Selection-based discovery of macrocyclic peptides for the next generation therapeutics

Curr Opin Chem Biol. 2015 Jun:26:34-41. doi: 10.1016/j.cbpa.2015.01.023. Epub 2015 Feb 20.

Abstract

Naturally occurring macrocyclic peptides represent a unique class of compounds that exhibit various biological activities ranging from antibiotics to immunosuppressant. Although the discovery of such macrocyclic peptides had relied on their isolation from living organisms, recent advances in ribosomal peptide synthesis and in display techniques made it possible to use artificially generated macrocyclic peptide libraries for selection of ligands for biologically relevant proteins. In this review, we discuss the technologies and their applications for the discovery of peptide ligands.

Publication types

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

MeSH terms

  • Cyclization
  • Drug Discovery*
  • Gene Expression Profiling / methods
  • Humans
  • Hydrocarbons, Brominated / chemistry
  • Ligands
  • Models, Molecular
  • Peptide Library*
  • Peptides, Cyclic / biosynthesis
  • Peptides, Cyclic / chemistry
  • Peptides, Cyclic / isolation & purification*
  • Protein Biosynthesis
  • Ribosomes / genetics
  • Sirtuin 2 / antagonists & inhibitors
  • Sirtuin 2 / chemistry
  • Succinimides / chemistry

Substances

  • Hydrocarbons, Brominated
  • Ligands
  • Peptide Library
  • Peptides, Cyclic
  • Succinimides
  • alpha,alpha'-dibromoxylene
  • disuccinimidyl glutarate
  • SIRT2 protein, human
  • Sirtuin 2