The use of DODT as a non-malodorous scavenger in Fmoc-based peptide synthesis

Protein Pept Lett. 2002 Oct;9(5):379-85. doi: 10.2174/0929866023408481.

Abstract

We have synthesized a random group of peptides and performed cleavages using various cleavage cocktails including 3,6-dioxa-1,8-octanedithiol (DODT). Purity of the peptides was compared to that obtained with standard protocols for cleavage using RP-HPLC and Maldi-Tof mass spectrometry. We show that stinking thiols can be replaced by the almost odourless (DODT) without negatively affecting the purity of the end product.

MeSH terms

  • Amino Acid Sequence
  • Chromatography, High Pressure Liquid
  • Ethyl Ethers / chemistry*
  • Mass Spectrometry
  • Molecular Sequence Data
  • Odorants
  • Peptides / chemical synthesis*
  • Sulfhydryl Compounds / chemistry*

Substances

  • 3,6-dioxa-1,8-octanedithiol
  • Ethyl Ethers
  • Peptides
  • Sulfhydryl Compounds