Modern tools for the chemical ligation and synthesis of modified peptides and proteins

Future Med Chem. 2016 Dec;8(18):2287-2304. doi: 10.4155/fmc-2016-0175. Epub 2016 Nov 22.

Abstract

The ability to improve nature's capacity by introducing modification of biological interest in proteins and peptides (P&P) is one of the modern challenges in synthetic chemistry. Due to the unfavorable pharmacokinetic properties, many native P&P are of little use as therapeutic agents. Today, few methods for the preparation of modified proteins are available. Initially introduced to realize the ligation between two standard peptidic sequences, and hence to afford native proteins, the modern chemical methodologies, in other words native chemical ligation, expressed ligation, Staudinger ligation, auxiliary mediated ligation, aldehyde capture, etc., can be virtually utilized to ligate a variety of peptidomimetic partners, allowing a systematic access to modified, unnatural large P&P.

Keywords: native chemical ligation; peptide; protein chemistry.

Publication types

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

MeSH terms

  • Molecular Structure
  • Peptides / chemical synthesis*
  • Peptides / chemistry
  • Proteins / chemical synthesis*
  • Proteins / chemistry

Substances

  • Peptides
  • Proteins