Department of Nanoengineering, University of California, La Jolla, San Diego, California 92093, United States.
Materials Science and Engineering Program, University of California, La Jolla, San Diego, California 92093, United States.
ACS Appl Mater Interfaces. 2021 Sep 29;13(38):45236-45243. doi: 10.1021/acsami.1c11620. Epub 2021 Sep 14.
Gold nanorods possess optical properties that are tunable and highly sensitive to variations in their aspect ratio (length/width). Therefore, the development of a sensing platform where the gold nanorod morphology (i.e., aspect ratio) is modulated in response to an analyte holds promise in achieving ultralow detection limits. Here, we use a dithiol peptide as an enzyme substrate during nanorod growth. The sensing mechanism is enabled by the substrate design, where the dithiol peptide contains an enzyme cleavage site in-between cysteine amino acids. When cleaved, the peptide dramatically impacts gold nanorod growth and the resulting optical properties. We demonstrate that the optical response can be correlated with enzyme concentration and achieve a 45 pM limit of detection. Furthermore, we extend this sensing platform to colorimetrically detect tumor-associated inhibitors in a biologically relevant medium. Overall, these results present a subnanomolar method to detect proteases that are critical biomarkers found in cancers, infectious diseases, and inflammatory disorders.
金纳米棒具有可调谐的光学特性,对其纵横比(长度/宽度)的变化非常敏感。因此,开发一种能够根据分析物调节金纳米棒形态(即纵横比)的传感平台,有望实现超低的检测限。在这里,我们在纳米棒生长过程中使用二硫肽作为酶的底物。该传感机制得益于底物的设计,其中二硫肽在半胱氨酸氨基酸之间包含一个酶切割位点。被切割后,该肽会显著影响金纳米棒的生长和由此产生的光学特性。我们证明,光学响应可以与酶浓度相关联,并实现 45 pM 的检测限。此外,我们将这个传感平台扩展到在生物相关介质中比色检测肿瘤相关抑制剂。总的来说,这些结果提出了一种亚纳摩尔的方法来检测蛋白酶,这些蛋白酶是癌症、传染病和炎症性疾病中关键的生物标志物。