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After studying this chapter, you should be able to:

  • Explain the importance of glycoproteins in health and disease.

  • Describe the principal sugars found in glycoproteins.

  • Describe the major classes of glycoproteins (N-linked, O-linked, and GPI-linked).

  • Describe the major features of the pathways of biosynthesis and degradation of glycoproteins.

  • Explain the importance of advanced glycation end-products in causing tissue damage in diabetes mellitus.

  • Explain how many microorganisms, such as influenza virus, attach to cell surfaces via sugar chains.




The glycoproteins are proteins that contain oligosaccharide chains (glycans) covalently bound to amino acids. At least half of all eukaryotic proteins have sugars attached, so that glycosylation (the enzymic attachment of sugars) is the most frequent posttranslational modification of proteins. Many proteins also undergo reversible glycosylation with a single sugar (N-acetylglucosamine) bound to a serine or threonine residue that is also a site for reversible phosphorylation. This is an important mechanism of metabolic regulation. Nonenzymic attachment of sugars to proteins can also occur, and is referred to as glycation. This process can have serious pathological consequences (eg, in poorly controlled diabetes mellitus).


Glycoproteins are one class of glycoconjugate or complex carbohydrate—equivalent terms that are used to denote molecules containing one or more carbohydrate chains covalently linked to protein (to form glycoproteins or proteoglycans) or lipid (to form glycolipids). (Proteoglycans are discussed in Chapter 50 and glycolipids in Chapter 21.) Almost all the human plasma proteins, with the notable exception of albumin, are glycoproteins. Many proteins of cellular membranes (see Chapter 40) contain substantial amounts of carbohydrate, and many membrane proteins are anchored to the lipid bilayer by a glycan chain. A number of the blood group substances are glycoproteins, whereas others are glycosphingolipids. Many peptide hormones are glycoproteins. A major problem in cancer is metastasis (see Chapter 56) and evidence is accumulating that alterations in the structures of glycoproteins and other glycoconjugates on the surface of cancer cells are important in metastasis.




Glycoproteins occur in most organisms, from bacteria to human beings. Many viruses also contain glycoproteins, some of which play key roles in viral attachment to host cells (eg, HIV-1 and influenza A virus). The glycoproteins have a wide range of functions (Table 46–1); their carbohydrate content ranges from 1% to over 85% by weight. The glycan structures of glycoproteins change in response to signals involved in cell differentiation, normal physiology, and neoplastic transformation. This is the result of different expression patterns of glycosyltransferases under different conditions. Table 46–2 lists some of the major functions of the glycan chains of glycoproteins.

Table Graphic Jump Location
TABLE 46–1Some Functions Served by Glycoproteins

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