Department of Biochemistry, University of Toronto, Toronto, ON M5S 1A8, Canada.
Pharmaceutical Sciences, University of Illinois Chicago, Chicago, IL 60612, USA.
Biomolecules. 2023 Jul 14;13(7):1130. doi: 10.3390/biom13071130.
Viral entry and fertilization are distinct biological processes that share a common mechanism: membrane fusion. In viral entry, enveloped viruses attach to the host cell membrane, triggering a series of conformational changes in the viral fusion proteins. This results in the exposure of a hydrophobic fusion peptide, which inserts into the host membrane and brings the viral and host membranes into close proximity. Subsequent structural rearrangements in opposing membranes lead to their fusion. Similarly, membrane fusion occurs when gametes merge during the fertilization process, though the exact mechanism remains unclear. Structural biology has played a pivotal role in elucidating the molecular mechanisms underlying membrane fusion. High-resolution structures of the viral and fertilization fusion-related proteins have provided valuable insights into the conformational changes that occur during this process. Understanding these mechanisms at a molecular level is essential for the development of antiviral therapeutics and tools to influence fertility. In this review, we will highlight the biological importance of membrane fusion and how protein structures have helped visualize both common elements and subtle divergences in the mechanisms behind fusion; in addition, we will examine the new tools that recent advances in structural biology provide researchers interested in a frame-by-frame understanding of membrane fusion.
病毒进入和受精是两个截然不同的生物学过程,但它们共享一个共同的机制:膜融合。在病毒进入过程中,包膜病毒附着在宿主细胞膜上,触发病毒融合蛋白的一系列构象变化。这导致疏水性融合肽暴露,插入宿主膜并使病毒和宿主膜紧密接近。随后,在相反的膜中发生结构重排,导致它们融合。同样,当配子在受精过程中融合时,也会发生膜融合,尽管确切的机制尚不清楚。结构生物学在阐明膜融合的分子机制方面发挥了关键作用。病毒和受精融合相关蛋白的高分辨率结构提供了宝贵的见解,了解了这个过程中发生的构象变化。在分子水平上理解这些机制对于开发抗病毒治疗药物和影响生育力的工具至关重要。在这篇综述中,我们将强调膜融合的生物学重要性,以及蛋白质结构如何帮助我们可视化融合机制背后的共同元素和细微差异;此外,我们还将研究结构生物学的最新进展为有兴趣从框架到框架理解膜融合的研究人员提供的新工具。