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来源于鸦胆子的天然产物鸦胆子素A作为一种潜在的低密度脂蛋白受体抑制剂,具有促进抗病毒作用。

Natural Product Bruceine A from as a Potential LDLR Inhibitor That Facilitates Antiviral Effect.

作者信息

Zuo Kaiyue, Liu Naiyu, Zhou Peng, Wei Yingrui, Lin Jian, Zhu Xinjie

机构信息

Key Laboratory of Tropical Biological Resources of Ministry of Education, School of Pharmaceutical Sciences, Hainan University, Haikou 570228, China.

Li Song's Academician Workstation of Hainan University (School of Pharmaceutical Sciences), Hainan University, Sanya 572000, China.

出版信息

ACS Omega. 2025 Jun 24;10(26):28210-28219. doi: 10.1021/acsomega.5c02956. eCollection 2025 Jul 8.

Abstract

Low-density lipoprotein receptor (LDLR), which serves as one of the most major entry receptors for many viruses in both human and mouse cells, plays a vital role in virus infection. However, there are no effective small molecules available to inhibit LDLR expression and exhibit antiviral effects. Here, we screened Bruceine A (BA), a natural product derived from the major constituents in which inhibited vesicular stomatitis virus (VSV) infection . Mechanistically, BA blocked viral adsorption and internalization, facilitating antiviral effects through lysosome-mediated degradation of LDLR. Genetic knockdown of exhibited strong antiviral effects. To the best of our knowledge, BA is the first LDLR-selective inhibitor, and our findings reveal that BA may serve as a potent and broad-spectrum virus entry inhibitor based on LDLR entry receptor.

摘要

低密度脂蛋白受体(LDLR)是人类和小鼠细胞中许多病毒最重要的进入受体之一,在病毒感染中起着至关重要的作用。然而,目前尚无有效的小分子可抑制LDLR表达并发挥抗病毒作用。在此,我们筛选了鸦胆子苦醇(BA),一种从主要成分中提取的天然产物,它可抑制水疱性口炎病毒(VSV)感染。从机制上讲,BA阻断病毒吸附和内化,通过溶酶体介导的LDLR降解促进抗病毒作用。LDLR的基因敲低显示出强大的抗病毒作用。据我们所知,BA是首个LDLR选择性抑制剂,我们的研究结果表明,基于LDLR进入受体,BA可能作为一种强效的广谱病毒进入抑制剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f98/12242671/94ff052a4277/ao5c02956_0001.jpg

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