All Stories

  1. The limits of prediction: Why intrinsically disordered regions challenge our understanding of antimicrobial peptides
  2. The N-terminal helix of MarA as a key element in the mechanism of DNA binding
  3. Structural assembly of the bacterial essential interactome
  4. The C-Terminus of Panusin, a Lobster β-Defensin, Is Crucial for Optimal Antimicrobial Activity and Serum Stability
  5. The PRALINE database: protein and Rna humAn singLe nucleotIde variaNts in condEnsates
  6. Antimicrobial Peptides Can Generate Tolerance by Lag and Interfere with Antimicrobial Therapy
  7. Analysis of Host–Bacteria Protein Interactions Reveals Conserved Domains and Motifs That Mediate Fundamental Infection Pathways
  8. A high‐throughput approach to predict A‐to‐I effects on RNA structure indicates a change of double‐stranded content in noncoding RNAs
  9. Examining Topoisomers of a Snake-Venom-Derived Peptide for Improved Antimicrobial and Antitumoral Properties
  10. Essential Role of Enzymatic Activity in the Leishmanicidal Mechanism of the Eosinophil Cationic Protein (RNase 3)
  11. In Vivo Evaluation of ECP Peptide Analogues for the Treatment of Acinetobacter baumannii Infection
  12. HPIPred: Host–pathogen interactome prediction with phenotypic scoring
  13. Rationally Modified Antimicrobial Peptides from the N-Terminal Domain of Human RNase 3 Show Exceptional Serum Stability
  14. The Interplay Between Disordered Regions in RNAs and Proteins Modulates Interactions Within Stress Granules and Processing Bodies
  15. Time-Resolved Transcriptional Profiling of Epithelial Cells Infected by Intracellular Acinetobacter baumannii
  16. Bacteria use structural imperfect mimicry to hijack the host interactome
  17. Human RNase3 immune modulation by catalytic-dependent and independent modes in a macrophage-cell line infection model
  18. DualSeqDB: the host–pathogen dual RNA sequencing database for infection processes
  19. RNA-binding and prion domains: the Yin and Yang of phase separation
  20. BacFITBase: a database to assess the relevance of bacterial genes during host infection
  21. Insight into the Antifungal Mechanism of Action of Human RNase N-terminus Derived Peptides
  22. A Coordinated Response at The Transcriptome and Interactome Level is Required to Ensure Uropathogenic Escherichia coli Survival during Bacteremia
  23. The fitness cost and benefit of phase‐separated protein deposits
  24. Cells alter their tRNA abundance to selectively regulate protein synthesis during stress conditions
  25. Positional scanning library applied to the human eosinophil cationic protein/RNase3 N-terminus reveals novel and potent anti-biofilm peptides
  26. Structural similarities in the CPC clip motif explain peptide-binding promiscuity between glycosaminoglycans and lipopolysaccharides
  27. Centrality in the host–pathogen interactome is associated with pathogen fitness during infection
  28. Structural basis for endotoxin neutralization by the eosinophil cationic protein
  29. Biofilm erradication by eosinophil cationic protein
  30. Insights into the Antimicrobial Mechanism of Action of Human RNase6: Structural Determinants for Bacterial Cell Agglutination and Membrane Permeation
  31. Is membrane homeostasis the missing link between inflammation and neurodegenerative diseases?
  32. Prediction of Bioactive Peptides Using Artificial Neural Networks
  33. Ribonucleases as a host-defence family: evidence of evolutionarily conserved antimicrobial activity at the N-terminus
  34. Towards the rational design of antimicrobial proteins
  35. Two Human Host Defense Ribonucleases against Mycobacteria, the Eosinophil Cationic Protein (RNase 3) and RNase 7
  36. Exploring New Biological Functions of Amyloids: Bacteria Cell Agglutination Mediated by Host Protein Aggregation
  37. Evolutionary selection for protein aggregation
  38. The “CPC Clip Motif”: A Conserved Structural Signature for Heparin-Binding Proteins
  39. Discovering New In Silico Tools for Antimicrobial Peptide Prediction
  40. Antimicrobial Peptide Action on Parasites
  41. Antimicrobial Action and Cell Agglutination by the Eosinophil Cationic Protein Are Modulated by the Cell Wall Lipopolysaccharide Structure
  42. Structural determinants of the eosinophil cationic protein antimicrobial activity
  43. Lipopolysaccharide Neutralization by Antimicrobial Peptides: A Gambit in the Innate Host Defense Strategy
  44. AMPA: an automated web server for prediction of protein antimicrobial regions
  45. The Generation of Antimicrobial Peptide Activity: A Trade-off between Charge and Aggregation?
  46. The Generation of Antimicrobial Peptide Activity: A Trade-off between Charge and Aggregation?
  47. Refining the Eosinophil Cationic Protein Antibacterial Pharmacophore by Rational Structure Minimization
  48. The role of Gram-negative envelope LPS on the bactericidal properties of proteins and peptides: the case of eosinophil cationic protein
  49. Towards the rational design of antimicrobial peptides: Recent developments in computational tools
  50. Connecting Peptide Physicochemical and Antimicrobial Properties by a Rational Prediction Model
  51. Mapping the eosinophil cationic protein antimicrobial activity by chemical and enzymatic cleavage
  52. Eosinophil Cationic Protein Aggregation: Identification of an N-Terminus Amyloid Prone Region
  53. Eosinophil cationic protein (ECP) can bind heparin and other glycosaminoglycans through its RNase active site
  54. Comparison of human RNase 3 and RNase 7 bactericidal action at the Gram-negative and Gram-positive bacterial cell wall
  55. Bactericidal and membrane disruption activities of the eosinophil cationic protein are largely retained in an N-terminal fragment
  56. Comparison of the membrane interaction mechanism of two antimicrobial RNases: RNase 3/ECP and RNase 7
  57. A theoretical approach to spot active regions in antimicrobial proteins
  58. The Antipathogen Activities of Eosinophil Cationic Protein
  59. Eosinophil Cationic Protein High-Affinity Binding to Bacteria-Wall Lipopolysaccharides and Peptidoglycans†
  60. Topography Studies on the Membrane Interaction Mechanism of the Eosinophil Cationic Protein †