Displacement chromatography of proteins was successfully carried out in bot
h hydrophobic interaction and reversed-phase chromatographic systems using
low-molecular weight displacers. The displacers employed for hydrophobic di
splacement chromatography were water soluble, charged molecules containing
several short alkyl and/or aryl groups. Spectroscopy was employed to verify
the absence of structural changes to the proteins displaced on these hydro
phobic supports. Displacement chromatography on a reversed-phase material w
as employed to purify a growth factor protein from its closely related vari
ants, demonstrating the high resolutions that can be achieved by hydrophobi
c displacement chromatography. This process combines the high-resolution/hi
gh-throughput characteristics of displacement chromatography with the uniqu
e selectivity of these hydrophobic supports and offers the chromatographic
engineer a powerful tool for the preparative purification of proteins. (C)
2000 John Wiley & Sons, Inc.