reviewChemical Society ReviewsSep 16, 2008Closed access

Total chemical synthesis of proteins

University of Chicago

PubMed
Indexed incrossrefpubmed

Abstract

This tutorial review outlines the modern ligation methods that enable the efficient total chemical synthesis of enzymes and other protein molecules. Key to this success is the chemoselective reaction of unprotected synthetic peptides ('chemical ligation'). Notably, native chemical ligation enables the reaction of two unprotected peptides in aqueous solution at neutral pH to form a single product in near quantitative yield. Full-length synthetic polypeptides are folded to form the defined tertiary structure of the target protein molecule, which is characterized by mass spectrometry, NMR, and X-ray crystallography, in addition to biochemical and/or biological activity.

Citation impact

915
total citations
FWCI
21.20
Percentile
100%
References
43
Citations per year

Authors

1

Topics & keywords

Keywords
  • Native chemical ligation
  • Chemistry
  • Chemical ligation
  • Chemical synthesis
  • Molecule
  • Yield (engineering)
  • Mass spectrometry
  • Combinatorial chemistry
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