Subcellular Fractionation for ERK Activation Upon Mitochondrial-derived Peptide Treatment

J Vis Exp. 2017 Sep 25:(127):56496. doi: 10.3791/56496.

Abstract

Mitochondrial-derived peptides (MDPs) are a new class of peptides that are encoded by small open reading frames within other known genes of the mitochondrial genome. MDPs have a wide variety of biological effects such as protecting neurons from apoptosis, improving metabolic markers, and protecting cells from chemotherapy. Humanin was the first MDP to be discovered and is the most studied peptide among the MDP family. The membrane receptors and downstream signaling pathways of humanin have been carefully characterized. Additional MDPs such as MOTS-c and SHLP1-6 have been more recently discovered and the signaling mechanisms have yet to be elucidated. Here we describe a cell culture based method to determine the function of these peptides. In particular, cell fractionation techniques in combination with western blotting allow for the quantitative determination of activation and translocation of important signaling molecule. While there are other methods of cell fractionation, the one described here is an easy and straightforward method. These methods can be used to further elucidate the mechanism of action of these peptides and other therapeutic agents.

Publication types

  • Video-Audio Media

MeSH terms

  • HEK293 Cells
  • Humans
  • Intracellular Signaling Peptides and Proteins / chemistry
  • Intracellular Signaling Peptides and Proteins / pharmacology
  • MAP Kinase Signaling System / drug effects*
  • Mitochondria / chemistry
  • Mitochondria / enzymology
  • Mitochondria / metabolism*
  • Peptides / metabolism
  • Peptides / pharmacology*
  • Subcellular Fractions / enzymology
  • Subcellular Fractions / metabolism

Substances

  • Intracellular Signaling Peptides and Proteins
  • Peptides
  • humanin