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用于活细胞中基于免洗单分子定位的超分辨率成像的自发眨眼探针

Spontaneously Blinkogenic Probe for Wash-Free Single-Molecule Localization-Based Super-Resolution Imaging in Living Cells.

作者信息

Qiao Qinglong, Song Aoxuan, An Kai, Xu Ning, Jia Wenhao, Ruan Yiyan, Bao Pengjun, Tao Yi, Zhang Yinchan, Wang Xiang, Xu Zhaochao

机构信息

Dalian Institute of Chemical Physics, Chinese Academy of Sciences, 457 Zhongshan Road, Dalian, 116023, China.

University of Chinese Academy of Sciences, Beijing, 100049, China.

出版信息

Angew Chem Int Ed Engl. 2025 Feb 3;64(6):e202417469. doi: 10.1002/anie.202417469. Epub 2024 Nov 21.

Abstract

Single-molecule localization super-resolution fluorescence imaging relies on the fluorescence ON/OFF switching of fluorescent probes to break the diffraction limit. However, the unreacted or nonspecifically bound probes cause non-targeted ON/OFF switching, resulting in substantial fluorescence background that significantly reduces localization precision and accuracy. Here, we report a blinkogenic probe HM-DS655-Halo that remains blinking OFF until it binds to HaloTag, thereby triggering its self-blinking activity and enabling its application in direct SMLM imaging in living cells without wash-out steps. We employed the ratio of the duty cycle before and after self-blinking activation, termed as the parameter "R" to characterize blinkogenicity. The covalent binding to HaloTag induces HM-DS655-Halo to transition from a fluorescent OFF state to a fluorescence blinking state. This transition also leads to a change in the R value, which is calculated to be 12, ensuring super blinkogenicity to effectively suppress background signals in living cells. HM-DS655-Halo was successfully applied in dynamic SMLM imaging of diverse intracellular sub-structures with minimal background noise, including mitochondrial fission and contact, cell migration, and pseudopod growth.

摘要

单分子定位超分辨率荧光成像依赖于荧光探针的荧光开/关切换来突破衍射极限。然而,未反应或非特异性结合的探针会导致非靶向的开/关切换,产生大量荧光背景,显著降低定位精度和准确性。在此,我们报道了一种可产生闪烁的探针HM-DS655-Halo,它在与HaloTag结合之前一直处于关闭闪烁状态,从而触发其自身的闪烁活性,并使其能够应用于活细胞的直接单分子定位超分辨率成像,无需洗脱步骤。我们采用自闪烁激活前后的占空比比值,即参数“R”来表征闪烁产生能力。与HaloTag的共价结合诱导HM-DS655-Halo从荧光关闭状态转变为荧光闪烁状态。这种转变也导致R值发生变化,经计算R值为12,确保了超强的闪烁产生能力,能有效抑制活细胞中的背景信号。HM-DS655-Halo已成功应用于多种细胞内亚结构的动态单分子定位超分辨率成像,背景噪声极小,包括线粒体分裂和接触、细胞迁移以及伪足生长。

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