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用于报告细胞相互作用的应激激活邻近标记

Stressor-Actuated Proximity Labeling for Reporting Cellular Interaction.

作者信息

Wang Guyu, Wang Yichun, Wang Lan, Wu Shijie, Cao Ao, Pu Wenyuan, Li Tielei, Xie Ran, Wang Hongwei, Ding Lin, Ju Huangxian

机构信息

State Key Laboratory of Analytical Chemistry for Life Science, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210023, China.

State Key Laboratory of Coordination Chemistry, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210023, China.

出版信息

Anal Chem. 2024 Dec 17;96(50):20065-20073. doi: 10.1021/acs.analchem.4c05008. Epub 2024 Dec 2.

Abstract

Cell-cell interactions determine the activation state and function of cells. When host cells are exposed to stressors such as microorganisms, immune defense machinery is activated to release HO, providing direct evidence of the relevant cellular physiological processes. Inspired by the fact that peroxidase can catalyze proximity labeling in the presence of exogenous HO, a stressor-actuated proximity labeling (SAPL) strategy is developed to report the process information on cell-cell interactions by recording stress levels. The stressors are covalently modified with horseradish peroxidase (HRP) and the HO released by the host cells in response to the stressors triggers HRP-based proximity labeling. Using a fungal mimic or live fungi as stressors, the stress levels of different host cells are compared by in situ imaging of the labeling signals. The ability to accumulate stress signals allows SAPL to more sensitively differentiate between interactions involving different macrophage phenotypes. SAPL is also a powerful tool for real-time, in situ monitoring of the effects of surface modifications on cellular interactions. Thus, the SAPL strategy represents a new perspective in the monitoring of cell-cell interactions using endogenous effector molecules.

摘要

细胞间相互作用决定细胞的激活状态和功能。当宿主细胞暴露于微生物等应激源时,免疫防御机制被激活以释放HO,这为相关细胞生理过程提供了直接证据。受过氧化物酶在外源HO存在下可催化邻近标记这一事实的启发,开发了一种应激源驱动的邻近标记(SAPL)策略,通过记录应激水平来报告细胞间相互作用的过程信息。应激源用辣根过氧化物酶(HRP)进行共价修饰,宿主细胞响应应激源释放的HO触发基于HRP的邻近标记。使用真菌模拟物或活真菌作为应激源,通过标记信号的原位成像比较不同宿主细胞的应激水平。积累应激信号的能力使SAPL能够更灵敏地区分涉及不同巨噬细胞表型的相互作用。SAPL也是实时原位监测表面修饰对细胞相互作用影响的有力工具。因此,SAPL策略代表了利用内源性效应分子监测细胞间相互作用的新视角。

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