Using Chemical Synthesis To Study and Apply Protein Glycosylation

Biochemistry. 2018 Jan 30;57(4):413-428. doi: 10.1021/acs.biochem.7b01055. Epub 2018 Jan 16.

Abstract

Protein glycosylation is one of the most common post-translational modifications and can influence many properties of proteins. Abnormal protein glycosylation can lead to protein malfunction and serious disease. While appreciation of glycosylation's importance is growing in the scientific community, especially in recent years, a lack of homogeneous glycoproteins with well-defined glycan structures has made it difficult to understand the correlation between the structure of glycoproteins and their properties at a quantitative level. This has been a significant limitation on rational applications of glycosylation and on optimizing glycoprotein properties. Through the extraordinary efforts of chemists, it is now feasible to use chemical synthesis to produce collections of homogeneous glycoforms with systematic variations in amino acid sequence, glycosidic linkage, anomeric configuration, and glycan structure. Such a technical advance has greatly facilitated the study and application of protein glycosylation. This Perspective highlights some representative work in this research area, with the goal of inspiring and encouraging more scientists to pursue the glycosciences.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Review

MeSH terms

  • Amino Acid Sequence
  • Forecasting
  • Glycopeptides / chemical synthesis
  • Glycoproteins / chemical synthesis*
  • Glycosylation
  • Humans
  • Hydrophobic and Hydrophilic Interactions
  • Models, Molecular
  • Mutagenesis, Site-Directed
  • Polysaccharides / chemistry
  • Protein Conformation
  • Protein Engineering / methods*
  • Protein Processing, Post-Translational*
  • Protein Stability

Substances

  • Glycopeptides
  • Glycoproteins
  • Polysaccharides