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Construction and function of nicotinic acetylcholine receptor α6/α3β2β3 mutants
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Ze-pei TANG, Xuan ZHOU, Bai-xue AN, Jin-peng YU, Su-lan LUO*, Dong-ting ZHANGSUN*
Acta Pharmaceutica Sinica | 2026, 61(1) : 184 - 193
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Acta Pharmaceutica Sinica | 2026, 61(1): 184-193
• Original Articles •
Construction and function of nicotinic acetylcholine receptor α6/α3β2β3 mutants
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Ze-pei TANG, Xuan ZHOU, Bai-xue AN, Jin-peng YU, Su-lan LUO*, Dong-ting ZHANGSUN*
Affiliations
  • Guangxi Key Laboratory of Special Biomedicine, School of Medicine, Guangxi University, Nanning 530004, China
Published: 2026-01-12 doi: 10.16438/j.0513-4870.2025-0693
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α6/α3β2β3 nicotinic acetylcholine receptors (nAChRs) subtype is widely expressed in mesolimbic dopaminergic pathway and other regions, which plays a vital role in modulating the release of multiple neurotransmitters and drug reward mechanisms. It has become a potential therapeutic target for the treatment of various neuropsychiatric disorders and drug addiction. However, most ligands identified with high affinity and selectivity targeting α6/α3β2β3 subtype showed limited subtype discrimination against the closely related α3β2 subtype. Furthermore, the molecular mechanisms underlying ligands interact with α6/α3β2β3 nAChR remain absent. In this study, the related approaches of site-directed mutagenesis of receptor, in vitro transcription and electrophysiological assay were utilized to establish the drug screening models of wild-type α6/α3β2β3 nAChR and its α6/α3 subunit single-point mutants. The effects led by single amino acid substitution to the function of α6/α3β2β3 nAChR were also evaluated. The animal experimental protocol involved in this study has been approved by the Ethics Committee of Guangxi University (Approval No: GXU-2023-0249). As the results showed, the half maximal effective concentration (EC50) for ACh activating α6/α3β2β3 nAChR was 18.5 μmol·L-1. All 7 single-point mutations of α6/α3 subunit resulted in increase of the agonist sensitivity, while the EC50 of ACh towards mutants α6/α3[V112E]β2β3、α6/α3[T147S]β2β3、α6/α3[E152K]β2β3 nAChR decreased to the greatest extent (EC50s were 3.5, 4.4, and 2.0 μmol·L-1, respectively, which were 0.1-0.2-fold relative to that of the wild-type receptor). These results established models for the research of structure-function relationship of α6/α3β2β3 nAChRs and molecular mechanism of ligand-receptor specific binding, as well as provided theoretical foundation for the design and optimization of selective drug leads targeting α6/α3β2β3 nAChRs.

α6/α3β2β3 nicotinic acetylcholine receptor  /  PCR-mediated site-directed mutagenesis  /  two-electrode voltage clamp technique  /  Xenopus oocyte  /  half-maximal excitatory concentration
唐则佩, 周煊, 安佰雪, 于津鹏, 罗素兰, 长孙东亭. 烟碱型乙酰胆碱受体α6/α3β2β3突变型的构建及其功能研究. 药学学报, 2026 , 61 (1) : 184 -193 . DOI: 10.16438/j.0513-4870.2025-0693
Ze-pei TANG, Xuan ZHOU, Bai-xue AN, Jin-peng YU, Su-lan LUO, Dong-ting ZHANGSUN. Construction and function of nicotinic acetylcholine receptor α6/α3β2β3 mutants[J]. Acta Pharmaceutica Sinica, 2026 , 61 (1) : 184 -193 . DOI: 10.16438/j.0513-4870.2025-0693
Year 2026 volume 61 Issue 1
165
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doi: 10.16438/j.0513-4870.2025-0693
  • Receive Date:2025-06-18
  • Online Date:2026-09-21
  • Published:2026-01-12
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  • Received:2025-06-18
  • Revised:2025-08-30
Affiliations
    Guangxi Key Laboratory of Special Biomedicine, School of Medicine, Guangxi University, Nanning 530004, China
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表12种不同金属材料的力学参数
科
Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)
属
Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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