Abstract
Two chromatographic methods, capable of separating mixed peptides from contaminating amino acids in biological digests, are described. Both methods involve separation on copper-Chelex resin, but each uses a different set of elution buffers. When separation method 1 was applied to a commercially available proteolytic digest of casein, the free amino acid content was reduced from 26.0% to 0.5%. With an enzymic digest of 14C-labelled proteins derived from plant biomass, separation method 2 decreased the contaminating free amino acids from 20.3% to 1.9%. Since the separated peptides are eluted with volatile buffers, they are suitable as substrates for biological experiments
| Original language | English |
|---|---|
| Pages (from-to) | 259-263 |
| Number of pages | 5 |
| Journal | Journal of Chromatography A |
| Volume | 586 |
| Issue number | 2 |
| DOIs | |
| Publication status | Published - 22 Nov 1991 |
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