LvID 对大鼠 α7 尼古丁乙酰胆碱受体的选择性抑制作用,LvID 是一种新发现的芋螺α4/7-神经毒素

IF 7.3 1区 医学 Q1 CHEMISTRY, MEDICINAL Journal of Medicinal Chemistry Pub Date : 2025-04-09 DOI:10.1021/acs.jmedchem.4c02810
Man Guo, Xiaopeng Zhu, Tao Ma, Chenxing Xu, Dongting Zhangsun, Jinpeng Yu, Quentin Kaas, Peta J. Harvey, J. Michael McIntosh, David J. Craik, Sulan Luo
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引用次数: 0

摘要

α7烟碱乙酰胆碱受体(nachr)存在于外周和中枢神经系统中,对认知功能、记忆、炎症至关重要,并与阿尔茨海默病(AD)、肺癌、重症肌无力和动脉粥样硬化等疾病有关。本文报道了一种新的α4/7-conotoxin (CTx) LvID,该LvID可以有效抑制爪蟾卵母细胞中表达的大鼠α7 nAChR, IC50为13.8 nM,而对其他大鼠nAChR亚型的抑制作用很小。LvID的结构经核磁共振(NMR)鉴定为由二硫键支撑的短螺旋结构。从一系列丙氨酸突变体中确定了LvID与α7 nachr结合的关键残基。分子模拟为LvID结合α7 nAChRs的活性和特异性提供了可能的解释。这一发现为研究α7 nachr的结构特征和功能机制提供了重要的药理学工具。
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Selective Inhibition of Rat α7 Nicotinic Acetylcholine Receptors by LvID, a Newly Characterized α4/7-Conotoxin from Conus lividus
The α7 nicotinic acetylcholine receptors (nAChRs), identified in peripheral and central nervous systems, are crucial for cognitive function, memory, inflammation, and are linked to disorders like Alzheimer’s disease (AD), lung cancer, myasthenia gravis, and atherosclerosis. Here we report that a novel α4/7-conotoxin (CTx) LvID, from Conus lividus, potently inhibits rat α7 nAChRs expressed in Xenopus oocytes with an IC50 of 13.8 nM, showing little activity against other rat nAChR subtypes. The structure of LvID was elucidated using nuclear magnetic resonance (NMR) spectroscopy and comprises a short helix braced by disulfide bonds. The key residues of LvID that bind to the α7 nAChRs were determined from a series of alanine mutants. Molecular simulation provided a possible explanation for the activity and specificity of LvID binding to α7 nAChRs. This finding offers a vital pharmacological tool for investigating the structural features and functional mechanisms of α7 nAChRs.
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来源期刊
Journal of Medicinal Chemistry
Journal of Medicinal Chemistry 医学-医药化学
CiteScore
4.00
自引率
11.00%
发文量
804
审稿时长
1.9 months
期刊介绍: The Journal of Medicinal Chemistry is a prestigious biweekly peer-reviewed publication that focuses on the multifaceted field of medicinal chemistry. Since its inception in 1959 as the Journal of Medicinal and Pharmaceutical Chemistry, it has evolved to become a cornerstone in the dissemination of research findings related to the design, synthesis, and development of therapeutic agents. The Journal of Medicinal Chemistry is recognized for its significant impact in the scientific community, as evidenced by its 2022 impact factor of 7.3. This metric reflects the journal's influence and the importance of its content in shaping the future of drug discovery and development. The journal serves as a vital resource for chemists, pharmacologists, and other researchers interested in the molecular mechanisms of drug action and the optimization of therapeutic compounds.
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