EMD-9089

Tomography
59.9 Å
EMD-9089 Deposition: 03/09/2018
Map released: 09/01/2019
Last modified: 25/12/2019
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EMD-9089

Single-Molecule 3D Image of Human Plasma Intermediate-Density Lipoprotein in Complex with Monoclonal Antibody MAB012 (No. 05)

EMD-9089

Tomography
59.9 Å
EMD-9089 Deposition: 03/09/2018
Map released: 09/01/2019
Last modified: 25/12/2019
Overview Sample Experiment Validation Volume Browser Additional data Links
Sample Organism: Homo sapiens, Mus musculus
Sample: Human plasma intermediate-density lipoprotein in complex with monoclonal antibody mAB012

Deposition Authors: Lei D, Yu Y, Kuang Y, Krauss R, Ren G
Single-molecule 3D imaging of human plasma intermediate-density lipoproteins reveals a polyhedral structure.
Lei D, Yu Y, Kuang YL, Liu J , Krauss RM, Ren G
(2018) Biochim Biophys Acta Mol Cell Biol Lipids , 1864 , 260 - 270
PUBMED: 30557627
DOI: doi:10.1016/j.bbalip.2018.12.004
ISSN: 1879-2618
Abstract:
Intermediate-density lipoproteins (IDLs), the remnants of very-low-density lipoproteins via lipolysis, are rich in cholesteryl ester and are associated with cardiovascular disease. Despite pharmacological interest in IDLs, their three-dimensional (3D) structure is still undetermined due to their variation in size, composition, and dynamic structure. To explore the 3D structure of IDLs, we reconstructed 3D density maps from individual IDL particles using cryo-electron microscopy (cryo-EM) and individual-particle electron tomography (IPET, without averaging from different molecules). 3D reconstructions of IDLs revealed an unexpected polyhedral structure that deviates from the generally assumed spherical shape model (Frias et al., 2007; Olson, 1998; Shen et al., 1977). The polyhedral-shaped IDL contains a high-density shell formed by flat surfaces that are similar to those of very-low-density lipoproteins but have sharper dihedral angles between nearby surfaces. These flat surfaces would be less hydrophobic than the curved surface of mature spherical high-density lipoprotein (HDL), leading to a lower binding affinity of IDL to hydrophobic proteins (such as cholesteryl ester transfer protein) than HDL. This is the first visualization of the IDL 3D structure, which could provide fundamental clues for delineating the role of IDL in lipid metabolism and cardiovascular disease.