Lipid nanodisc scaffold and size alter the structure of a pentameric ligand-gated ion channel

被引:16
|
作者
Dalal, Vikram [1 ]
Arcario, Mark J. [1 ]
Petroff II, John T. [1 ]
Tan, Brandon K. [1 ]
Dietzen, Noah M. [1 ]
Rau, Michael J. [2 ]
Fitzpatrick, James A. J. [2 ]
Brannigan, Grace [3 ,4 ]
Cheng, Wayland W. L. [1 ]
机构
[1] Washington Univ, Sch Med, Dept Anesthesiol, St Louis, MO 63110 USA
[2] Washington Univ, Ctr Cellular Imaging, Sch Med, St Louis, MO USA
[3] Rutgers State Univ, Ctr Computat & Integrat Biol, Camden, NJ USA
[4] Rutgers State Univ, Dept Phys, Camden, NJ USA
关键词
FORCE-FIELD; MECHANISM; AUTOMATION; SIMULATION; GUI;
D O I
10.1038/s41467-023-44366-w
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Lipid nanodiscs have become a standard tool for studying membrane proteins, including using single particle cryo-electron microscopy (cryo-EM). We find that reconstituting the pentameric ligand-gated ion channel (pLGIC), Erwinia ligand-gated ion channel (ELIC), in different nanodiscs produces distinct structures by cryo-EM. The effect of the nanodisc on ELIC structure extends to the extracellular domain and agonist binding site. Additionally, molecular dynamic simulations indicate that nanodiscs of different size impact ELIC structure and that the nanodisc scaffold directly interacts with ELIC. These findings suggest that the nanodisc plays a crucial role in determining the structure of pLGICs, and that reconstitution of ion channels in larger nanodiscs may better approximate a lipid membrane environment. The authors show that lipid nanodiscs of different scaffold type and size alter the structure of the pentameric ligand-gated ion channel, ELIC. The results suggest that nanodisc selection is an important consideration for structural studies of membrane proteins.
引用
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页数:10
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