Comparative proteomic analysis of membrane microdomains isolated from two hyperlipidemic animal models

Biochim Biophys Acta. 2016 Sep;1864(9):1061-1071. doi: 10.1016/j.bbapap.2016.05.009. Epub 2016 May 26.
No abstract available

Keywords: Atherosclerosis; Hyperlipidemia; Mass spectrometry; Membrane microdomains; Nano-chromatography; Proteomics.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigen Presentation / drug effects
  • Apolipoproteins E / deficiency
  • Apolipoproteins E / genetics
  • Cell Movement / drug effects
  • Citric Acid Cycle / drug effects
  • Diet, High-Fat
  • Disease Models, Animal
  • Focal Adhesions / drug effects
  • Gene Ontology
  • Humans
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors / pharmacology*
  • Hyperlipidemias / drug therapy
  • Hyperlipidemias / etiology
  • Hyperlipidemias / genetics
  • Hyperlipidemias / metabolism*
  • Hypolipidemic Agents / pharmacology*
  • Leukocytes / cytology
  • Leukocytes / drug effects
  • Male
  • Membrane Microdomains / chemistry
  • Membrane Microdomains / drug effects*
  • Membrane Proteins / genetics
  • Membrane Proteins / isolation & purification*
  • Membrane Proteins / metabolism
  • Mesocricetus
  • Mice, Knockout
  • Molecular Sequence Annotation
  • Phagosomes / drug effects
  • Phagosomes / metabolism
  • Proteomics / methods*
  • Receptors, Cell Surface / genetics
  • Receptors, Cell Surface / metabolism
  • Signal Transduction
  • Tight Junctions / drug effects

Substances

  • Apolipoproteins E
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors
  • Hypolipidemic Agents
  • Membrane Proteins
  • Receptors, Cell Surface
  • extracellular matrix receptor