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酵母双亲和生物砖:迈向可再生全细胞生物传感器的进展。

Yeast dual-affinity biobricks: Progress towards renewable whole-cell biosensors.

机构信息

Department of Electrical and Computer Engineering, University of California, San Diego, La Jolla, CA 92093, USA.

School of Medicine, University of California, San Diego, La Jolla, CA 92093, USA.

出版信息

Biosens Bioelectron. 2015 Aug 15;70:462-8. doi: 10.1016/j.bios.2015.03.044. Epub 2015 Mar 21.

Abstract

Point-of-care (POC) diagnostic biosensors offer a promising solution to improve healthcare, not only in developed parts of the world, but also in resource limited areas that lack adequate medical infrastructure and trained technicians. However, in remote and resource limited settings, cost and storage of traditional POC immunoassays often limit actual deployment. Synthetically engineered biological components ("BioBricks") provide an avenue to reduce costs and simplify assay procedures. In this article, the design and development of an ultra-low cost, whole-cell "renewable" capture reagent for use in POC diagnostic applications is described. Yeast cells were genetically modified to display both single chain variable fragment (scFv) antibodies and gold-binding peptide (GBP) on their surfaces for simple one step enrichment and surface functionalization. Electrochemical impedance spectroscopy (EIS) and fluorescent imaging were used to verify and characterize the binding of cells to gold electrodes. A complete electrochemical detection assay was then performed on screen-printed electrodes fixed with yeast displaying scFv directed to Salmonella outer membrane protein D (OmpD). Electrochemical assays were optimized and cross-validated with established fluorescence techniques. Nanomolar detection limits were observed for both formats.

摘要

即时检测 (POC) 诊断生物传感器为改善医疗保健提供了一个很有前景的解决方案,不仅在世界发达地区如此,在缺乏足够医疗基础设施和训练有素的技术人员的资源有限地区也是如此。然而,在偏远和资源有限的环境中,传统 POC 免疫分析的成本和储存往往限制了实际应用。合成工程生物组件 ("BioBricks") 为降低成本和简化分析程序提供了一种途径。在本文中,描述了一种超低成本的全细胞 "可再生" 捕获试剂的设计和开发,用于 POC 诊断应用。通过基因修饰酵母细胞,使其表面同时表达单链可变片段 (scFv) 抗体和金结合肽 (GBP),用于简单的一步富集和表面功能化。电化学阻抗谱 (EIS) 和荧光成像用于验证和表征细胞与金电极的结合。然后在固定有 scFv 的酵母上进行了全电化学检测分析,该 scFv 针对沙门氏菌外膜蛋白 D (OmpD)。对电化学检测进行了优化,并与已建立的荧光技术进行了交叉验证。两种方法都观察到纳摩尔级的检测限。

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