Project Details
Projekt
Peptide-templated bioconjugation of proteins on and in live cells for studies of GPCR trafficking and crosstalk
Subject Area
Biological and Biomimetic Chemistry
Biochemistry
Biochemistry
Term
from 2012 to 2020
Project identifier
Deutsche Forschungsgemeinschaft (DFG) - Project number 223301960
The functional properties of G-protein coupled receptors (GPCRs) depend on localization, density of surface expression and their mobility in the cell membrane. Some GPCRs undergo dynamic equilibria between monomeric and dimeric forms. Microscopic imaging has become an indispensable tool to study fluorescence labelled GPCRs on and in live cells. However, it has to be considered that the fluorescent tag can affect GPCR functional properties such as export to the cell membrane, ligand binding and GPCR internalization. In the previous funding period, we developed a labeling method that requires only small tag sequences, occurs with high tag specificity, proceeds within minutes (rather than hours) and enables the introduction of virtually any reporter group. The labeled receptors maintained their activity and internalized upon stimulation with the ligands. At the current stage our method is restricted to the labeling of extracellular protein regions. It is the aim to develop a protein labeling reaction which sustains the favorable properties (small tag size, modularity) of our method yet i) provides access to intracellular targets (AdipoR1 receptor, arrestins, regulators of G-protein signaling proteins), ii) makes available multiplexed protein imaging (via multiplexed peptide-directed acyl transfer), iii) enables live cell quantification of expression (via live cell rolling circle amplification after labeling of GPCR with PNA) and iv) allows for control over the oligomerization state of GPCRs (via hybridization of PNA-labeled GPCRs with DNA/PNA).The methods developed in the joined research project will allow us to investigate the dynamics of human Y, NPFF, CRF and ghrelin receptors. We will analyze receptor crosstalk, quantify the receptors accessible by the ligand and elucidate the intracellular pathways and interaction partners in a dynamic (by FRET) or time-resolved (by pulse-chase experiments) manner. Furthermore we will expand the concept to other tags, create semi-synthetic receptors (e. g. in vivo lipidated or pegylated receptor constructs) for studying their function.
DFG Programme
Priority Programmes
