• Medientyp: E-Artikel
  • Titel: Total proteome turbidity assay for tracking global protein aggregation in the natural cellular environment
  • Beteiligte: Shmueli, Merav D.; Hizkiahou, Noa; Peled, Sivan; Gazit, Ehud; Segal, Daniel
  • Erschienen: Journal of Biological Methods, 2017
  • Erschienen in: Journal of Biological Methods, 4 (2017) 2, Seite e69
  • Sprache: Nicht zu entscheiden
  • DOI: 10.14440/jbm.2017.148
  • ISSN: 2326-9901
  • Entstehung:
  • Anmerkungen:
  • Beschreibung: Proteome homeostasis is crucial for optimal cellular function and survival in the face of various stressful impacts. This entails preservation of a balance between protein synthesis, folding, degradation, and trafficking collectively termed proteostasis. A hallmark of proteostasis failure, which underlies various diseases, is enhanced misfolding and aggregation of proteins. Here we adapted the measurement of protein turbidity, which is commonly used to evaluate aggregation of single purified proteins, for monitoring propensity for aggregation of the entire soluble cellular proteome incubated in vitro for several hours. We show that over-expression of an aggregation-prone protein or applying endoplasmic-reticulum (ER) stress to either cells in culture or to the intact organism, Drosophila, enhances the rise in turbidity of the global soluble proteome compared to untreated cells. Additionally, given that Alzheimer’s disease (AD) is known to involve ER stress and aggregation of proteins, we demonstrate that the soluble fraction of brain extracts from AD patients displays markedly higher rise of global proteome turbidity than in healthy counterparts. This assay could be valuable for various biological, medical and biotechnological applications.
  • Zugangsstatus: Freier Zugang