BIOCHEM | Glycolipids

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18 Terms

1

Glycolipid

made out of a lipid and a carbohydrate, it has a structure of one or two fatty acids combined with a mono/oligosaccharide group connected to a sphingolipid or glycerol group backbone

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2

Fatty Acid Chains (in glycolipids)

attached to the backbone

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3

Carbohydrate group (in glycolipids)

gives its hydrophilic property; extends out from the cell membrane to the extracellular space

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4

Properties of Glycolipids

amphipatic, forms bilayer, the hydrophilic carbohydrate portion faces the extracellular environment, non-saponifiable

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5

Functions of Glycolipids

  • make up 3% of the outer layer of the cell membrane

  • membrane stability

  • formation of glycocalyx

  • regulate cell growth

  • determine blood type

  • receptor on surface of red blood cells

  • identify and eliminate pathogen

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6

Glycosphingolipids

Sphingolipid with at least one sugar molecule attached to the ceramide

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7

Cerebrosides

has a single sugar molecule; found in the brain and peripheral nervous tissue, serve as insulators and a protective coating

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8

Gangliosides

neutral compounds with sialic acid residues, has an oligosaccharide, major component of animal cell membrane, especially in the neurons

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9

Glyceroglycolipids

made out of glycerol, fatty acids, carbohydrates and seen in chloroplasts, eukaryotic algae, and cyanobacteria

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10

Glycosylphosphatidylinositols

composed of carbohydrates, lipids, and phosphates lipid anchors in the cell membrane of eukaryotic cells and remodel the cell wall polymers in fungi

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11

Tay-Sachs Disease | Cause and Effect

Caused by deficiency in the enzyme hexosaminidase A and leads to build up of GM2 gangliosides in nerve cells

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12

Tay-Sachs Disease | Symptoms

Progressive neurodegeneration, including muscle weakness, loss of motor skills, and eventually severe cognitive impairment and paralysis

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13

Gaucher Disease | Cause and Effect

Caused by mutations in the GBA gene, leading to deficiency of the enzyme glucocerebrosidase and accumulation of it in various organs

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14

Gaucher Disease | Symptoms

Enlargement of the liver and spleen (hepatosplenomegaly), bone pain and fractures, anemia, and fatigue.

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15

Fabry Disease | Cause and Effect

Caused by deficiency in the enzyme alpha-galactosidase A and buildup of globotriaosylceramide in blood vessels and tissues

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16

Fabry Disease | Symptoms

Pain, particularly in the hands and feet, skin rashes, kidney dysfunction, heart problems, and increased risk of stroke.

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17

Krabbe Disease | Cause and Effect

Caused by deficiency in the enyzme galactocerebrosidase leading to the accumulation of galactosylceramide that destroys myelin, the protective covering of nerve cells

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18

Krabbe Disease | Symptoms

Severe neurological symptoms, including developmental delays, muscle stiffness, irritability, feeding difficulties, progressive loss of motor skills and cognitive functions, often leading to early death

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