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APEX2-Mediated Proximity Protein Labeling in Dictyostelium.
- Source :
-
Methods in molecular biology (Clifton, N.J.) [Methods Mol Biol] 2024; Vol. 2814, pp. 119-131. - Publication Year :
- 2024
-
Abstract
- Largely due to its simplicity, while being more like human cells compared to other experimental models, Dictyostelium continues to be of great use to discover basic molecular mechanisms and signaling pathways underlying evolutionarily conserved biological processes. However, the identification of new protein interactions implicated in signaling pathways can be particularly challenging in Dictyostelium due to its extremely fast signaling kinetics coupled with the dynamic nature of signaling protein interactions. Recently, the proximity labeling method using engineered ascorbic acid peroxidase 2 (APEX2) in mammalian cells was shown to allow the detection of weak and/or transient protein interactions and also to obtain spatial and temporal resolution. Here, we describe a protocol for successfully using the APEX2-proximity labeling method in Dictyostelium. Coupled with the identification of the labeled proteins by mass spectrometry, this method expands Dictyostelium's proteomics toolbox and should be widely useful for identifying interacting partners involved in a variety of biological processes in Dictyostelium.<br /> (© 2024. The Editor(s) (if applicable) and The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature.)
- Subjects :
- Protein Interaction Mapping methods
Mass Spectrometry methods
Protozoan Proteins metabolism
Protozoan Proteins genetics
Humans
DNA-(Apurinic or Apyrimidinic Site) Lyase metabolism
Signal Transduction
Staining and Labeling methods
Endonucleases
Multifunctional Enzymes
Dictyostelium metabolism
Ascorbate Peroxidases metabolism
Ascorbate Peroxidases genetics
Proteomics methods
Subjects
Details
- Language :
- English
- ISSN :
- 1940-6029
- Volume :
- 2814
- Database :
- MEDLINE
- Journal :
- Methods in molecular biology (Clifton, N.J.)
- Publication Type :
- Academic Journal
- Accession number :
- 38954202
- Full Text :
- https://doi.org/10.1007/978-1-0716-3894-1_9