Methods for measuring misfolded protein clearance in the budding yeast Saccharomyces cerevisiae

Methods Enzymol. 2019:619:27-45. doi: 10.1016/bs.mie.2018.12.039. Epub 2019 Feb 8.

Abstract

Protein misfolding in the cell is linked to an array of diseases, including cancers, cardiovascular disease, type II diabetes, and numerous neurodegenerative disorders. Therefore, investigating cellular pathways by which misfolded proteins are trafficked and cleared ("protein quality control") is of both mechanistic and therapeutic importance. The clearance of most misfolded proteins involves the covalent attachment of one or more ubiquitin molecules; however, the precise fate of the ubiquitinated protein varies greatly, depending on the linkages present in the ubiquitin chain. Here, we discuss approaches for quantifying linkage-specific ubiquitination and clearance of misfolded proteins in the budding yeast Saccharomyces cerevisiae-a model organism used extensively for interrogation of protein quality control pathways, but which presents its own unique challenges for cell and molecular biology experiments. We present a fluorescence microscopy-based assay for monitoring the clearance of misfolded protein puncta, a cycloheximide-chase assay for calculating misfolded protein half-life, and two antibody-based methods for quantifying specific ubiquitin linkages on tagged misfolded proteins, including a 96-well plate-based ELISA. We hope these methods will be of use to the protein quality control, protein degradation, and ubiquitin biology communities.

Keywords: Protein degradation; Protein misfolding; Protein quality control; Protein ubiquitination; Proteostasis; Ubiquitin linkages.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Enzyme-Linked Immunosorbent Assay / methods
  • Humans
  • Microscopy, Fluorescence / methods
  • Protein Folding*
  • Proteolysis*
  • Proteostasis
  • Proteostasis Deficiencies / metabolism
  • Saccharomyces cerevisiae / metabolism
  • Saccharomyces cerevisiae Proteins / metabolism
  • Ubiquitination*

Substances

  • Saccharomyces cerevisiae Proteins