Separation of Peptides on HALO 2-Micron Particles

Curr Protoc Protein Sci. 2016 Aug 1:85:11.6.1-11.6.16. doi: 10.1002/cpps.12.

Abstract

Reversed-phase high-performance liquid chromatography (RP-HPLC) is of fundamental importance to the isolation and separation of peptides, proteins, and other biomolecules. Hence, there is a continuing high demand for the development of RP-HPLC stationary-phase materials with enhanced separation efficiency. HALO packing materials began the revolution in "core-shell" technology with the advantages of faster separations, higher resolution and peak capacity, high temperature stability, and rugged reliable performance compared to traditional HPLC and UHPLC. These materials are characterized by a solid core surrounded by a thin layer of porous material, and represent a technology for the future with continuing refinements. Such refinements are aided via the use of designed synthetic peptide standards during stationary-phase development. Concomitantly, such standards also enable the researcher to monitor RP-HPLC column performance and develop optimized separation protocols for peptides from a wide array of sources. © 2016 by John Wiley & Sons, Inc.

Keywords: 2.0 micron particles; anionic ion-pairing reagent; core-shell; fused-core particles; reversed-phase HPLC; separation of peptides; solid core; trifluoroacetic acid (TFA).

MeSH terms

  • Chromatography, High Pressure Liquid / methods*
  • Chromatography, Reverse-Phase / methods*
  • Hydrophobic and Hydrophilic Interactions
  • Particle Size
  • Peptides / isolation & purification*
  • Porosity
  • Proteins / isolation & purification*
  • Silicon Dioxide / chemistry
  • Surface Properties
  • Trifluoroacetic Acid / chemistry

Substances

  • Peptides
  • Proteins
  • Silicon Dioxide
  • Trifluoroacetic Acid