用化学标记对细胞蛋白激酶活性进行分子记录

De-en Sun, Siu Wang Ng, Yu Zheng, Shu Xie, Niklas Schwan, Paula Breuer, Dirk C. Hoffmann, Julius Michel, Daniel D. Azorin, Kim E. Boonekamp, Frank Winkler, Wolfgang Wick, Michael Boutros, Yulong Li, Kai Johnsson
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引用次数: 0

摘要

蛋白激酶控制着大多数细胞过程,激酶活性异常与许多疾病有关。为了研究异质细胞群和体内特定激酶活性与细胞表型之间的联系,我们引入了激酶活性分子记录器,以便日后进行分析。我们的记录器基于分离式 HaloTag 和磷酸化依赖性分子开关,在存在特定激酶活性和荧光 HaloTag 底物的情况下会迅速被标记。特定细胞中的激酶活性控制着荧光标记的程度,而记录窗口则由荧光底物的存在来设定。我们将蛋白激酶 A 记录器应用于异质细胞群的分选和随后的转录组分析,在全基因组 CRISPR 筛选中发现 PKA 活性的调节因子,并跟踪自由移动小鼠的神经调制。
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Molecular recording of cellular protein kinase activity with chemical labeling
Protein kinases control most cellular processes and aberrant kinase activity is involved in numerous diseases. To investigate the link between specific kinase activities and cellular phenotypes in heterogeneous cell populations and in vivo, we introduce molecular recorders of kinase activities for later analysis. Based on split-HaloTag and a phosphorylation-dependent molecular switch, our recorders become rapidly labeled in the presence of a specific kinase activity and a fluorescent HaloTag substrate. The kinase activity in a given cell controls the degree of fluorescent labeling whereas the recording window is set by the presence of the fluorescent substrate. We have designed specific recorders for four protein kinases, including protein kinase A. We apply our protein kinase A recorder for the sorting of heterogeneous cell populations and subsequent transcriptome analysis, in genome-wide CRISPR screens to discover regulators of PKA activity and for the tracking of neuromodulation in freely moving mice.
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