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<p>GPCR therapeutics primarily target structured cavities formed by the seven transmembrane α-helices. However, amino acid sequence conservation in structured regions, especially among receptor subtypes, limits target selectivity. Here, we leverage the sequence divergence of the third intracellular loop (ICL3) of the receptor fold to derive a selective positive allosteric modulator for the β<sub>2</sub> adrenergic receptor (β<sub>2</sub>AR). We repurpose the variable regions of a previously reported monoclonal antibody (Mab5) as single-chain (ScFv5) and single-domain (VhhL5) antibody fragments that enhance the maximal second messenger cyclic AMP signaling response downstream of the receptor. Despite ScFv5 binding a segment of ICL3 distinct to β<sub>2</sub>AR, it also non-selectively binds and modulates cAMP signaling downstream of β<sub>1</sub>AR and β<sub>3</sub>AR. We find that this lack of specificity stems from multiple redundant interactions that facilitate ScFv5-ICL3 binding. In contrast, VhhL5, derived from the Mab5 light chain, selectively modulates β<sub>2</sub>AR signaling over the β<sub>1</sub>/β<sub>3</sub> subtypes. Mechanistically, VhhL5 enhances agonist-stimulated β<sub>2</sub>AR-G protein coupling through releasing autoinhibitory ICL3 conformational states. In parallel, VhhL5 decreases β<sub>2</sub>AR internalization promoting greater ligand-induced accumulation of cAMP. Our study demonstrates proof-of-concept for selective allosteric modulation of a GPCR by targeting a sequence divergent loop region within the receptor fold.</p>

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Selective positive allosteric modulation of β2AR using antibody fragments targeting the third intracellular loop

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2026年5月6日

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  • Edgardo J. Sánchez Rivas,
  • Fredrik Sadler,
  • Mohammadamin Safdari,
  • Nishaben M. Patel,
  • Michael Ritt,
  • Ning Ma,
  • Sergio Branciamore,
  • Nagarajan Vaidehi,
  • Sivaraj Sivaramakrishnan

摘要

GPCR therapeutics primarily target structured cavities formed by the seven transmembrane α-helices. However, amino acid sequence conservation in structured regions, especially among receptor subtypes, limits target selectivity. Here, we leverage the sequence divergence of the third intracellular loop (ICL3) of the receptor fold to derive a selective positive allosteric modulator for the β2 adrenergic receptor (β2AR). We repurpose the variable regions of a previously reported monoclonal antibody (Mab5) as single-chain (ScFv5) and single-domain (VhhL5) antibody fragments that enhance the maximal second messenger cyclic AMP signaling response downstream of the receptor. Despite ScFv5 binding a segment of ICL3 distinct to β2AR, it also non-selectively binds and modulates cAMP signaling downstream of β1AR and β3AR. We find that this lack of specificity stems from multiple redundant interactions that facilitate ScFv5-ICL3 binding. In contrast, VhhL5, derived from the Mab5 light chain, selectively modulates β2AR signaling over the β1/β3 subtypes. Mechanistically, VhhL5 enhances agonist-stimulated β2AR-G protein coupling through releasing autoinhibitory ICL3 conformational states. In parallel, VhhL5 decreases β2AR internalization promoting greater ligand-induced accumulation of cAMP. Our study demonstrates proof-of-concept for selective allosteric modulation of a GPCR by targeting a sequence divergent loop region within the receptor fold.