The Full Wiki

Glycosaminoglycans: Wikis

Advertisements
  

Note: Many of our articles have direct quotes from sources you can cite, within the Wikipedia article! This article doesn't yet, but we're working on it! See more info or our list of citable articles.

Encyclopedia

(Redirected to Glycosaminoglycan article)

From Wikipedia, the free encyclopedia

Chondroitin sulfate
Hyaluronan (-4GlcUAβ1-3GlcNAcβ1-)n

Glycosaminoglycans[1] (GAGs) or mucopolysaccharides[2] are long unbranched polysaccharides consisting of a repeating disaccharide unit. The repeating unit consists of a hexose (six-carbon sugar) or a hexuronic acid, linked to a hexosamine (six-carbon sugar containing nitrogen).

Contents

Production

Protein cores made in the rough endoplasmic reticulum are posttranslationally modified by glycosyltransferases in the Golgi apparatus, where GAG disaccharides are added to protein cores to yield proteoglycans; the exception is the GAG hyaluronan, which is uniquely synthesized without a protein core and is "spun out" by enzymes at the cell surface directly into the extracellular space.

Function

This family of carbohydrates is essential or important for life.

GAGs form an important component of connective tissues. GAG chains may be covalently linked to a protein to form proteoglycans. Water sticks to GAGs, this is where the resistance to pressure comes from. The density of sugar molecules and the net negative charges attract cations. Ex: Na+, and after the sodium binds it attracts water molecules. Water does not compress, unlike gas.

Some examples of glycosaminoglycan uses in nature include heparin as an anticoagulant, hyaluronan as a component in the synovial fluid lubricant in body joints, and chondroitins which can be found in connective tissues, cartilage and tendons.

Classification

Members of the glycosaminoglycan family vary in the type of hexosamine, hexose or hexuronic acid unit they contain (e.g. glucuronic acid, iduronic acid, galactose, galactosamine, glucosamine).

They also vary in the geometry of the glycosidic linkage.

Examples of GAGs include:

Name Hexuronic acid / Hexose Hexosamine Linkage geometry between predominant monomeric units Unique features
Chondroitin sulfate GlcUA or GlcUA(2S) GalNAc or GalNAc(4S) or GalNAc(6S) or GalNAc(4S,6S) -4GlcUAβ1-3GalNAc β1- Most prevalent GAG
Dermatan sulfate GlcUA or IdoUA or IdoUA(2S) GalNAc or GalNAc(4S) or GalNAc(6S) or GalNAc(4S,6S) -4IdoUAβ1-3GalNAc β1- Distinguished from chondroitin sulfate by the presence of iduronic acid, although some hexuronic acid monosaccharides may be glucuronic acid.[3]
Keratan sulfate Gal or Gal(6S) GlcNAc or GlcNAc(6S) -3Gal(6S)β1-4GlcNAc(6S) β1- Keratan sulfate type II may be fucosylated.[4]
Heparin GlcUA or IdoUA(2S) GlcNAc or GlcNS or GlcNAc(6S) or GlcNS(6S) -4IdoUA(2S)α1-4GlcNS(6S) α1- Highest negative charge density of any known biological molecule
Heparan sulfate GlcUA or IdoUA or IdoUA(2S) GlcNAc or GlcNS or GlcNAc(6S) or GlcNS(6S) -4GlcUAβ1-4GlcNAc α1- Highly similar in structure to heparin, however heparan sulfates disaccharide units are organised into distinct sulfated and non-sulfated domains.[5]
Hyaluronan GlcUA GlcNAc -4GlcUAβ1-3GlcNAc β1- The only GAG that is exclusively non-sulfated
Advertisements

Abbreviations

  • GlcUA = β-D-glucuronic acid
  • GlcUA(2S) = 2-O-sulfo-β-D-glucuronic acid
  • IdoUA = α-L-iduronic acid
  • IdoUA(2S) = 2-O-sulfo-α-L-iduronic acid
  • Gal = β-D-galactose
  • Gal(6S) = 6-O-sulfo-β-D-galactose
  • GalNAc = β-D-N-acetylgalactosamine
  • GalNAc(4S) = β-D-N-acetylgalactosamine-4-O-sulfate
  • GalNAc(6S) = β-D-N-acetylgalactosamine-6-O-sulfate
  • GalNAc(4S,6S) = β-D-N-acetylgalactosamine-4-O, 6-O-sulfate
  • GlcNAc = α-D-N-acetylglucosamine
  • GlcNS = α-D-N-sulfoglucosamine
  • GlcNS(6S) = α-D-N-sulfoglucosamine-6-O-sulfate

References

  1. ^ glycosaminoglycan at Dorland's Medical Dictionary
  2. ^ mucopolysaccharide at Dorland's Medical Dictionary
  3. ^ Trowbridge JM, Gallo RL. (2002). "Dermatan sulfate: new functions from an old glycosaminoglycan". Glycobiology 12 (9): 117R–125R. doi:10.1093/glycob/cwf066. PMID 12213784.  
  4. ^ Funderburgh JL. (2000). "Keratan sulfate: structure, biosynthesis, and function". Glycobiology 10 (10): 951–958. doi:10.1093/glycob/10.10.951. PMID 11030741.  
  5. ^ Gallagher, J.T., Lyon, M. (2000). "Molecular structure of Heparan Sulfate and interactions with growth factors and morphogens". in Iozzo, M, V.. Proteoglycans: structure, biology and molecular interactions. Marcel Dekker Inc. New York, New York. pp. 27–59.  

See also

External links


Advertisements






Got something to say? Make a comment.
Your name
Your email address
Message