Complex Lipids II Flashcards

1
Q

What are the 3 classes of glycerolipids?

A
  • Triacylglycerols (TAGs) - 3 FA
  • Glycerophospholipids - 2FA and Headgroup
  • Ether Glycerolipids - 1 FA, 1 Ether, Headgroup
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2
Q

What is the major store of lipids in the body?

A

TAG

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3
Q

What glycerolipids are involved in signal transduction?

A
  • DAG (diacylglycerol)

- Arachondonic acid

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4
Q

Sphingomyelin, phosphatidylcholine, and glycerolipids can be found where in the cell?

A

Often found in the outer leaflet of the membrane, associated with cell-cell recognition

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5
Q

Phosphatidylserine, Phosphatidylethanolamine, Phosphatidylinositol can call be found where?

A

Often found in the inner leaflet of the membrane

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6
Q

Cleavage of Phosphatidylinositol by phospholipase A1 would result in what products?

A
  • Saturated Fatty acid

- glycerol backbone with unsaturated fatty acid with a 1-phosphoinositol head group left

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7
Q

What is the position of the ether in ether glycerolipids?

A

1 position on the glycerol

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8
Q

What are two types of ether glycerolipids?

A
  • Plasmalogen

- PAF (Platelet activating factor)

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9
Q

Where can Plasmogens be found?

A
  • Mitochondrial Lipids
  • Myelin
  • Muscle
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10
Q

What is PAF?

- What does it do?

A
  • Platelet Activating Factor, released from phagocytic blood cells in response to stimuli

Causes:

  • Platelet aggregation
  • Edema
  • Hypotension
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11
Q

What do you need to synthesize PAF?

A
  • NADPH, AcylCoA, DHAP, activated ethanolamine

* these things take energy to make

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12
Q

What are the 3 major sphingolipid components of the plasma membrane?

A
  • Sphingophospholipids

- Glycolipids

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13
Q

What types of problems arise when sphingolipids can’t be broken down?
- Where is this defect usually found?

A
  • Neural defects often arise because these are prominent in neural tissue
  • Lysosome - usually the location of degradation issues
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14
Q

T or F: both types of sphingolipids have fatty acids linked to them.

A

True - this fatty acids amide linkage to sphingosine is called ceramide

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15
Q

T or F: sphingolipids are involved in cell-cell, cell-matrix interactions.

A

True

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16
Q

T or F: Spingolipids responsible for the A, B, and O blood types.

17
Q

What does a glycolipid consist of?

A
  • Ceramide connected to a sugar
18
Q

T or F: The glycolipids contain phosophdiester linkages between the sphigosine backbone and ceramide.

A

False, glycolipids simply have a sugar connected to ceramide

19
Q

What if the variable factor between different glycolipids?

A

Carbohydrate head groups only

20
Q

What is attached to a ceramide group to make sphingomyelin?

A

Phosphocholine

21
Q

What is mucolipidosis?

A
  • Inability to degrade glycolipids and sphigomyelin in membranes
22
Q

What are some examples diseases that cause mucolipidosis?

A
  • Gaucher’s Disease
  • Tay-Sachs Disease
  • Fabray’s Disease
23
Q

Cerebrosides, gangliosides, sulfatides, and globosides are all examples of what?

A

Glycolipids

24
Q

T or F: glycolipids contain phosphate

25
Where are glycolipids most predominant?
Especially predominant in neural cell types
26
What are the two classes of acidic glycolipids? | - what is their charge at physiological pH?
- Sulfatides (sulfate added) - Gangliosides (NANA group added) Negatively charged at physiological pH
27
Where does glycolipid synthesis and breakdown occur?
Synthesis: ER and Golgi Breadown: Lysosome
28
What adds sulfate groups to sugars to make sulfatides?
PAPS
29
How are sugars added to ceramide to make glycolipids?
- Sugar is activated with UDP or CMP then added
30
What kind(s) of bond(s) link(s) fatty acids in sphingolipids and glycolipids?
Amide (NOT ester or ether)
31
What is needed to synthesize ceramide?
``` Serine Palmitoyl-CoA FACoA NADPH FAD ```
32
What kind of environment is needed for lysosomal acid hydrolases to work?
Low pH
33
What happens if sphingolipid degradation is blocked in sphingolipids?
- Synthesis will continue | - You will get an accumulation of degradation products