Rapid purification of brain protein complexes containing active and inactive forms of the G protein Gαo
Gαo is the alpha subunit of the most abundant heterotrimeric G protein of the brain and relays signals from G protein-coupled receptors to inhibit neural function. To date, no direct downstream effectors for Gαo have been well-characterized. Active Gα-GTP proteins should form stable complexes with their effectors, but identifying Gαo effectors by isolating such complexes is a challenge since the vast majority of Gαo in the brain is in its inactive, GDP-bound form. In this study, we developed methods to isolate microgram quantities of native Gαo-GTP protein complexes by immunoprecipitation from brain lysates. We found that native Gαo protein in crude detergent lysates of mouse brain rapidly binds and is activated by the slowly-hydrolyzable GTP analog GTPγS. Using size exclusion chromatography and tracking the Gαo-containing complexes by western blotting, we found that native Gαo in crude brain lysates exists in complexes that change size upon activation by GTPγS. We also identified a monoclonal antibody that can efficiently immunoprecipitate Gαo protein complexes from mouse brain lysates for downstream applications such as mass spectrometry and protein-protein interaction assays. Our results and methods enable further research into the Gαo signaling pathway.
Authors
- Suresh Yadav (ORCID: https://orcid.org/0009-0006-2200-3589)
- Michael R. Koelle (ORCID: https://orcid.org/0000-0001-9486-8481)
- Santosh Kumar (ORCID: https://orcid.org/0000-0002-9363-3530)
- S. Meena
- Satya Santoshi Veliventi
Institutions
- Yale University (US)
- Regional Centre for Biotechnology (IN)
- National Centre for Cell Science (IN)
- Acceleron Pharma (United States) (US)
- UCB Pharma (United States) (US)
- Savitribai Phule Pune University (IN)
Publication Details
- Journal
- PLoS ONE
- Published
- 2025-12-04
- DOI
- https://doi.org/10.1371/journal.pone.0337998
- Primary Topic
- Protein Kinase Regulation and GTPase Signaling
- Type
- article
- Field-Weighted Citation Impact
- 0.00