Ca2(+)-dependent interaction of N-copine, a member of the two C2 domain protein family, with OS-9, the product of a gene frequently amplified in osteosarcoma

FEBS Lett. 1999 Jun 18;453(1-2):77-80. doi: 10.1016/s0014-5793(99)00700-0.

Abstract

N-copine is a novel two C2 domain protein that shows Ca2(+)-dependent phospholipid binding and membrane association. By using yeast two-hybrid assays, we identified OS-9 as a protein capable of interacting with N-copine. We further revealed that the second C2 domain of N-copine bound with the carboxy-terminal region of OS-9. Their interaction in vivo was also confirmed by co-immunoprecipitation from 293E cells co-expressing transfected N-copine and OS-9. In vitro binding assays showed that this interaction was Ca2(+)-dependent. By Northern blot analysis, N-copine and OS-9 were co-expressed in the same regions of human brain. These results reveal that OS-9 is a potential target of N-copine.

MeSH terms

  • Binding Sites
  • Brain Chemistry
  • Calcium / metabolism*
  • Carrier Proteins / genetics
  • Carrier Proteins / isolation & purification
  • Carrier Proteins / metabolism*
  • Cloning, Molecular
  • Gene Amplification
  • Humans
  • Lectins
  • Neoplasm Proteins / genetics
  • Neoplasm Proteins / isolation & purification
  • Neoplasm Proteins / metabolism*
  • Osteosarcoma
  • Protein Binding
  • Saccharomyces cerevisiae / genetics
  • Tissue Distribution

Substances

  • Carrier Proteins
  • Lectins
  • Neoplasm Proteins
  • OS9 protein, human
  • copine
  • Calcium