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阐明研究不足的激酶:一种应用于蛋白激酶N的通用生物传感器开发方法。

Illuminating understudied kinases: a generalizable biosensor development method applied to protein kinase N.

作者信息

Bogomolovas Julius, Chen Ju

机构信息

Department of Medicine, UCSD, La Jolla, CA, USA.

出版信息

Commun Biol. 2025 Jan 22;8(1):109. doi: 10.1038/s42003-025-07510-4.

Abstract

Protein kinases play crucial roles in regulating cellular processes, making real-time visualization of their activity essential for understanding signaling dynamics. While genetically encoded fluorescent biosensors have emerged as powerful tools for studying kinase activity, their development for many kinases remains challenging due to the lack of suitable substrate peptides. Here, we present a novel approach for identifying peptide substrates and demonstrate its effectiveness by developing a biosensor for Protein Kinase N (PKN) activity. Our method identified a new PKN substrate peptide that we optimized for use in a fluorescent biosensor design. The resulting biosensor shows specificity for PKN family kinases and can detect both overexpressed and endogenous PKN activity in live cells. Importantly, our biosensor revealed sustained basal PKN2 activity at the plasma membrane, identifying it as a PKN2 activity hotspot. This work not only provides a valuable tool for studying PKN signaling but also demonstrates a promising strategy for developing biosensors for other understudied kinases, potentially expanding our ability to monitor kinase activity across the human kinome.

摘要

蛋白激酶在调节细胞过程中发挥着关键作用,因此对其活性进行实时可视化对于理解信号转导动力学至关重要。虽然基因编码的荧光生物传感器已成为研究激酶活性的强大工具,但由于缺乏合适的底物肽,针对许多激酶开发此类传感器仍具有挑战性。在此,我们提出了一种鉴定肽底物的新方法,并通过开发一种用于蛋白激酶N(PKN)活性的生物传感器来证明其有效性。我们的方法鉴定出一种新的PKN底物肽,并对其进行优化以用于荧光生物传感器设计。所得生物传感器对PKN家族激酶具有特异性,能够检测活细胞中过表达和内源性PKN的活性。重要的是,我们的生物传感器揭示了质膜上持续的基础PKN2活性,将其确定为PKN2活性热点。这项工作不仅为研究PKN信号传导提供了有价值的工具,还展示了一种为其他研究较少的激酶开发生物传感器的有前景的策略,有可能扩展我们监测人类激酶组中激酶活性的能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc17/11754634/6b1957bd08bc/42003_2025_7510_Fig1_HTML.jpg

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