Wang Lele, Guo Ruiyan, Li Lanying, Tao Qing, Xu Qin, Yang Xue, Liu Xue, Li Jiang, Wang Lihua, Chang Jinxue, Cao Chengming, Wen Yanli, Song Shiping, Liu Gang
Key Laboratory of Bioanalysis and Metrology for state market regulation, Shanghai Institute of Measurement and Testing Technology, Shanghai 201203, China.
Institute of Materiobiology, Department of Chemistry, College of Science, Shanghai University, Shanghai 200444, China.
JACS Au. 2023 Dec 19;4(1):228-236. doi: 10.1021/jacsau.3c00673. eCollection 2024 Jan 22.
Intracellular enzyme cascades are essential for various biological processes, and mimicking their functions in artificial systems has attracted significant research attention. However, achieving convenient and efficient spatial organization of enzymes on interfaces remains a critical challenge. In this work, we designed a simple single-DNA scaffold using triblock polyA single-stranded DNA for the arrangement of coupled enzymes. The scaffold was assembled onto a gold electrode through the affinity of polyA-Au, and two enzymes (glucose oxidase and horseradish peroxidase) were captured through hybridization. The molecular distance between the enzymes was regulated by changing the length of the polyA fragment. As a proof of concept, a glucose biosensor was constructed based on the enzyme cascade amplification. The biosensor exhibited excellent detection capability for glucose in human serum samples with a limit of detection of 1.6 μM. Additionally, a trienzyme cascade reaction was successfully activated, demonstrating the potential scalability of our approach for multienzyme reactions. This study provides a promising platform for the development of easy-to-operate, highly efficient, and versatile enzyme cascade systems using DNA scaffolds.
细胞内酶级联反应对于各种生物过程至关重要,在人工系统中模拟其功能已引起了大量研究关注。然而,在界面上实现酶的便捷高效空间组织仍然是一项关键挑战。在这项工作中,我们设计了一种使用三嵌段聚腺苷单链DNA的简单单DNA支架来排列偶联酶。该支架通过聚腺苷与金的亲和力组装到金电极上,并通过杂交捕获两种酶(葡萄糖氧化酶和辣根过氧化物酶)。通过改变聚腺苷片段的长度来调节酶之间的分子距离。作为概念验证,基于酶级联放大构建了一种葡萄糖生物传感器。该生物传感器对人血清样本中的葡萄糖具有出色的检测能力,检测限为1.6 μM。此外,成功激活了三酶级联反应,证明了我们的方法在多酶反应方面具有潜在的可扩展性。这项研究为使用DNA支架开发易于操作、高效且通用的酶级联系统提供了一个有前景的平台。