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Pupylation-Based Proximity-Tagging of FERONIA-Interacting Proteins in Arabidopsis.
- Source :
-
Molecular & cellular proteomics : MCP [Mol Cell Proteomics] 2024 Nov; Vol. 23 (11), pp. 100828. Date of Electronic Publication: 2024 Aug 13. - Publication Year :
- 2024
-
Abstract
- The plasma membrane-localized receptor kinase FERONIA (FER) plays critical roles in a remarkable variety of biological processes throughout the life cycle of Arabidopsis thaliana. Revealing the molecular connections of FER that underlie these processes starts with identifying the proteins that interact with FER. We applied pupylation-based interaction tagging (PUP-IT) to survey cellular proteins in proximity to FER, encompassing weak and transient interactions that can be difficult to capture for membrane proteins. We reproducibly identified 581, 115, and 736 specific FER-interacting protein candidates in protoplasts, seedlings, and flowers, respectively. We also confirmed 14 previously characterized FER-interacting proteins. Protoplast transient gene expression expedited the testing of new gene constructs for PUP-IT analyses and the validation of candidate proteins. We verified the proximity labeling of five selected candidates that were not previously characterized as FER-interacting proteins. The PUP-IT method could be a valuable tool to survey and validate protein-protein interactions for targets of interest in diverse subcellular compartments in plants.<br />Competing Interests: Conflict of interest The authors declare that they have no conflict of interest with the contents of this article.<br /> (Copyright © 2024 The Authors. Published by Elsevier Inc. All rights reserved.)
- Subjects :
- Flowers metabolism
Flowers genetics
Phosphotransferases metabolism
Protoplasts metabolism
Protein Interaction Mapping methods
Seedlings metabolism
Seedlings genetics
Protein Binding
Protein Serine-Threonine Kinases
Arabidopsis metabolism
Arabidopsis genetics
Arabidopsis Proteins metabolism
Arabidopsis Proteins genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1535-9484
- Volume :
- 23
- Issue :
- 11
- Database :
- MEDLINE
- Journal :
- Molecular & cellular proteomics : MCP
- Publication Type :
- Academic Journal
- Accession number :
- 39147029
- Full Text :
- https://doi.org/10.1016/j.mcpro.2024.100828