Publications by authors named "D Maltseva"

Article Synopsis
  • * Researchers have created model peptides resembling CAHS proteins and tested them to understand their structural changes when exposed to desiccation-like conditions.
  • * Findings indicate that these peptides, which are mainly disordered, form more structured, helical shapes under desiccation, suggesting they could help develop new synthetic materials for protection against drying.
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Article Synopsis
  • A study highlights that using shRNA-based methods for miRNA overexpression, especially for certain miRNAs from polycistronic clusters, can lead to unintentional creation of 5' end isoforms (5'-isomiRs) that differ from the intended miRNA, affecting research accuracy.
  • The transcription process of shRNAs via RNA Polymerase III can add extra nucleotides, altering the cleavage site and resulting in 5'-isomiRs with changed seed regions, which impacts their function.
  • Standard qPCR methods fail to detect these alterations, highlighting the need for miRNA-Seq analysis to accurately assess miRNA expression and their regulation of mRNA targets, emphasizing careful design for shRNA constructs.
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The organic nucleation of the pharmaceutical ibuprofen is investigated, as triggered by the protonation of ibuprofen sodium salt at elevated pH. The growth and aggregation of nanoscale solution species by Analytical Ultracentrifugation and Molecular Dynamics (MD) simulations is tracked. Both approaches reveal solvated molecules, oligomers, and prenucleation clusters, their size as well as their hydration at different reaction stages.

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Since its original discovery over a decade ago, extracellular RNA (exRNA) has been found in all biological fluids. Furthermore, extracellular microRNA has been shown to be involved in communication between various cell types. Importantly, the exRNA is protected from RNases degradation by certain carriers including membrane vesicles and non-vesicular protein nanoparticles.

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Alternative splicing is often deregulated in cancer, and cancer-specific isoform switches are part of the oncogenic transformation of cells. Accumulating evidence indicates that isoforms of the multifunctional cell-surface glycoprotein CD44 play different roles in cancer cells as compared to normal cells. In particular, the shift of CD44 isoforms is required for epithelial to mesenchymal transition (EMT) and is crucial for the maintenance of pluripotency in normal human cells and the acquisition of cancer stem cells phenotype for malignant cells.

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