Optimized protocol for the identification of lipid droplet proteomes using proximity labeling proteomics in cultured human cells

STAR Protoc. 2021 Jun 5;2(2):100579. doi: 10.1016/j.xpro.2021.100579. eCollection 2021 Jun 18.

Abstract

Lipid droplets are endoplasmic reticulum-derived neutral lipid storage organelles that play critical roles in cellular lipid and energy homeostasis. Here, we present a protocol for the identification of high-confidence lipid droplet proteomes in a cell culture model. This approach overcomes limitations associated with standard biochemical fractionation techniques, employing an engineered ascorbate peroxidase (APEX2) to biotinylate endogenous lipid droplet proteins in living cells for subsequent purification and identification by proteomics. For complete details on the use and execution of this protocol, please refer to Bersuker et al. (2018).

Keywords: Cell Biology; Cell Membrane; Cell culture; Cell separation/fractionation; Cell-based Assays; Proteomics.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Ascorbate Peroxidases / metabolism
  • Biotin / metabolism
  • Cells, Cultured
  • DNA-(Apurinic or Apyrimidinic Site) Lyase / metabolism
  • Endonucleases / metabolism
  • Endoplasmic Reticulum / metabolism
  • Humans
  • Lipid Droplets / metabolism*
  • Multifunctional Enzymes / metabolism
  • Proteome*

Substances

  • Multifunctional Enzymes
  • Proteome
  • Biotin
  • Ascorbate Peroxidases
  • Endonucleases
  • APEX2 protein, human
  • DNA-(Apurinic or Apyrimidinic Site) Lyase