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<p>Chemokine receptors CXCR4 and ACKR3 are involved in multiple physiological and pathological processes. In overexpression systems, CXCR4 and ACKR3 form oligomers that are important for chemokine recognition and signaling. Whether this holds true in physiological settings is unknown as no evidence of such oligomers are available. To address this gap of knowledge, we develop a new approach for GPCR oligomer detection by time-resolved Förster resonance energy transfer (TR-FRET) between fluorescently labeled nanobodies. Fluorescent probes are conjugated to the C-terminus of extracellularly binding nanobodies using site-directed sortase-mediated labeling, retaining high affinity of the nanobodies for their target receptors. This approach, first validated in transfected cells by detecting the presence of CXCR4 and ACKR3 homo-oligomers and hetero-oligomers, reveals for the first time endogenous CXCR4 homo-oligomers in non-transfected human leukemia/lymphoma-derived cancer cell lines. More importantly, the investigation in peripheral blood mononuclear cells strongly supports the existence of CXCR4 oligomers in native conditions.</p>

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TR-FRET between engineered nanobodies reveals the existence of endogenous CXCR4 oligomers

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2025年12月16日

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  • Joyce Heuninck,
  • Vladimir Bobkov,
  • Claire M. Grison,
  • Amos Fumagalli,
  • Mathias Lescuyer,
  • Omolade Otun,
  • Cherine Bechara,
  • Laurent Lamarque,
  • Eric Trinquet,
  • Françoise Bachelerie,
  • Philippe Marin,
  • Bernard Mouillac,
  • Sébastien Granier,
  • Bas van der Woning,
  • Hans de Haard,
  • Martine J. Smit,
  • Raimond Heukers,
  • Thierry Durroux

摘要

Chemokine receptors CXCR4 and ACKR3 are involved in multiple physiological and pathological processes. In overexpression systems, CXCR4 and ACKR3 form oligomers that are important for chemokine recognition and signaling. Whether this holds true in physiological settings is unknown as no evidence of such oligomers are available. To address this gap of knowledge, we develop a new approach for GPCR oligomer detection by time-resolved Förster resonance energy transfer (TR-FRET) between fluorescently labeled nanobodies. Fluorescent probes are conjugated to the C-terminus of extracellularly binding nanobodies using site-directed sortase-mediated labeling, retaining high affinity of the nanobodies for their target receptors. This approach, first validated in transfected cells by detecting the presence of CXCR4 and ACKR3 homo-oligomers and hetero-oligomers, reveals for the first time endogenous CXCR4 homo-oligomers in non-transfected human leukemia/lymphoma-derived cancer cell lines. More importantly, the investigation in peripheral blood mononuclear cells strongly supports the existence of CXCR4 oligomers in native conditions.