Synthesis of hydrophilic and flexible linkers for peptide derivatization in solid phase

Bioorg Med Chem Lett. 2004 Jan 5;14(1):161-5. doi: 10.1016/j.bmcl.2003.09.067.

Abstract

Four N-Fmoc protected polyoxyethylene-based amino acid type linkers were designed and synthesized for peptide derivatization in solid phase. Three of them were obtained in a crystalline form. The crystallized linkers can be stored at 4 degrees C for 2 years without significant decomposition. Protocols for biotinylation and fluorescent labeling of peptides in solid phase were developed. The linkers also provide good ionization ability for single-bead mass spectrometry analysis of peptides.

Publication types

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

MeSH terms

  • Biotinylation
  • Chromatography, High Pressure Liquid
  • Combinatorial Chemistry Techniques
  • Nuclear Magnetic Resonance, Biomolecular
  • Peptides / chemical synthesis*
  • Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization

Substances

  • Peptides