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Fast Identification of In Vivo Protein Phosphorylation Events Using Transient Expression in Leaf Mesophyll Protoplasts and Phos-tag TM SDS-PAGE.

Ellen BrouckeFilip RollandNathalie Crepin
Published in: Methods in molecular biology (Clifton, N.J.) (2023)
Phosphorylation/dephosphorylation is a key posttranslational mechanism for signal transduction and amplification. Several techniques exist for assessing protein phosphorylation status, but each has its own drawbacks. The fast, straightforward, and low-tech approach described here uses transient overexpression of peptide-tagged proteins in Arabidopsis leaf mesophyll protoplasts and immunoblotting with Phos-tag™ SDS-PAGE and commercial anti-tag antibodies. We illustrate this with two relevant examples related to the SnRK1 protein kinase, which mediates metabolic stress signaling: Arabidopsis thaliana SnRK1 activation by T-loop (auto-)phosphorylation and SnRK1 phosphorylation of the Arabidopsis RAV1 transcription factor, which is involved in seed germination and early seedling development.
Keyphrases
  • protein kinase
  • transcription factor
  • arabidopsis thaliana
  • binding protein
  • poor prognosis
  • dna binding
  • protein protein
  • cell proliferation
  • amino acid
  • genome wide identification