Lipids Flashcards

1
Q

What is the common and defining feature of lipids?

A

Insolubility in water

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2
Q

What are the main biological functions of lipids?

A

Energy storage
Structural components of cell membranes
Important signalling molecules

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3
Q

What are the 5 common classes of lipids in eukaryotic cells?

A

Fatty acids
Triacylglycerols
Phospholipids
Glycolipids
Sterols

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4
Q

What are fatty acids?

A

Carboxylic acids with hydrocarbon chains

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5
Q

What affects the physical properties of fatty acids?

A

Degree of unsaturated bonds

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6
Q

Are saturated or unsaturated fatty acids liquid at room temperature?

A

Saturated

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7
Q

What are fatty acdis named by?

A

Length of the hydrocarbon chain and number and position of any carbon-carbon double bonds

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8
Q

What are the essential fatty acids?

A

Polyunsaturated fatty acids that cannot be synthesised by humans and must be obtained from the diet e.g. omega-3 fatty acids and omega-6 fatty acids

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9
Q

What are triaclyglycerols?

A

Composed of three fatty acids covalently joined to glycerol through ester linkages

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10
Q

What do triacylglycerols do?

A

Provide stored energy and are stockpiled in adipocytes in humans

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11
Q

What is the main role of phospholipids and glycolipids?

A

Structure

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12
Q

What is the basic structure of phospholipids and glycolipids?

A

A backbone
At least one fatty acid
Something else

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13
Q

What are the two backbones possible for phospholipids and glycolipids?

A

Glycerol
Sphingosine

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14
Q

What are sphingolipids?

A

Phospholipids or glycolipids with a sphingosine backbone

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15
Q

What are sterols?

A

Precursors to other biomolecules such as steroid hormones and bile acids

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16
Q

What are sterols synthesised from?

A

Simple five carbon structures called isoprenes

17
Q

What is the family of cholesterol inhibitors and give an example of one?

A

Statins
Rosuvastatin

18
Q

What are the roles of cholesterol?

A

Production of sex hormones
Assists in bile production in liver
Building block for human tissues
Creating Vitamin D

19
Q

What is Niemann-Pick Disease?

A

Lysosomal storage disease characterised by a sphingomyelin metabolism disorder

20
Q

What causes Niemann-Pick Disease?

A

Rare autosomal recessive genetic defect in the gene encoding the enzyme sphingomyelinase resulting in a build up of sphingomyelin in the brain, spleen , liver and lungs

21
Q

What is the outcome for those with Niemann-Pick Disease?

A

Develops in infancy and leads to mental impairment and eventually death

22
Q

What is Tay-Sachs Disease?

A

Lysosomal storage disease due to mutations in the HEXA gene causing a build up of gangliosides in brain

23
Q

What does the HEXA gene do?

A

Encodes the hexosaminidase A enzymes which catalyses the degradation of gangliosides

24
Q

What is the outcome of a patient with Tay-Sachs Disease?

A

Progressive deterioration of nerve cells and of mental/physical capabilities that begins at ~6 months and usually results in death by age 4

25
Q

What causes Batten disease?

A

Build up of lipofuscins (deposits of fats and proteins) in tissues
CLN3 gene defect is the most common cause of this disease

26
Q

What are the usual symptoms of Batten Disease?

A

Visual problems and seizures and develop between the ages of 2 and 10

27
Q

What does the CLN3 gene do?

A

Encode for battenin which localises to lysosomes and endosomes but its function is unknown