通过佛斯特共振能量转移开发针对金属-β-内酰胺酶的灵敏传感器

Zeineb Ayed, Nathaniel Davis and Renee V Goreham
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引用次数: 0

摘要

细菌的抗生素耐药性问题日益严重,需要创新的检测方法来及时发现耐药性机制。在本研究中,我们提出了一种检测铜绿假单胞菌耐药性的新方法。铜绿假单胞菌是一种在抗生素耐药性发展过程中产生金属-β-内酰胺酶的细菌。我们利用两种不同的方法设计了一种采用佛斯特共振能量转移的适配传感器。起初,我们利用带有硫化锌外壳的磷化铟量子点和金纳米粒子作为佛斯特共振能量转移的供体-受体对。虽然该系统显示出响应,但效率很低。随后进行的优化包括将供体和受体靠近,并加入两个发射波长不同的量子点作为受体和供体。这一优化大大提高了福斯特共振效率,从而产生了一种检测金属-β-内酰胺酶的新方法。通过优化量子点-量子点对的距离和供体,福斯特共振能量传递效率从 31% 提高到 63%。我们的研究结果展示了一种廉价、快速、多用途的适配传感器,其潜在应用范围超出了抗生素耐药性的范畴,突出了它在不同应用场景下的适应性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development of an aptasensor to target metallo-β-lactamase through Förster resonance energy transfer
The escalating issue of antibiotic resistance in bacteria necessitates innovative detection methods to identify resistance mechanisms promptly. In this study, we present a novel approach for detecting resistance in Pseudomonas aeruginosa, a bacterium known for its metallo-β-lactamase production during the development of antibiotic resistance. We have designed an aptasensor employing Förster resonance energy transfer utilising two distinct methodologies. Initially, indium phosphide quantum dots with a zinc sulphide shell, and gold nanoparticles were utilised as the Förster resonance energy transfer donor-acceptor pair. Although this system demonstrated a response, the efficiency was low. Subsequently, optimisation involved relocating the donor and acceptor in close proximity and incorporating two quantum dots with varying emission wavelengths as the acceptor and donor. This optimisation significantly enhanced the Förster resonance efficiency, resulting in a novel method for detecting metallo-β-lactamase. Förster resonance energy transfer efficiency was increased from 31% to 63% by optimising the distance and donor using a quantum dot-quantum dot pair. Our findings showcase a cheap, rapid and versatile aptasensor with potential applications beyond antibiotic resistance, highlighting its adaptability for diverse scenarios.
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