA-DID芯片结构,以实现快速数字重组酶聚合酶扩增。在 PDMS 中添加表面活性剂可在流体通道的上下表面之间形成非对称接触角,从而改善试剂流动并促进试剂进入微孔。这种设计解决了高粘度试剂带来的挑战,高粘度试剂通常会使有效的数字离散化复杂化,并导致荧光信号聚集。通过稀释 RPA 试剂的特定成分,我们提高了扩增的均匀性,有效减少了信号聚集。结果疏水表面对核酸和蛋白质等生物大分子有很强的吸附性,会降低 dRPA 的扩增效率。为了实现试剂在微室中的高效扩增,这项工作采用了掺杂表面活性剂的 PDMS 表面修饰策略,从而消除了 PDMS 材料阻碍 dRPA 扩增效率的问题。这项创新有望克服当前数字 RPA 扩增平台的主要局限性,推动更广泛的采用和应用,尤其是在成本敏感或资源有限的环境中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Digital recombinase polymerase amplification chip based on asymmetric contact angle composite interface

Digital recombinase polymerase amplification chip based on asymmetric contact angle composite interface

Background

Digital recombinase polymerase amplification (dRPA) is an effective tool for the absolute quantification of nucleic acids and the detection of rare mutations. Due to the high viscosity or other physical properties of the reagent, this can compromise the accuracy and reproducibility of detection results, which limits the broader adoption and practical application of this technology. In this study, we developed an asymmetric contact angle digital isothermal detection (ACA-DID) chip and optimized the ACA-DID chip structure to achieve rapid digital recombinase polymerase amplification.

Result

We designed with a pressure-driven and highly asymmetric contact angle composite interface to enable robust digital RPA. The addition of surfactants to the PDMS creates an asymmetric contact angle between the upper and lower surfaces of the fluid channel, improving reagent flow and facilitating entry into microwells. This design addresses the challenges posed by high-viscosity reagents, which typically complicate effective digital discretization and lead to fluorescence signal aggregation. By diluting specific components of the RPA reagent, we improved the uniformity of amplification and effectively reduced signal aggregation. The hydrophobic surface of results strong adsorption to biological macromolecules, such as nucleic acids and proteins, which will decrease the efficiency of dRPA amplification. To achieve efficient amplification of reagents in the microchamber, this work uses a surface modification strategy of PDMS doped surfactant, which eliminates the issue of PDMS materials hindering dRPA amplification efficiency.

Significance and novelty

The ACA-DID chip demonstrated excellent analytical accuracy in the quantification of African swine fever DNA samples, highlighting its potential to enhance the accessibility and effectiveness of dRPA technology. This innovation promises to overcome key limitations in current digital RPA amplification platforms, driving broader adoption and application, especially in cost-sensitive or resource-limited settings.
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来源期刊
Analytica Chimica Acta
Analytica Chimica Acta 化学-分析化学
CiteScore
10.40
自引率
6.50%
发文量
1081
审稿时长
38 days
期刊介绍: Analytica Chimica Acta has an open access mirror journal Analytica Chimica Acta: X, sharing the same aims and scope, editorial team, submission system and rigorous peer review. Analytica Chimica Acta provides a forum for the rapid publication of original research, and critical, comprehensive reviews dealing with all aspects of fundamental and applied modern analytical chemistry. The journal welcomes the submission of research papers which report studies concerning the development of new and significant analytical methodologies. In determining the suitability of submitted articles for publication, particular scrutiny will be placed on the degree of novelty and impact of the research and the extent to which it adds to the existing body of knowledge in analytical chemistry.
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