Yeasmin Sabina, Sharma Kavita, Nicolet Christopher, DeCristofano Laura, Ataian Yeganeh, Ranjit Arina, Aghazadeh-Habashi Ali, Xu Dong, Schulte Marvin
Department of Biomedical and Pharmaceutical Sciences, Idaho State University, Pocatello, ID, 83209, USA.
Department of Pharmaceutical Sciences, Saint Joseph's University, 600 South 43rd Street, Philadelphia, PA, 19104, USA.
Npj Viruses. 2025 Jun 24;3(1):52. doi: 10.1038/s44298-025-00109-w.
Herpes virus1(HSV1) is a neurotropic virus that has been linked to Alzheimer's disease. An In-silico structural homology search using α -Bgtx, identified structural homology between HSV1 gD and the nicotinic receptor neurotoxin α-Bgtx. SPR binding studies using acetylcholine binding protein from Lymnaea stagnalis, and functional two electrode voltage clamp studies of α7 nAChRs demonstrate the ability of HSV1 to interact directly with nAChRs. Molecular docking studies support the binding of a neurotoxin-like binding loop in HSV1 to a binding site similar to the neurotoxin binding domain. Interaction of HSV1 with nAChRs provides novel insights into a potential mechanism of action of HSV and its potential role in Alzheimer's disease.
单纯疱疹病毒1型(HSV1)是一种嗜神经病毒,与阿尔茨海默病有关。使用α -银环蛇毒素进行的计算机模拟结构同源性搜索,确定了HSV1 gD与烟碱样受体神经毒素α -银环蛇毒素之间的结构同源性。使用椎实螺乙酰胆碱结合蛋白进行的表面等离子体共振结合研究,以及对α7烟碱型乙酰胆碱受体的功能性双电极电压钳研究,证明了HSV1与烟碱型乙酰胆碱受体直接相互作用的能力。分子对接研究支持HSV1中一个神经毒素样结合环与一个类似于神经毒素结合域的结合位点的结合。HSV1与烟碱型乙酰胆碱受体的相互作用为HSV的潜在作用机制及其在阿尔茨海默病中的潜在作用提供了新的见解。