GAGs and glycoproteins Flashcards

1
Q

Other names for GAGs

A

Glycosaminoglycans, mucopolysaccharides, proteoglycans (I think that has a slightly more specific meaning but it doens’t matter for us so use it interchangably)

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2
Q

Basic properties of GAGs

A

repeating disaccharide units (amino sugar, acid sugar)
gel-like matrix, H2O binding, form ground substance, lubricating, stabilize and support cellular and fibrous components of tissue, maintain H2O and salt balance

stong negative charges, hydrated shell, compressible

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3
Q

Fxns of GAGs

A

cell shape maintenance, adhesion, migration, cell-cell communication, source of growth factors

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4
Q

Sugars in GAGs

A

Amino: D-glucosamine or D-Galactosamine
Acidic: D-glucuronic acid or L-iduronic acid
Keratan sulfate uses galactose

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5
Q

Major GAGs

A

Hyaluron (ic acid), Chondroitin sulfate, Keratan sulfate, Heparin, Heparan sulfate

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6
Q

Hyaluron

A

Hyaluronic acid, HA

No sulfates, not covalently linked to proteins

synovial fluid, vitreous humor, loose CT

large polymers, shock absorbing

D-glucuronic acid, N-Ac-D-glucosamine

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7
Q

Chondroitin sulfate

A

Most abundant GAG

cartilage, bone, heart valves

D-glucuronic acid, N-Acetyl-D-galactosamine (sulfated)

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8
Q

Keratan sulfate

A

aggregated with chondroitin sulfates

cornea, bone, cartilage

D-galactose, N-acetyl-D-glucosamine (sulfated)

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9
Q

Dermatan sulfate

A

Found in skin, blood vessels, heart valves

L-iduronic acid (sulfated), N-Ac-D-galactosamine (sulfated)

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10
Q

Heparin

A

component of intracellular granules in Mast cells lining arteries of lungs, liver and skin

More sulfated than heparan sulfates

D-Glucuronic or L-Iduronic acid (sulfated), N-Acetyl or N-sulfo-DGlucosamine

Anti-coagulent: Induces release of cell surface-associated TFPI (tissue factor pathyway inhibitor, anti-thrombin III)

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11
Q

Heparan sulfate

A

higher acetylated glucosamine than heparin

basement membranes, component of cell surfaces

D-Glucuronic or L-Iduronic acid (sulfated), N-Acetyl or N-sulfo-DGlucosamine

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12
Q

Strucutre of proteoglycans

A

attached to proteins (excpet HA) covallently attaced to protein to form proteoglycan monomers

≥100 monosaccharides

bottle brush

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13
Q

proteoglycan aggregates

A

chondroitin and keratin sulfates (i.e.: in cartilage) attached to protein core bound nonvovalently to HA (link proteins)

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14
Q

Linking sugars of proteoglycans

A

Gal-Gal-Xyl usually bound to Ser (Thr most likely alternative)

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15
Q

Steps of proteoglycan synthesis

A

synthesis of: amino sugars, acidic sugars, core protein, carbohydrate chain; addition of sulfate groups

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16
Q

Addition of sufate groups

A

ATP-sulfurase: ATP + SO42- –>Adenosine 5;-phosphosulfate (APS) + PPi
APS-kinase: APS + ATP –> 3’-phosphoadenoside 5’-phosphosulfate (PAPS) + ADP

Sulfotransferase: PAPS + sugar –> sulfated sugar + adenosine-5’, 3’-bisphosposphate

17
Q

Locations for proteoglycan synthesis

A

protein: cytosol/rER
Linker sugars added: ER (UDP-xyl, then 2x UDP-Gal)
Everything else: Golgi

18
Q

Warfarin

A

Vitamin K analog, anti-coagulent. Inhibits modification of several coagulation factors

slower acting than heparin, usually adminstered after

19
Q

TFPI

A

tissue factor pathway inhibitor, anti-thrombin III

binds factor Xa and VIIa forming inactive quaternary complex

20
Q

Applications of HA

A

used as lubricant to protect corneal endothelium in ocular surgery, god for patients with osteoarthritis (OA), anti-adhesive may be good for postsurgical wound healing

21
Q

Functions of glycoproteins

A

membrane bound: 1. cell surface recognition; 2. cell surface antigenicity; 3. componets of ECM; 4. contribute to glycocalyx and cellular protection

secreted glycoproteins: part of ECM, lubricants

intracellular: lysosomal enzymes

22
Q

Glycoprotein definition

A

protein with short oligosaccharide chain (2-10 residues), may or may not be branched or negatively charged

23
Q

Glycoproteins and cellular infections

A

E. coli –> adhere to mannose residues on plasma membrane of human cheek cells

H. pylori –> interact with blood group antigen on gastric endothelium (ulcers)

24
Q

Blood types

A

O-linked surgars (H substance) to protein (band 3?) or ceramide

25
Mucins
Large, negatively charged, NANA (N-acetyl neuraminic acid), trap H2O, protective barriers
26
N-Linked oligosaccharides
linked to amino group of Asn Complex: N-acetylglucosamine (GlcNAc), L-Fucose (Fuc) and NANA High mannose: mostly just mannose
27
O-linked oligosaccharides
linked to Ser or The (Hyl in collagen) often GalNAc collagen has glucose-galactose dimer
28
Synthesis of Glycoproteins: prep of sugars
Glucoseamine-->uses UDP-glucosamine NANA-->uses CMP-NANA Amine groups come from Gln
29
Synthesis of O-linked glycoproteins
protein synthesized in rER glycosylation in golgi, use specific glycosyltransferases, add sugars sequentially begins with transfer of GlcNAc (from UDP-GlcNAc) to Ser or Thr intracellular are free within golgi, for cell membrane become part of golgi membrane with carb on outside
30
Synthesis of N-linked glycoproteins
1. protein synthesized in rER 2 & 3. ER: oligosaccharide constructed onto dolichol through pyrophosphate linkage (use membrane bound glycosyltransferases, 1)GlcNAc 2)Man 3)glu 4. oligosaccharide transfered by protein-oligosaccharide tranferase in ER (to Asn) 5. processed by removal of specific mannosyl and glucosyl resudues (ER) 6-7. Final processing in golgi: complex-add other sugars; final processing like O-linked
31
Degredation of GAGs and Glycoproteins
Occurs in lysosomes following endocytosis
32
Mucopolysaccaridosis
inability to degrade GAGs or glycoproteins
33
Shingolipidosis
inability to degrade sphingolipids
34
Enzyme transport to lysosomes
lysosomal enzymes tagged with N-linked mannose 6 phosphate inability to tag leads to I-cell disease