Abstract
Cu2+, Ni2+, Zn2+, Co2+ and Cd2+ were evaluated in metal ion affinity chromatography for enrichment of selenoprotein P, and immobilized Co2+ affinity chromatography was found to be the most selective chromatographic method. The chromatography was performed by fast protein liquid chromatography and the fractionation was followed by analysis of the collected fractions for selenium by inductively coupled plasma mass spectrometry. By the combination of immobilized Co2+ affinity chromatography and heparin affinity chromatography a simple method was developed yielding a 14,800-fold enrichment of selenoprotein P. The purity of the protein was determined by SDS-PAGE and by sequencing from polyvinylidene difluoride blots of SDS-PAGE gels.
| Original language | English |
|---|---|
| Journal | Journal of Chromatography B: Biomedical Sciences and Applications |
| Volume | 735 |
| Issue number | 1 |
| Pages (from-to) | 85-91 |
| Number of pages | 7 |
| ISSN | 1387-2273 |
| Publication status | Published - 1999 |
Keywords
- Affinity Labels
- Amino Acid Sequence
- Cadmium
- Chromatography, Affinity
- Cobalt
- Copper
- Electrophoresis, Polyacrylamide Gel
- Humans
- Metals
- Molecular Weight
- Nickel
- Proteins
- Selenoprotein P
- Selenoproteins
- Sepharose
- Zinc