posted on 2025-03-27, 15:17authored byAshley
N. Ives, Kevin Jooß, Rafael D. Melani, Ryan T. Fellers, John Janetzko, Neil L. Kelleher
G protein-coupled
receptors (GPCRs) are the largest class of integral
membrane receptors and responsible for transmitting diverse signals
in response to extracellular stimuli. Post-translational modifications
serve to dictate the subcellular trafficking and function of a GPCR
across space and time. Despite significant interest in mapping the
diversity of GPCR modification states (proteoforms), technical challenges
have hindered this characterization. While advancements in membrane
mimetics and mass spectrometry instrumentation have improved analysis,
current workflows require large amounts of homogeneous protein, limiting
the study of many GPCRs from mammalian sources. Here, we present capillary
zone electrophoresis (CZE) as a separation technique for characterizing
proteoforms of both intact and partially digested GPCRs. This method
allowed for the characterization of multiple proteoforms of both the
β2-adrenergic receptor and metabotropic glutamate receptor 2
using low sample volumes and without buffer optimization. Notably,
in the case of smaller phosphorylated analytes, CZE can readily separate
positional phosphorylation isomers and provide superior fragmentation
coverage to conventional reversed phase-liquid chromatography.