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用于突显活细胞中激酶活性的光控积分器。

Light-gated Integrator for Highlighting Kinase Activity in Living Cells.

作者信息

Lin Wei, Phatarphekar Abhishek, Zhong Yanghao, Liu Longwei, Kwon Hyung-Bae, Gerwick William H, Wang Yingxiao, Mehta Sohum, Zhang Jin

机构信息

Department of Pharmacology, University of California San Diego, La Jolla, CA, USA.

Alfred E. Mann Department of Biomedical Engineering, University of Southern California, Los Angeles, CA, USA.

出版信息

bioRxiv. 2024 Mar 20:2024.03.18.585554. doi: 10.1101/2024.03.18.585554.

Abstract

Protein kinases are key signaling nodes that regulate fundamental biological and disease processes. Illuminating kinase signaling from multiple angles can provide deeper insights into disease mechanisms and improve therapeutic targeting. While fluorescent biosensors are powerful tools for visualizing live-cell kinase activity dynamics in real time, new molecular tools are needed that enable recording of transient signaling activities for post hoc analysis and targeted manipulation. Here, we develop a light-gated kinase activity coupled transcriptional integrator (KINACT) that converts dynamic kinase signals into "permanent" fluorescent marks. KINACT enables robust monitoring of kinase activity across scales, accurately recording subcellular PKA activity, highlighting PKA signaling heterogeneity in 3D cultures, and identifying PKA activators and inhibitors in high-throughput screens. We further leverage the ability of KINACT to drive signaling effector expression to allow feedback manipulation of the balance of Gα-induced PKA and ERK activation and dissect the mechanisms of oncogenic G protein signaling.

摘要

蛋白激酶是调节基本生物学和疾病过程的关键信号节点。从多个角度阐明激酶信号传导可以更深入地了解疾病机制,并改善治疗靶点。虽然荧光生物传感器是实时可视化活细胞激酶活性动态的强大工具,但仍需要新的分子工具来记录瞬时信号活动,以便进行事后分析和靶向操作。在这里,我们开发了一种光门控激酶活性偶联转录整合器(KINACT),它将动态激酶信号转化为“永久性”荧光标记。KINACT能够在多个尺度上对激酶活性进行稳健监测,准确记录亚细胞PKA活性,突出3D培养物中PKA信号的异质性,并在高通量筛选中鉴定PKA激活剂和抑制剂。我们进一步利用KINACT驱动信号效应器表达的能力,对Gα诱导的PKA和ERK激活的平衡进行反馈操作,并剖析致癌G蛋白信号传导的机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25f0/10983958/399f2964dcd4/nihpp-2024.03.18.585554v1-f0001.jpg

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