Abstract
The human protein C23 (nucleolin) is a major nucleolar protein. Its interactions with other proteins were studied with the two-hybrid system which identified nucleolar protein B23 (nucleophosmin) as being associated with C23. Both proteins were co-immunoprecipitated from HeLa cell nuclear extract by either monoclonal anti-C23 or monoclonal anti-B23. Binding studies utilizing deletion mutants indicated that the binding of C23 and B23 involves specific motifs. In addition to an approximately 46-amino-acid-binding domain in B23 (amino acids 194-239), amino acids 540-628 of C23 were required for binding; this region of C23 is required for the nucleolar localization. In addition, nucleolar protein p120 was also found to be co-immunoprecipitated with B23. A fragment of p120 containing a functional nucleolar localization signal bound to the truncated binding domain of B23, as did C23. These results suggest that the interaction of C23 and B23 may represent a nucleolar-targeting mechanism in which B23 acts as a nucleolar-localization signal-binding protein.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 153-158 |
| Number of pages | 6 |
| Journal | European Journal of Biochemistry |
| Volume | 237 |
| Issue number | 1 |
| DOIs | |
| State | Published - 1996 |
Keywords
- B23
- C23
- Nucleolin
- Nucleophosmin
- Protein-protein interaction
ASJC Scopus subject areas
- Biochemistry
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