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词条 Glycolipid
释义

  1. Structure

  2. Metabolism

     Glycosyltransferases  Glycoside hydrolases  Defects in metabolism 

  3. Function

     Cell–cell interactions  Immune responses  Blood types 

  4. Types of glycolipids

  5. See also

  6. References

  7. External links

{{Use dmy dates|date=June 2016}}{{distinguish|Lipopolysaccharide}}Glycolipids are lipids with a carbohydrate attached by a glycosidic (covalent) bond.[1] Their role is to maintain the stability of the cell membrane and to facilitate cellular recognition, which is crucial to the immune response and in the connections that allow cells to connect to one another to form tissues.[2] Glycolipids are found on the surface of all eukaryotic cell membranes, where they extend from the phospholipid bilayer into the extracellular environment.[2]

Structure

The essential feature of a glycolipid is the presence of a monosaccharide or oligosaccharide bound to a lipid moiety. The most common lipids in cellular membranes are glycerolipids and sphingolipids, which have glycerol or a sphingosine backbones, respectively. Fatty acids are connected to this backbone, so that the lipid as a whole has a polar head and a non-polar tail. The lipid bilayer of the cell membrane consists of two layers of lipids, with the inner and outer surfaces of the membrane made up of the polar head groups, and the inner part of the membrane made up of the non-polar fatty acid tails.

The saccharides that are attached to the polar head groups on the outside of the cell are the ligand components of glycolipids, and are likewise polar, allowing them to be soluble in the aqueous environment surrounding the cell.[3] The lipid and the saccharide form a glycoconjugate through a glycosidic bond, which is a covalent bond. The anomeric carbon of the sugar binds to a free hydroxyl group on the lipid backbone. The structure of these saccharides varies depending on the structure of the molecules to which they bind.

Metabolism

Glycosyltransferases

Enzymes called glycosyltransferases link the saccharide to the lipid molecule, and also play a role in assembling the correct oligosaccharide so that the right receptor can be activated on the cell which responds to the presence of the glycolipid on the surface of the cell. The glycolipid is assembled in the Golgi apparatus and embedded in the surface of a vesicle which is then transported to the cell membrane. The vesicle merges with the cell membrane so that the glycolipid can be presented on the cell's outside surface.[4]

Glycoside hydrolases

Glycoside hydrolases catalyze the breakage of glycosidic bonds. They are used to modify the oligosaccharide structure of the glycan after it has been added onto the lipid. They can also remove glycans from glycolipids to turn them back into unmodified lipids.[5]

Defects in metabolism

Sphingolipidoses are a group of diseases that are associated with the accumulation of sphingolipids which have not been degraded correctly, normally due to a defect in a glycoside hydrolase enzyme. Sphingolipidoses are typically inherited, and their effects depend on which enzyme is affected, and the degree of impairment. One notable example is Niemann–Pick disease which can cause pain and damage to neural networks, and is usually fatal in early infancy.[6]

Function

Cell–cell interactions

The main function of glycolipids in the body is to serve as recognition sites for cell–cell interactions. The saccharide of the glycolipid will bind to a specific complementary carbohydrate or to a lectin (carbohydrate-binding protein), of a neighboring cell. The interaction of these cell surface markers is the basis of cell recognitions, and initiates cellular responses that contribute to activities such as regulation, growth, and apoptosis.[7]

Immune responses

An example of how glycolipids function within the body is the interaction between leukocytes and endothelial cells during inflammation. Selectins, a class of lectins found on the surface of leukocytes and endothelial cells bind to the carbohydrates attached to glycolipids to initiate the immune response. This binding causes leukocytes to leave circulation and congregate near the site of inflammation. This is the initial binding mechanism, which is followed by the expression of integrins which form stronger bonds and allow leukocytes to migrate toward the site of inflammation.[8] Glycolipids are also responsible for other responses, notably the recognition of host cells by viruses.[9]

Blood types

Blood types are an example of how glycolipids on cell membranes mediate cell interactions with the surrounding environment. The four main human blood types (A, B, AB, O) are determined by the oligosaccharide attached to a specific glycolipid on the surface of red blood cells, which acts as an antigen. The unmodified antigen, called the H antigen, is the characteristic of type O, and is present on red blood cells of all blood types. Blood type A has an N-acetylgalactosamine added as the main determining structure, type B has a galactose, and type AB has all three of these antigens. Antigens which are not present in an individual's blood will cause antibodies to be produced, which will bind to the foreign glycolipids. For this reason, people with blood type AB can receive transfusions from all blood types (the universal acceptor), and people with blood type O can act as donors to all blood types (the universal donor).[10]

Types of glycolipids

{{Expand list|date=August 2008}}
  • Glyceroglycolipids: a sub-group of glycolipids characterized by an acetylated or non-acetylated glycerol with at least one fatty acid as the lipid complex. Glyceroglycolipids are often associated with photosynthetic membranes and their functions. The subcategories of glyceroglycolipids depend on the carbohydrate attached.[11]
    • Galactolipids: defined by a galactose sugar attached to a glycerol lipid molecule. They are found in chloroplast membranes and are associated with photosynthetic properties.[11]
    • Sulfolipids: have a sulfur-containing functional group in the sugar moiety attached to a lipid. An important group is the sulfoquinovosyl diacylglycerols which are associated with the sulfur cycle in plants.[12]
  • Glycosphingolipids: a sub-group of glycolipids based on sphingolipids. Glycosphingolipids are mostly located in nervous tissue and are responsible for cell signaling.[13]
    • Cerebrosides: a group glycosphingolipids involved in nerve cell membranes.[14]
    • Galactocerebrosides: a type of cerebroseide with galactose as the saccharide moiety
    • Glucocerebrosides: a type of cerebroside with glucose as the saccharide moiety; often found in non-neural tissue.
    • Sulfatides: a class of glycolipids containing a sulfate group in the carbohydrate with a ceramide lipid backbone. They are involved in numerous biological functions ranging from immune response to nervous system signaling.
    • Gangliosides: the most complex animal glycolipids. They contain negatively charged oligosacchrides with one or more sialic acid residues; more than 200[15] different gangliosides have been identified. They are most abundant in nerve cells.
    • Globosides: glycosphingolipids with more than one sugar as part of the carbohydrate complex. They have a variety of functions; failure to degrade these molecules leads to Fabry disease.
    • Glycophosphosphingolipids: complex glycophospholipids from fungi, yeasts, and plants, where they were originally called "phytoglycolipids". They may be as complicated a set of compounds as the negatively charged gangliosides in animals.
    • Glycophosphatidylinositols: a sub-group of glycolipids defined by a phosphatidylinositol lipid moiety bound to a carbohydrate complex. They can be bound to the C-terminus of a protein and have various functions associated with the different proteins they can be bound to.[16]

See also

  • Sophorolipids
  • Rhamnolipid
  • Glycocalyx
  • Glycome
  • Glycoproteins
  • Niemann Pick disease

References

1. ^{{cite book|last1=Voet|first1=Donald|last2=Voet|first2=Judith|last3=Pratt|first3=Charlotte | name-list-format = vanc |title=Fundamentals of Biochemistry Life at the Molecular Level|date=2013|publisher=John Wiley & Sons, Inc.|location=Hoboken, NJ|isbn=9781118129180|edition=Fourth }}
2. ^1 {{cite web|title=Glycolipids|url=http://www.nature.com/subjects/glycolipids#research-and-reviews|website=nature|publisher=Nature Publishing Group|access-date=2015-11-01}}
3. ^{{cite journal | vauthors = Aureli M, Grassi S, Prioni S, Sonnino S, Prinetti A | title = Lipid membrane domains in the brain | journal = Biochimica et Biophysica Acta | volume = 1851 | issue = 8 | pages = 1006–16 | date = August 2015 | pmid = 25677824 | doi = 10.1016/j.bbalip.2015.02.001 }}
4. ^{{cite journal | vauthors = Williams GJ, Thorson JS | title = Natural product glycosyltransferases: properties and applications | journal = Advances in Enzymology and Related Areas of Molecular Biology | volume = 76 | pages = 55–119 | date = 2009 | pmid = 18990828 | doi = 10.1002/9780470392881.ch2 | series = Advances in Enzymology - and Related Areas of Molecular Biology | isbn = 9780470392881 }}
5. ^{{cite journal | vauthors = Sinnott ML |title=Catalytic mechanism of enzymic glycosyl transfer |journal=Chemical Reviews |date=November 1990 |volume=90 |issue=7 |pages=1171–1202 |doi=10.1021/cr00105a006}}
6. ^{{cite journal | vauthors = Sandhoff K | title = Sphingolipidoses | journal = Journal of Clinical Pathology | volume = 8 | issue = 12 | pages = 94–105 | date = 1974 | pmid = 4157247 | pmc = 1347206 | doi = 10.1136/jcp.s3-8.1.94 }}
7. ^{{cite journal | vauthors = Schnaar RL | title = Glycolipid-mediated cell-cell recognition in inflammation and nerve regeneration | journal = Archives of Biochemistry and Biophysics | volume = 426 | issue = 2 | pages = 163–72 | date = June 2004 | pmid = 15158667 | doi = 10.1016/j.abb.2004.02.019 }}
8. ^{{cite book | vauthors = Cooper GM | title = The Cell: A Molecular Approach. | edition = 2nd | location = Sunderland (MA) | publisher = Sinauer Associates | date = 2000 | chapter = Cell-Cell Interactions | chapter-url = https://www.ncbi.nlm.nih.gov/books/NBK9851/ }}
9. ^{{cite book|url=https://books.google.com/books?id=8UZK1GZOWtYC&pg=PA66 |title=Carbohydrate Recognition: Biological Problems, Methods, and Applications |last=Wang |first=Binghe |last2=Boons |first2=Geert-Jan | name-list-format = vanc |date=2011-09-09 |publisher=John Wiley & Sons |isbn=9781118017579 |pages=66 }}
10. ^{{cite journal | vauthors = Erb IH | title = Blood Group Classification: A Plea for Uniformity | journal = Canadian Medical Association Journal | volume = 42 | issue = 5 | pages = 418–21 | date = May 1940 | pmid = 20321693 | pmc = 537907 }}
11. ^1 {{cite journal | vauthors = Neufeld EF, Hall CW | title = Formation of galactolipids by chloroplasts | journal = Biochemical and Biophysical Research Communications | volume = 14 | issue = 6 | pages = 503–8 | date = January 1964 | pmid = 5836548 | doi = 10.1016/0006-291X(64)90259-1 }}
12. ^{{cite journal | vauthors = Harwood JL, Nicholls RG | title = The plant sulpholipid-- a major component of the sulphur cycle | journal = Biochemical Society Transactions | volume = 7 | issue = 2 | pages = 440–7 | date = April 1979 | pmid = 428677 | doi = 10.1042/bst0070440 }}
13. ^{{cite journal|authorlink1=Sen-itiroh Hakomori | vauthors = Hakomori S, Igarashi Y | title = Functional role of glycosphingolipids in cell recognition and signaling | journal = Journal of Biochemistry | volume = 118 | issue = 6 | pages = 1091–103 | date = December 1995 | pmid = 8720120 | doi = 10.1093/oxfordjournals.jbchem.a124992 }}
14. ^{{cite journal | vauthors = Jurevics H, Hostettler J, Muse ED, Sammond DW, Matsushima GK, Toews AD, Morell P | title = Cerebroside synthesis as a measure of the rate of remyelination following cuprizone-induced demyelination in brain | journal = Journal of Neurochemistry | volume = 77 | issue = 4 | pages = 1067–76 | date = May 2001 | pmid = 11359872 | doi = 10.1046/j.1471-4159.2001.00310.x }}
15. ^{{cite journal | vauthors = Ariga T, McDonald MP, Yu RK | title = Role of ganglioside metabolism in the pathogenesis of Alzheimer's disease--a review | journal = Journal of Lipid Research | volume = 49 | issue = 6 | pages = 1157–75 | date = June 2008 | pmid = 18334715 | pmc = 2386904 | doi = 10.1194/jlr.R800007-JLR200 }}
16. ^{{cite journal | vauthors = Paulick MG, Bertozzi CR | title = The glycosylphosphatidylinositol anchor: a complex membrane-anchoring structure for proteins | journal = Biochemistry | volume = 47 | issue = 27 | pages = 6991–7000 | date = July 2008 | pmid = 18557633 | pmc = 2663890 | doi = 10.1021/bi8006324 }}

External links

  • {{MeshName|Glycolipids}}
{{Sphingolipids}}{{Glycolipid metabolism}}{{Authority control}}

2 : Carbohydrate chemistry|Glycolipids
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