Evidence map›Paper›PMID 30321182›Full record

ArticlePloS one2018

Calcium binding of the antifungal protein PAF: Structure, dynamics and function aspects by NMR and MD simulations.

Ádám Fizil, Christoph Sonderegger, András Czajlik, Attila Fekete, István Komáromi, Dorottya Hajdu, Florentine Marx, Gyula Batta

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.8field-weighted citation impact, top 30% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. TheJournal of fungi (Basel, Switzerland) · 2020
    Article
  5. Review
  6. Review
  7. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 2 countries.

Ádám FizilDepartment of Organic Chemistry, Faculty of Science and Technology, University of Debrecen, Debrecen, Hungary.
Christoph SondereggerDivision of Molecular Biology, Biocenter, Medical University of Innsbruck, Innsbruck, Austria.
András CzajlikDepartment of Organic Chemistry, Faculty of Science and Technology, University of Debrecen, Debrecen, Hungary.
Attila FeketeDepartment of Organic Chemistry, Faculty of Science and Technology, University of Debrecen, Debrecen, Hungary.
István KomáromiDivision of Clinical Laboratory Science, Department of Laboratory Medicine, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Dorottya HajduDepartment of Organic Chemistry, Faculty of Science and Technology, University of Debrecen, Debrecen, Hungary.
Florentine MarxDivision of Molecular Biology, Biocenter, Medical University of Innsbruck, Innsbruck, Austria.ORCID 0000-0002-8408-1842
Gyula BattaDepartment of Organic Chemistry, Faculty of Science and Technology, University of Debrecen, Debrecen, Hungary.ORCID 0000-0002-0442-1828
University of Debrecen · HUInnsbruck Medical University · AT

Funding

Austrian Science Fund FWF I 1644Austrian Science Fund FWF P 25894
6 · The paper itself

Abstract

Calcium ions (Ca2+) play an important role in the toxicity of the cysteine-rich and cationic antifungal protein PAF from Penicillium chrysogenum: high extracellular Ca2+ levels reduce the toxicity of PAF in the sensitive model fungus Neurospora crassa in a concentration dependent way. However, little is known about the mechanistic details of the Ca2+ ion impact and the Ca2+ binding capabilities of PAF outside the fungal cell, which might be the reason for the activity loss. Using nuclear magnetic resonance (NMR), isothermal titration calorimetry and molecular dynamics (MD) simulations we demonstrated that PAF weakly, but specifically binds Ca2+ ions. MD simulations of PAF predicted one major Ca2+ binding site at the C-terminus involving Asp53 and Asp55, while Asp19 was considered as putative Ca2+ binding site. The exchange of Asp19 to serine had little impact on the Ca2+ binding, however caused the loss of antifungal activity, as was shown in our recent study. Now we replaced the C-terminal aspartates and expressed the serine variant PAFD53S/D55S. The specific Ca2+ binding affinity of PAFD53S/D55S decreased significantly if compared to PAF, whereas the antifungal activity was retained. To understand more details of Ca2+ interactions, we investigated the NMR and MD structure/dynamics of the free and Ca2+-bound PAF and PAFD53S/D55S. Though we found some differences between these protein variants and the Ca2+ complexes, these effects cannot explain the observed Ca2+ influence. In conclusion, PAF binds Ca2+ ions selectively at the C-terminus; however, this Ca2+ binding does not seem to play a direct role in the previously documented modulation of the antifungal activity of PAF.

Indexed as

Binding SitesCalciumCalorimetryFungal ProteinsMagnetic Resonance SpectroscopyModels, MolecularMolecular Dynamics SimulationMutationNeurospora crassaPenicillium chrysogenumProtein BindingCalciumFungal ProteinsPAF protein, Penicillium chrysogenum

Identifiers

PMID30321182
PMCPMC6188699
OpenAlexW2896765558

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.