Publications by authors named "Joanna Toporowska"

Article Synopsis
  • The study focuses on selecting reliable reference genes (RGs) for reverse transcription quantitative PCR (RT-qPCR) in Avena sativa (oats) infected by Blumeria graminis, a major fungal pathogen causing powdery mildew.
  • Nine candidate RGs were tested across different oat lines and time points to determine their expression stability using four different algorithms.
  • The best RG combination identified was HNR (heterogeneous nuclear ribonucleoprotein 27 C) and EIF4A (eukaryotic initiation factor 4 A‑3), while TUA (α-tubulin) was found to be the least stable option for normalizing gene expression data.
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G Protein Coupled Receptors (GPCRs) constitute the largest family of signalling proteins responsible for translating extracellular stimuli into intracellular functions. They play crucial roles in numerous physiological processes and are major targets for drug discovery. Dysregulation of GPCRs is implicated in various diseases, making understanding their structural dynamics critical for therapeutic development.

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SARS-CoV-2 spike glycoprotein mediates receptor binding and subsequent membrane fusion. It exists in a range of conformations, including a closed state unable to bind the ACE2 receptor, and an open state that does so but displays more exposed antigenic surface. Spikes of variants of concern (VOCs) acquired amino acid changes linked to increased virulence and immune evasion.

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G-protein-coupled receptors signal through cognate G proteins. Despite the widespread importance of these receptors, their regulatory mechanisms for G-protein selectivity are not fully understood. Here we present a native mass spectrometry-based approach to interrogate both biased signalling and allosteric modulation of the β-adrenergic receptor in response to various ligands.

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A reliable qPCR experiment requires the selection of reference genes with a stable level of expression in a given experimental system. This study attempts to determine the reference genes (RGs) for the A. sativa-P.

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In this study we evaluated eleven candidate reference genes in Avena sativa during compatible and incompatible interactions with two different pathotypes of Puccinia coronata f. sp. avenae in six time points post-inoculation.

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