Leslie Dan Faculty of Pharmacy, University of Toronto, Toronto, Ontario M5S 3M2, Canada.
ACS Nano. 2022 Jan 25;16(1):29-37. doi: 10.1021/acsnano.1c05766. Epub 2021 Dec 6.
Nonspecific binding is a significant challenge associated with biosensors in complex food textures. To overcome this, we have developed LISzymes, which are DNAzymes incorporated in lubricant-infused surfaces (LISs). Using milk as a complex background matrix, we show that LISzyme biosensors are significantly more effective in preventing nonspecific binding compared to other commonly used "blocking" methods. The use of lubricant infusion to treat sensing surfaces results in a 4-fold increase in the signal-to-noise ratio obtained with the DNAzyme with respect to untreated surfaces, when detecting the presence of specific bacteria in milk. This is a striking improvement upon previous DNAzyme sensors. We also show that the use of LISs does not affect the DNAzyme's ability to effectively and specifically detect its target─a protein specifically produced by (), in a complex sample matrix such as milk. LISzymes drastically improve DNAzyme performance, resulting in target detection associated with at concentrations as low as 250 CFU/mL in milk in less than an hour, which is currently not possible using other optical platforms. LISzymes are promising tools for the real-time monitoring of food contamination and may prove valuable within many other biosensing applications.
非特异性结合是与复杂食品质地中的生物传感器相关的重大挑战。为了克服这一问题,我们开发了 LISzymes,它是整合在润滑剂注入表面(LIS)中的 DNAzyme。我们使用牛奶作为复杂的背景基质,表明与其他常用的“阻断”方法相比,LISzyme 生物传感器在防止非特异性结合方面更有效。使用润滑剂注入来处理传感表面,与未处理表面相比,在检测牛奶中特定细菌的存在时,获得的 DNAzyme 的信噪比提高了 4 倍。这是对以前的 DNAzyme 传感器的显著改进。我们还表明,LIS 的使用不会影响 DNAzyme 有效且特异性地检测其靶标的能力——在牛奶等复杂样本基质中,专门由 () 产生的一种蛋白质。LISzymes 极大地改善了 DNAzyme 的性能,导致在牛奶中浓度低至 250 CFU/mL 的目标检测在不到一个小时内即可完成,这目前使用其他光学平台是不可能的。LISzymes 是实时监测食品污染的有前途的工具,并且可能在许多其他生物传感应用中证明是有价值的。