FRET imaging reveals that functional neurokinin-1 receptors are monomeric and reside in membrane microdomains of live cells

TLDR

The study used FRET microscopy with ACP labeling to examine the lateral organization of neurokinin‑1 receptors in living cells. NK1Rs were expressed as ACP fusion proteins, covalently labeled with fluorophores, enabling high‑signal‑to‑noise FRET imaging with controlled donor‑acceptor ratios and surface‑specific labeling for precise quantification. Single‑cell FRET data showed NK1Rs remain monomeric, with FRET intensity scaling with receptor density, revealing clustering in ~1 % of the membrane microdomains that are disrupted by cholesterol depletion.

Abstract

The lateral organization of a prototypical G protein-coupled receptor, the neurokinin-1 receptor (NK1R), was investigated in living cells by fluorescence resonance energy transfer (FRET) microscopy, taking advantage of the recently developed acyl carrier protein (ACP) labeling technique. The NK1R was expressed as fusion protein with ACP to which small fluorophores were then covalently bound. Our approach allowed the recording of FRET images of receptors on living cells with unprecedented high signal-to-noise ratios and a subsequent unequivocal quantification of the FRET data owing to ( i ) the free choice of optimal fluorophores, ( ii ) the labeling of NK1Rs exclusively on the cell surface, and ( iii ) the precise control of the donor–acceptor molar ratio. Our single-cell FRET measurements exclude the presence of constitutive or ligand-induced homodimers or oligomers of NK1Rs. The strong dependence of FRET on the receptor concentration further reveals that NK1Rs tend to concentrate in microdomains, which are found to constitute ≈1% of the cell membrane and to be sensitive to cholesterol depletion.