Abstract
A new concept for affinity two-phase partitioning was tested. The partitioning was based on the interaction of target membranes with a primary antibody which, in turn, interacted with a biotinylated secondary antibody and NeutrAvidin-dextran in a poly(ethylene glycol)/dextran two-phase system. Caveolae selectively redistributed from the top phase to the NeutrAvidin-dextran-containing bottom phase by employing anti-caveolin as the primary antibody. This immunoaffinity approach was more selective than the established sucrose gradient centrifugation method and resulted in highly purified caveolae from Triton X-100-treated liver and lung plasma membranes. The same approach, employing other selective primary antibodies, should facilitate the purification also of other membrane fractions. © 2004 Elsevier Inc. All rights reserved.
| Original language | English |
|---|---|
| Pages (from-to) | 17-26 |
| Number of pages | 9 |
| Journal | Analytical Biochemistry |
| Volume | 331 |
| Issue number | 1 |
| Publication status | Published - 1 Aug 2004 |
Keywords
- 5′-Nucleotidase
- Avidin
- Biotin
- Caveolin
- EM
- Immunoaffinity partitioning
- Isolation
- Membrane
- Two-phase system
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