| Article ID | Journal | Published Year | Pages | File Type | 
|---|---|---|---|---|
| 10870315 | FEBS Letters | 2015 | 6 Pages | 
Abstract
												The Penicillium chrysogenum antifungal protein PAF is toxic against potentially pathogenic Ascomycetes. We used the highly sensitive aequorin-expressing model Aspergillus niger to identify a defined change in cytoplasmic free Ca2+ dynamics in response to PAF. This Ca2+ signature depended on an intact positively charged lysine-rich PAF motif. By combining Ca2+ measurements in A. niger mutants with deregulated cAMP/protein kinase A (PKA) signaling, we proved the interconnection of Ca2+ perturbation and cAMP/PKA signaling in the mechanistic function of PAF. A deep understanding of the mode of action of PAF is an invaluable prerequisite for its future application as new antifungal drug.
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											Authors
												Ulrike Binder, Mojca BenÄina, Ádám Fizil, Gyula Batta, Anil K. Chhillar, Florentine Marx, 
											