Department of Structural Biology, Van Andel Institute, Grand Rapids, Michigan, USA.
J Biol Chem. 2024 Jun;300(6):107387. doi: 10.1016/j.jbc.2024.107387. Epub 2024 May 17.
The cryo-EM resolution revolution has heralded a new era in our understanding of eukaryotic lipid flippases with a rapidly growing number of high-resolution structures. Flippases belong to the P4 family of ATPases (type IV P-type ATPases) that largely follow the reaction cycle proposed for the more extensively studied cation-transporting P-type ATPases. However, unlike the canonical P-type ATPases, no flippase cargos are transported in the phosphorylation half-reaction. Instead of being released into the intracellular or extracellular milieu, lipid cargos are transported to their destination at the inner leaflet of the membrane. Recent flippase structures have revealed multiple conformational states during the lipid transport cycle. Nonetheless, critical conformational states capturing the lipid cargo "in transit" are still missing. In this review, we highlight the amazing structural advances of these lipid transporters, discuss various perspectives on catalytic and regulatory mechanisms in the literature, and shed light on future directions in further deciphering the detailed molecular mechanisms of lipid flipping.
冷冻电镜分辨率革命预示着我们对真核脂翻转酶的理解进入了一个新时代,越来越多的高分辨率结构被揭示。翻转酶属于 P4 家族的 ATP 酶(IV 型 P 型 ATP 酶),它们在很大程度上遵循了更为广泛研究的阳离子转运 P 型 ATP 酶所提出的反应循环。然而,与典型的 P 型 ATP 酶不同,翻转酶的货物在磷酸化半反应中并没有被转运。脂货物不是被释放到细胞内或细胞外环境中,而是被转运到膜的内层的目的地。最近的翻转酶结构揭示了脂质转运循环过程中的多种构象状态。然而,仍然缺少捕获脂质货物“运输中”的关键构象状态。在这篇综述中,我们强调了这些脂质转运蛋白令人惊叹的结构进展,讨论了文献中关于催化和调节机制的各种观点,并为进一步阐明脂质翻转的详细分子机制指明了未来的方向。