Hou Dan, Zheng Chunfu, Yu Tao
Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Department of Microbiology, Immunology & Infectious Diseases, University of Calgary, Calgary, AB, Canada.
Methods Mol Biol. 2025;2940:1-9. doi: 10.1007/978-1-0716-4615-1_1.
Fatty acylation has a critical impact on antiviral innate immunity. Fatty acylation of virus proteins affects virus virulence and invasion. In contrast, fatty acylation of host cell proteins regulates virus recognition and host-virus interactions, thus affecting antiviral immune responses. Therefore, an emerging need exists to investigate and understand the mechanism and function of protein fatty acylation in regulating antiviral innate immunity. Alkyne probe metabolic labeling and click chemistry assays with biotin-conjugated or fluorophore-conjugated azide provide a simple way to determine the potential fatty-acylated proteins in antiviral innate pathways. Here, we demonstrate comprehensive approaches to determine protein fatty acylation in virus-infected macrophages or protein-overexpressing HEK293T cells in the context of antiviral innate immunity.
脂肪酰化对抗病毒天然免疫具有关键影响。病毒蛋白的脂肪酰化会影响病毒毒力和侵袭。相反,宿主细胞蛋白的脂肪酰化调节病毒识别以及宿主 - 病毒相互作用,从而影响抗病毒免疫反应。因此,迫切需要研究和了解蛋白质脂肪酰化在调节抗病毒天然免疫中的机制和功能。炔烃探针代谢标记以及与生物素偶联或荧光团偶联叠氮化物的点击化学分析,为确定抗病毒天然免疫途径中潜在的脂肪酰化蛋白提供了一种简单方法。在此,我们展示了在抗病毒天然免疫背景下,用于确定病毒感染的巨噬细胞或过表达蛋白的HEK293T细胞中蛋白质脂肪酰化的综合方法。