Spiral counter-current chromatography of small molecules, peptides and proteins using the spiral tubing support rotor

J Chromatogr A. 2011 Sep 9;1218(36):6148-55. doi: 10.1016/j.chroma.2011.06.007. Epub 2011 Jun 12.

Abstract

An important advance in countercurrent chromatography (CCC) carried out in open flow-tubing coils, rotated in planetary centrifuges, is the new design to spread out the tubing in spirals. More spacing between the tubing was found to significantly increase the stationary phase retention, such that now all types of two-phase solvent systems can be used for liquid-liquid partition chromatography in the J-type planetary centrifuges. A spiral tubing support (STS) frame with circular channels was constructed by laser sintering technology into which FEP tubing was placed in 4 spiral loops per layer from the bottom to the top and a cover affixed allowing the tubing to connect to flow-tubing of the planetary centrifuge. The rotor was mounted and run in a P.C. Inc. type instrument. Examples of compounds of molecular weights ranging from <300 to approximately 15,000 were chromatographed in appropriate two-phase solvent systems to assess the capability for separation and purification. A mixture of small molecules including aspirin was completely separated in hexane-ethyl acetate-methanol-water. Synthetic peptides including a very hydrophobic peptide were each purified to a very high purity level in a sec-butanol solvent system. In the STS rotor high stationary phase retention was possible with the aqueous sec-butanol solvent system at a normal flow rate. Finally, the two-phase aqueous polyethylene glycol-potassium phosphate solvent system was applied to separate a protein from a lysate of an Escherichia coli expression system. These experiments demonstrate the versatility of spiral CCC using the STS rotor.

Publication types

  • Evaluation Study
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Countercurrent Distribution / instrumentation
  • Countercurrent Distribution / methods*
  • Escherichia coli Proteins / chemistry
  • Escherichia coli Proteins / isolation & purification*
  • Hydrophobic and Hydrophilic Interactions
  • Molecular Weight
  • Peptides / chemistry
  • Peptides / isolation & purification*
  • Small Molecule Libraries / chemistry
  • Small Molecule Libraries / isolation & purification*

Substances

  • Escherichia coli Proteins
  • Peptides
  • Small Molecule Libraries