In situ delipidation-based structure of low-density lipoprotein and apolipoprotein B-100 physiologically imaged by atomic force microscopy

Int J Biol Macromol. 2026 Mar:351:151070. doi: 10.1016/j.ijbiomac.2026.151070. Epub 2026 Feb 23.

Abstract

Apolipoprotein B-100 (apoB-100) is the main structural protein of apoB-containing lipoproteins including low-density lipoprotein (LDL). Its organization or lipidation process in an apoB-containing lipoprotein particle is still unclear. To understand its organization in a LDL particle, the combination of atomic force microscopy (AFM) with lipid depletion by Nonidet P-40 (NP-40) or methyl-β-cyclodextrin (MβCD) was utilized for the first time to in situ visualize LDL delipidation process and lipid-poor/-free apoB-100 at a physiological condition. During LDL delipidation process, different morphologies/structures were visualized successively including spheroidal structure with a smaller size than native LDL, spheroidal structure with one or more holes, closed annular/circular structure, opened annular/circular structure, C/U-shaped (or horseshoe-shaped) structure, and V/S/I-shaped structure. Based on the concentration-dependent structural distributions, these structures probably reflect 5 stages of LDL delipidation (e.g., a slightly delipidated LDL stage, a partially delipidated LDL stage, a neutral lipid-poor/-free apoB-100 stage, a lipid-poor apoB-100 stage, and a lipid-free apoB-100 stage, respectively). Our findings could provide structural evidence to reconcile the previous controversy and provide potential evidence/clues/implications for understanding apoB-100 lipidation and the organization of apoB-100 in apoB-containing lipoprotein particles. Potentially, this study also can provide new structural insights into the design of food-grade lipid carriers. Moreover, the combination of AFM with lipid depletion, which has many advantages over traditional electron microscopy (e.g., label-free, in situ, and real-time imaging under physiological conditions, etc.), is a potentially ideal novel strategy for studying the structure of apolipoproteins or lipoproteins.

Keywords: Apolipoprotein B-100 (apoB-100); Atherosclerosis; Atomic force microscopy (AFM); Food colloids; Lipid carrier; Low-density lipoprotein (LDL); apoB-100 lipidation.

MeSH terms

  • Apolipoprotein B-100* / chemistry
  • Apolipoprotein B-100* / metabolism
  • Humans
  • Lipoproteins, LDL* / chemistry
  • Lipoproteins, LDL* / metabolism
  • Lipoproteins, LDL* / ultrastructure
  • Microscopy, Atomic Force*

Substances

  • Apolipoprotein B-100
  • Lipoproteins, LDL