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Lysosomal degradation of membrane lipids
- Source :
- FEBS Letters. 584:1700-1712
- Publication Year :
- 2009
- Publisher :
- Wiley, 2009.
-
Abstract
- The constitutive degradation of membrane components takes place in the acidic compartments of a cell, the endosomes and lysosomes. Sites of lipid degradation are intralysosomal membranes that are formed in endosomes, where the lipid composition is adjusted for degradation. Cholesterol is sorted out of the inner membranes, their content in bis(monoacylglycero)phosphate increases, and, most likely, sphingomyelin is degraded to ceramide. Together with endosomal and lysosomal lipid-binding proteins, the Niemann–Pick disease, type C2-protein, the GM2-activator, and the saposins sap-A, -B, -C, and -D, a suitable membrane lipid composition is required for degradation of complex lipids by hydrolytic enzymes.
- Subjects :
- Ceramide
Endosome
Membrane lipids
Vesicular Transport Proteins
Biophysics
Biology
Models, Biological
Biochemistry
Saposins
Membrane Lipids
03 medical and health sciences
chemistry.chemical_compound
0302 clinical medicine
Sphingolipid activator protein
Structural Biology
Lysosome
Genetics
medicine
Animals
Humans
Phosphatidylinositol
Molecular Biology
Glycoproteins
030304 developmental biology
Niemann–Pick disease, type C2-protein
Antigen Presentation
0303 health sciences
G(M2) Activator Protein
Biological Transport
Cell Biology
Lipid Metabolism
GM2-activator
Endocytosis
medicine.anatomical_structure
Membrane
chemistry
Saposin
lipids (amino acids, peptides, and proteins)
NPC1
Carrier Proteins
Lysosomes
Sphingomyelin
030217 neurology & neurosurgery
Signal Transduction
Subjects
Details
- ISSN :
- 00145793
- Volume :
- 584
- Database :
- OpenAIRE
- Journal :
- FEBS Letters
- Accession number :
- edsair.doi.dedup.....b499b2ecf8753e54a741b14b590e2494