人类abca7介导的脂质转运的结构见解

IF 4.4 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Structure Pub Date : 2025-01-17 DOI:10.1016/j.str.2024.12.015
Shu-Cheng Fang, Liang Wang, Meng-Ting Cheng, Da Xu, Zhi-Peng Chen, Jie Wang, Wenli Liao, Yanyan Li, Cong-Zhao Zhou, Wen-Tao Hou, Yuxing Chen
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引用次数: 0

摘要

人类 ATP 结合盒(ABC)转运体 ABCA7 参与脂蛋白载脂蛋白的脂化,而脂蛋白载脂蛋白是公认的阿尔茨海默病(AD)风险因素。人们对ABCA7如何参与阿尔茨海默病的分子发病机制仍知之甚少。我们利用冷冻电子显微镜(cryo-EM)分别测定了ABCA7的载脂蛋白和底物结合型结构。结合活性测定,我们确定了以 "尾对尾 "方式特异性结合两分子磷脂酰丝氨酸(PS)的残基。下拉实验证实载脂蛋白与 ABCA7 直接相互作用;此外,在载脂蛋白存在的情况下,ABCA7 的 ATPase 和脂质转运活性都显著增强。我们还测定了ABCA7基因中一个家族性AD变体和一个临床报道的保护性变体的活性。我们的发现不仅从结构上揭示了 ABCA7 介导的 PS 转运,而且还首次提供了生化证据,证明它通过将脂质转运到载脂蛋白E而与 AD 联系在一起。
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Structural insights into human ABCA7-mediated lipid transport
The human ATP-binding cassette (ABC) transporter ABCA7 participates in the lipidation of apolipoprotein ApoE, a commonly recognized risk factor for Alzheimer’s disease (AD). How ABCA7 is involved in the molecular pathogenesis of AD remains poorly understood. Using cryoelectron microscopy (cryo-EM), we determined ABCA7 structures in the apo and substrate-bound forms, respectively. Combined with activity assays, we assigned the residues that specifically bind two molecules of phosphatidylserine (PS) that are arranged in a “tail-to-tail” manner. Pull-down assays confirmed that ApoE directly interacts with ABCA7; and moreover, both ATPase and lipid transport activities of ABCA7 were significantly enhanced in the presence of ApoE. We also measured the activities of a familial AD variant and a protective clinically reported variant in the ABCA7 gene. Our findings not only give structural insights into ABCA7-mediated PS translocation, but we also provide first biochemical evidence for its link to AD by forwarding lipids to ApoE.
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来源期刊
Structure
Structure 生物-生化与分子生物学
CiteScore
8.90
自引率
1.80%
发文量
155
审稿时长
3-8 weeks
期刊介绍: Structure aims to publish papers of exceptional interest in the field of structural biology. The journal strives to be essential reading for structural biologists, as well as biologists and biochemists that are interested in macromolecular structure and function. Structure strongly encourages the submission of manuscripts that present structural and molecular insights into biological function and mechanism. Other reports that address fundamental questions in structural biology, such as structure-based examinations of protein evolution, folding, and/or design, will also be considered. We will consider the application of any method, experimental or computational, at high or low resolution, to conduct structural investigations, as long as the method is appropriate for the biological, functional, and mechanistic question(s) being addressed. Likewise, reports describing single-molecule analysis of biological mechanisms are welcome. In general, the editors encourage submission of experimental structural studies that are enriched by an analysis of structure-activity relationships and will not consider studies that solely report structural information unless the structure or analysis is of exceptional and broad interest. Studies reporting only homology models, de novo models, or molecular dynamics simulations are also discouraged unless the models are informed by or validated by novel experimental data; rationalization of a large body of existing experimental evidence and making testable predictions based on a model or simulation is often not considered sufficient.
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