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Multivalent, ligand-directed molecular beacons undergo conformational switching at the cell surface, enabling fluorescence turn-on detection of membrane receptors. In the Research Article e3191334, David Margulies and co-workers reported the modular design of these probes enables tunable receptor selectivity, binding affinity, and emission properties, providing a versatile platform for wash-free receptor imaging, detecting receptor–inhibitor interactions, and evaluating therapeutic antibodies.
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Oppenheimer‐Low et al. (2026) studied this question.
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