Peptide purification using the chemoselective reaction between N-(methoxy)glycine and isothiocyanato-functionalized resin

J Pept Sci. 2016 Jun;22(6):379-82. doi: 10.1002/psc.2888.

Abstract

An efficient peptide purification strategy is established, comprising the selective reaction of an N-terminal N-(methoxy)glycine residue of the peptide and isothiocyanato-functionalized resins, and subsequent Edman degradation. These reactions take place in acidic media; in particular, the Edman degradation proceeds smoothly in media containing more than 50% trifluoroacetic acid (v/v). These acidic conditions offer increased solubility, making them advantageous for the purification of hydrophobic and aggregation-prone peptides. The effectiveness of this method, together with scope and limitations, is demonstrated using model peptides and the practical purification of the loop region of the human dopamine D2 receptor long isoform (residues 240-272). Copyright © 2016 European Peptide Society and John Wiley & Sons, Ltd.

Keywords: Edman degradation; N-(methoxy)glycine; peptide purification; selective capture.

MeSH terms

  • Amino Acid Sequence
  • Combinatorial Chemistry Techniques
  • Glycine / chemistry*
  • Humans
  • Isothiocyanates / chemistry*
  • Peptides / chemistry
  • Peptides / isolation & purification*
  • Receptors, Dopamine D2 / chemistry*
  • Trifluoroacetic Acid / chemistry

Substances

  • DRD2 protein, human
  • Isothiocyanates
  • Peptides
  • Receptors, Dopamine D2
  • Trifluoroacetic Acid
  • Glycine