Authors
Lulu Guo, Weifeng Zhang, Xuan Li, Canyang Niu, Zili Liu, Zaiyu Zhang, Honghao Fan, Xihe Gao, Kaiyu Wang, Haoran Liu, Chunhong Zhang, Ying Li, Ziran Wang, Fan Yang, Guoqiang Li, Jinpeng Sun
Published in
Biosensors & bioelectronics. Volume 312. Pages 119064. Jul 23, 2026. Epub Jul 23, 2026.
Abstract
Biosensors inspired by biological sensory systems are valuable tools for detecting physiological and environmental stimuli with high degrees of specificity and sensitivity. An itch irritant biosensor to detect environmental changes or pruritogenic substances in human blood or tissues highly associated with inflammation and prevalent conditions like atopic dermatitis (AD) has not been developed. To address this gap, we developed a novel bioelectronic sensor by integrating the human itch receptor Mas-related G-protein-coupled receptor X2 (MRGPRX2) with a graphene field-effect transistor (GFET). This MRGPRX2-GFET biosensor covalently immobilizes functional receptors, enabling direct conversion of ligand-binding events into quantifiable electrical signals. We demonstrate that the sensor can detect known MRGPRX2 agonists with exceptional sensitivity and specificity, achieving a detection limit for SP at approximately 7 pM. Molecular dynamics (MD) simulations and mutational effects reveal that ligand binding induces cytoplasmic conformational rearrangements in MRGPRX2, strengthening receptor-graphene coupling and providing a mechanistic basis for signal transduction. Importantly, the biosensor effectively distinguishes plasma samples from AD patients and healthy controls by capturing different electrical signal responses. In our study, we establish a versatile platform for diagnosing and subtyping chronic itch disorders and offer a generalizable strategy for developing membrane receptor-based multiplexed "itch-print" biosensors.
PMID:
42531649
Bibliographic data and abstract were imported from PubMed on 31 Jul 2026.
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