Institute of Biology and Medical Science, Soochow University, Suzhou, Jiangsu, 215123, China.
Anhui Anlong Gene Technology Co., Ltd, Hefei, 230041, China.
Cell Mol Immunol. 2021 Apr;18(4):878-888. doi: 10.1038/s41423-021-00663-2. Epub 2021 Mar 17.
Protein N-myristoylation is an important fatty acylation catalyzed by N-myristoyltransferases (NMTs), which are ubiquitous enzymes in eukaryotes. Specifically, attachment of a myristoyl group is vital for proteins participating in various biological functions, including signal transduction, cellular localization, and oncogenesis. Recent studies have revealed unexpected mechanisms indicating that protein N-myristoylation is involved in host defense against microbial and viral infections. In this review, we describe the current understanding of protein N-myristoylation (mainly focusing on myristoyl switches) and summarize its crucial roles in regulating innate immune responses, including TLR4-dependent inflammatory responses and demyristoylation-induced innate immunosuppression during Shigella flexneri infection. Furthermore, we examine the role of myristoylation in viral assembly, intracellular host interactions, and viral spread during human immunodeficiency virus-1 (HIV-1) infection. Deeper insight into the relationship between protein N-myristoylation and innate immunity might enable us to clarify the pathogenesis of certain infectious diseases and better harness protein N-myristoylation for new therapeutics.
蛋白质 N-豆蔻酰化是由 N-豆蔻酰转移酶(NMTs)催化的重要脂肪酸酰化反应,NMTs 是真核生物中普遍存在的酶。具体来说,豆蔻酰基的附着对于参与各种生物功能的蛋白质至关重要,包括信号转导、细胞定位和致癌作用。最近的研究揭示了出人意料的机制,表明蛋白质 N-豆蔻酰化参与宿主抵抗微生物和病毒感染的防御。在这篇综述中,我们描述了目前对蛋白质 N-豆蔻酰化(主要集中在豆蔻酰开关)的理解,并总结了其在调节先天免疫反应中的关键作用,包括 TLR4 依赖性炎症反应和志贺氏菌感染期间脱豆蔻酰诱导的先天免疫抑制。此外,我们还研究了豆蔻酰化在人类免疫缺陷病毒-1(HIV-1)感染期间病毒组装、细胞内宿主相互作用和病毒传播中的作用。深入了解蛋白质 N-豆蔻酰化与先天免疫之间的关系,可能使我们能够阐明某些传染病的发病机制,并更好地利用蛋白质 N-豆蔻酰化来开发新的治疗方法。