Xu Xiao, Xiao Lu, Gu Chunmei, Shang Jiachen, Xiang Yu
Department of Chemistry, Beijing Key Laboratory for Microanalytical Methods and Instrumentation, Key Laboratory of Bioorganic Phosphorus Chemistry and Chemical Biology (Ministry of Education), Tsinghua University, Beijing 100084, China.
ACS Omega. 2021 May 12;6(20):13153-13160. doi: 10.1021/acsomega.1c00976. eCollection 2021 May 25.
RNA-cleaving DNAzymes are widely applied as sensors for detecting metal ions in environmental samples owing to their high sensitivity and selectivity, but their use for sensing biological metal ions in live cells is challenging because constitutive sensors fail to report the spatiotemporal heterogeneity of biological processes. Photocaged DNAzymes can be activated by light for sensing purposes that need spatial and temporal resolution. Studying complex biological processes requires logic photocontrol, but unfortunately all the literature-reported photocaged DNAzymes working in live cells cannot be selectively controlled by light irradiation at different wavelengths. In this work, we developed photocaged DNAzymes responsive to UV and visible light using a general synthetic method based on phosphorothioate chemistry. Taking the Zn-dependent DNAzyme sensor as a model, we achieved wavelength-selective activation of photocaged DNAzymes in live human cells by UV and visible light, laying the groundwork for the logic activation of DNAzyme-based sensors in biological systems.
RNA切割型脱氧核酶因其高灵敏度和选择性而被广泛用作检测环境样品中金属离子的传感器,但将其用于检测活细胞中的生物金属离子具有挑战性,因为组成型传感器无法报告生物过程的时空异质性。光笼式脱氧核酶可通过光激活,用于需要空间和时间分辨率的传感目的。研究复杂的生物过程需要逻辑光控,但不幸的是,所有文献报道的在活细胞中起作用的光笼式脱氧核酶都不能通过不同波长的光照射进行选择性控制。在这项工作中,我们基于硫代磷酸酯化学,采用通用合成方法开发了对紫外光和可见光有响应的光笼式脱氧核酶。以锌依赖性脱氧核酶传感器为模型,我们通过紫外光和可见光在活的人类细胞中实现了光笼式脱氧核酶的波长选择性激活,为生物系统中基于脱氧核酶的传感器的逻辑激活奠定了基础。