Sescil Jennifer, Fiel Hailey, Havens Steven M, Fu Emma, Li Xingyu, Kroning Kayla E, Solowiej Isabel, Li Peng, Wang Wenjing
Department of Chemistry, University of Michigan Ann Arbor MI 48109 USA
Life Sciences Institute, University of Michigan Ann Arbor MI 48109 USA.
RSC Chem Biol. 2025 Feb 18;6(4):555-562. doi: 10.1039/d4cb00276h. eCollection 2025 Apr 2.
Genetically encoded fluorescent sensors have been widely applied to detect cell signaling molecules and events. We previously designed a fluorescent sensor motif suitable for detecting protease activity and opioids. In this manuscript, we demonstrated the motif's first use for reporting on protease activity in animal models, demonstrating a high signal-to-background ratio of 29. We further functionalized this sensor motif to detect the activity of the coronavirus main protease, Mpro, and demonstrated its utility in characterizing an Mpro inhibitor. The Mpro sensor will facilitate the study of coronaviral activity in cell cultures and potentially in animal models. Additionally, we developed an innovative method for engineering a protease-based time-gating mechanism using this versatile sensor motif, allowing the temporally controlled detection of opioids. This time-gating strategy for detecting opioids can be generalized to other similar sensors, enabling detection of G protein-coupled receptor ligands with improved temporal resolution.
基因编码荧光传感器已被广泛应用于检测细胞信号分子和事件。我们之前设计了一种适用于检测蛋白酶活性和阿片类药物的荧光传感器基序。在本手稿中,我们展示了该基序首次用于在动物模型中报告蛋白酶活性,显示出高达29的高信号背景比。我们进一步对该传感器基序进行功能化,以检测冠状病毒主要蛋白酶Mpro的活性,并证明了其在表征Mpro抑制剂方面的效用。Mpro传感器将有助于研究细胞培养物中以及潜在地在动物模型中的冠状病毒活性。此外,我们开发了一种创新方法,利用这种通用的传感器基序构建基于蛋白酶的时间门控机制,从而实现对阿片类药物的时间控制检测。这种检测阿片类药物的时间门控策略可以推广到其他类似传感器,从而能够以更高的时间分辨率检测G蛋白偶联受体配体。