TG, PL, SPL Flashcards
TG and PL are synthesized _
cytosolic side of ER and lesser extent OMM
Common intermediate of TG and PL synthesis
Phosphatidic Acid
Major stored form of E in adipose
TG
Formation of TG
Glyercol 3P > PA > diacyl glycerol > TG
CM transports TG to _ and dietary cholesterol to _
Various tissues(muscle adipocytes)
Liver only
Apoproteins on CM
- ApoC…activates lipoprotein lipase > hydrolyze TG > release F.A. for storage/E in adipocytes or muscle
- ApoB48…marker of CM
- ApoE…recognition protein
- ApoB48, ApoE responsible for cholesterol transport to liver by remnant CM via endocytosis
LDL has which apoprotein?
Deficiency can cause?
- Apo100
- Hypercholesterolemia
Formation of PL(de novo)
PA > CDP-DAG by cytidyl transferase…+ serine > PS and CMP
or CDP-DAG + inositol > PI(CNS)
Dipalmitoyl PC deficiency in lung
Respiratory distress syndrome
_ cause skin cancer by activating PKC
They are structural analogues of _
- Phorbol esters
- DAG
PL salvage pathway
Methionine intake limited > choline re-salvaged > choline phosphate > CDP-choline via cytidyl transferase…+ DAG > PC
Defect in salvage pathway leads to(kinase or transferase)
Fatty liver
(DAG accumulates > TG)
PL drug carrier _
Liposome
Hydrolyze…
PLA1:
PLA2:
PLC:
PLD:
- first ester bond
- fatty acyl ester bond at position 2
- releases head groups of PL + DAG
- releases head groups + PA
T/F: Sphingolipids are involved in ABO blood types
True
Synthesis of SPL occurs in _
ER membrane
RDS in SPL synthesis
Serine palmitoyl transferase(B6)
Palmitic acid + serine
SPL synthesis steps
after RDS rxn…keto > sphinganine > dihydroceramide > ceramide via cermide synthase
PAPS?
- Phosphoadenosyl phosphosulfate
- Sulfates neutral glycolipids > sulfatids
SPL catabolism(lysosomal enzymes)
Release CBHY > Ceramide > sphingosine + F.A. via ceramidase(amide)
Sphingolipidoses characterized by (4)
- abnormal amount of SPL > organomegaly
- Defect in catabolic enzymes only
- Affect all tissues the same
- Mental retardation
Gaucher’s:
Krabbe’s:
Nielmann-pick:
Tay Sacch’s:
Farber’s:
- Glucocerebrosidase deficiency
- Galactocerebrosidase deficiency
- Sphingomyelinase deficiency
- Hexoaminidase deficiency
- Ceramidase deficiency
Opposed to sphingolipidoses, demyelination/degradation causes _
Multiple sclerosis