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@ARTICLE{Sun:302830,
author = {D.-E. Sun and S. W. Ng$^*$ and Y. Zheng and S. Xie and N.
Schwan and P. Breuer and D. C. F. Hoffmann$^*$ and J. J.
Michel$^*$ and D. D. Azorin$^*$ and K. E. Boonekamp$^*$ and
F. Winkler$^*$ and W. Wick$^*$ and M. Boutros$^*$ and Y. Li
and K. Johnsson},
title = {{M}olecular recording of cellular protein kinase activity
with chemical labeling.},
journal = {Nature chemical biology},
volume = {nn},
issn = {1552-4450},
address = {Basingstoke},
publisher = {Nature Publishing Group},
reportid = {DKFZ-2025-01370},
pages = {nn},
year = {2025},
note = {epub},
abstract = {Protein kinases control most cellular processes and
aberrant kinase activity is involved in numerous diseases.
Here we introduce molecular recorders of kinase activities
for later analysis to investigate the link between specific
kinase activities and cellular phenotypes in heterogeneous
cell populations and in vivo. 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 designed specific
recorders for four protein kinases, including protein kinase
A. We apply our protein kinase A recorder to sort
heterogeneous cell populations for subsequent transcriptome
analysis, in genome-wide CRISPR screens to discover
regulators of PKA activity and to track neuromodulation in
freely moving mice.},
cin = {B110 / B320 / HD01},
ddc = {570},
cid = {I:(DE-He78)B110-20160331 / I:(DE-He78)B320-20160331 /
I:(DE-He78)HD01-20160331},
pnm = {312 - Funktionelle und strukturelle Genomforschung
(POF4-312)},
pid = {G:(DE-HGF)POF4-312},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:40640555},
doi = {10.1038/s41589-025-01949-6},
url = {https://inrepo02.dkfz.de/record/302830},
}