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@ARTICLE{Hoenigsperger:285359,
author = {Hoenigsperger, Helene and Klute, Susanne and Engels, Zoe
and Volcic, Meta and Sparrer, Konstantin Maria Johannes},
title = {{P}rotocol to differentially quantify spatially resolved
viral protein-cellular protein interactions via proximity
ligation assays.},
journal = {STAR Protocols},
volume = {7},
number = {1},
issn = {2666-1667},
address = {Cambridge, MA},
publisher = {Cell Press},
reportid = {DZNE-2026-00224},
pages = {104361},
year = {2026},
abstract = {The spatial organization of viral and cellular proteins
shapes signal transduction. Here, we present a protocol to
quantify differential protein-protein interactions by
measuring their spatial association using proximity ligation
assays (PLAs). We describe steps for seeding, transfection,
proximity labeling, and confocal microscopy imaging and
provide procedures for quantitative analysis. Our approach
complements co-immunoprecipitation-based interactome data by
enabling in situ quantification of differential binding
between cellular and viral interaction partners. For
complete details on the use and execution of this protocol,
please refer to Klute et al.1.},
keywords = {Antibody (Other) / Immunology (Other) / In Situ
Hybridization (Other) / Microbiology (Other) /
Molecular/Chemical Probes (Other)},
cin = {AG Sparrer},
ddc = {600},
cid = {I:(DE-2719)1910003},
pnm = {351 - Brain Function (POF4-351)},
pid = {G:(DE-HGF)POF4-351},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:41686640},
pmc = {pmc:PMC12915154},
doi = {10.1016/j.xpro.2026.104361},
url = {https://pub.dzne.de/record/285359},
}