Current ideas on the significance of protein glycosylation
- PMID: 3029560
- PMCID: PMC7089454
- DOI: 10.1007/BF00230632
Current ideas on the significance of protein glycosylation
Abstract
Carbohydrate has been removed from a number of glycoproteins without major effect on the structure or enzyme activity of the protein. Thus carbohydrate has been suggested to underly a non-primary function for proteins, such as in relatively non-specific interactions with other carbohydrates or macromolecules, stabilization of protein conformation, or protection from proteolysis. This non-specific concept is consistent with both the general similarity in carbohydrate structure on very diverse glycoproteins and the frequent structural microheterogeneity of carbohydrate chains at given sites. The concept is supported in a general sense by the viability of cells whose glycosylation processes have been globally disrupted by mutation or pharmacological inhibitors. In contrast to the above observations, other studies have revealed the existence of specific, selective receptors for discrete oligosaccharide structures on glycoproteins which seem to be important for compartmentalization of the glycoprotein, or the positioning of cells on which the glycoprotein is concentrated. Sometimes multivalency in the carbohydrate-receptor interaction is crucial. There are additional possible roles for carbohydrate in the transduction of information upon binding to a receptor. The possibility of specific roles for carbohydrate is supported by the existence of numerous unique carbohydrate structures, many of which have been detected as glycoantigens by monoclonal antibodies, with unique distributions in developing and differentiated cells. This article attempts to summarize and rationalize the contradictory results. It appears that in general carbohydrate does in fact underlie only roles secondary to a protein's primary function. These secondary roles are simple non-specific ones of protection and stabilization, but often also satisfy the more sophisticated needs of spatial position control and compartmentalization in multicellular eukaryotic organisms. It is suggested that there are advantages, evolutionarily speaking, for the shared use of carbohydrate for non-specific roles and for specific roles primarily as luxury functions to be executed during the processes of cell differentiation and morphogenesis.
Similar articles
-
Different roles of individual N-linked oligosaccharide chains in folding, assembly, and transport of the simian virus 5 hemagglutinin-neuraminidase.Mol Cell Biol. 1990 May;10(5):1989-2001. doi: 10.1128/mcb.10.5.1989-2001.1990. Mol Cell Biol. 1990. PMID: 2183015 Free PMC article.
-
Retention of glucose units added by the UDP-GLC:glycoprotein glucosyltransferase delays exit of glycoproteins from the endoplasmic reticulum.J Cell Biol. 1995 Aug;130(4):771-9. doi: 10.1083/jcb.130.4.771. J Cell Biol. 1995. PMID: 7642696 Free PMC article.
-
Effect of carbohydrate position on lysosomal transport of procathepsin L.Mol Biol Cell. 1998 May;9(5):1135-47. doi: 10.1091/mbc.9.5.1135. Mol Biol Cell. 1998. PMID: 9571245 Free PMC article.
-
O-linked protein glycosylation structure and function.Glycoconj J. 1996 Feb;13(1):19-26. doi: 10.1007/BF01049675. Glycoconj J. 1996. PMID: 8785483 Review.
-
N-linked protein glycosylation in the ER.Biochim Biophys Acta. 2013 Nov;1833(11):2430-7. doi: 10.1016/j.bbamcr.2013.04.001. Epub 2013 Apr 10. Biochim Biophys Acta. 2013. PMID: 23583305 Review.
Cited by
-
Orthogonal Translation for Site-Specific Installation of Post-translational Modifications.Chem Rev. 2024 Mar 13;124(5):2805-2838. doi: 10.1021/acs.chemrev.3c00850. Epub 2024 Feb 19. Chem Rev. 2024. PMID: 38373737 Free PMC article. Review.
-
Reduced hepatic iron uptake from rat aglycotransferrin.Biol Met. 1991;4(2):90-4. doi: 10.1007/BF01135384. Biol Met. 1991. PMID: 1878281
-
Pattern expression of glycan residues in AZT-treated K562 cells analyzed by lectin cytochemistry.Mol Cell Biochem. 2007 Jun;300(1-2):29-37. doi: 10.1007/s11010-006-9343-z. Epub 2007 Apr 12. Mol Cell Biochem. 2007. PMID: 17440690
-
Synthetic substrate analogues for UDP-GlcNAc: Man alpha 1-6R beta(1-2)-N-acetylglucosaminyltransferase II. Substrate specificity and inhibitors for the enzyme.Glycoconj J. 1994 Jun;11(3):210-6. doi: 10.1007/BF00731220. Glycoconj J. 1994. PMID: 7841796
-
Chinese hamster ovary cell mutants with multiple glycosylation defects for production of glycoproteins with minimal carbohydrate heterogeneity.Mol Cell Biol. 1989 Feb;9(2):377-83. doi: 10.1128/mcb.9.2.377-383.1989. Mol Cell Biol. 1989. PMID: 2710109 Free PMC article.
References
-
- Berger EG, Buddecke E, Kamerling JP, Kobata A, Paulson JC, Vliegenthart JFG. Structure, biosynthesis and functions of glycoprotein glycans. Experientia. 1983;38:1129–1258. - PubMed
-
- Olden K, Parent JB, White SL. Carbohydrate moieties of glycoproteins. Biochim Biophys Acta. 1982;650:209–232. - PubMed
-
- Aplin JD, Hughes RC. Complex carbohydrates of the extracellular matrix. Structures, interactions and biological roles. Biochim Biophys Acta. 1982;694:375–418. - PubMed
-
- Trimble RB, Maley F, Chu FK. Glycoprotein biosynthesis in yeast. J Biol Chem. 1983;258:2562–2567. - PubMed
-
- Williams DB, Lennarz WJ. Control of asparagine-linked oligosaccharide chain processing: studies on bovine pancreatic ribonuclease B. J Biol Chem. 1984;259:5105–5114. - PubMed
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources