反平行(数学)
星形胶质细胞
载脂蛋白B
重组DNA
脂蛋白
化学
载脂蛋白E
生物化学
细胞生物学
神经科学
生物物理学
生物
内科学
胆固醇
医学
基因
中枢神经系统
物理
疾病
量子力学
磁场
作者
Michael R. Strickland,Michael Rau,Brock Summers,Katherine Basore,J. Wulf,Hong Jiang,Yun Chen,Jason D. Ulrich,Gwendalyn J. Randolph,Rui Zhang,James A. J. Fitzpatrick,Anil G. Cashikar,David M. Holtzman
出处
期刊:Neuron
[Elsevier]
日期:2024-01-23
卷期号:112 (7): 1100-1109.e5
被引量:3
标识
DOI:10.1016/j.neuron.2023.12.018
摘要
The Apolipoprotein E gene (APOE) is of great interest due to its role as a risk factor for late-onset Alzheimer's disease. ApoE is secreted by astrocytes in the central nervous system in high-density lipoprotein (HDL)-like lipoproteins. Structural models of lipidated ApoE of high resolution could aid in a mechanistic understanding of how ApoE functions in health and disease. Using monoclonal Fab and F(ab′)2 fragments, we characterize the structure of lipidated ApoE on astrocyte-secreted lipoproteins. Our results provide support for the "double-belt" model of ApoE in nascent discoidal HDL-like lipoproteins, where two ApoE proteins wrap around the nanodisc in an antiparallel conformation. We further show that lipidated, recombinant ApoE accurately models astrocyte-secreted ApoE lipoproteins. Cryogenic electron microscopy of recombinant lipidated ApoE further supports ApoE adopting antiparallel dimers in nascent discoidal lipoproteins.
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