A promiscuous biotin ligase fusion protein identifies proximal and interacting proteins in mammalian cells
University of South Dakota · University of Florida · +4 more institutions
Abstract
We have developed a new technique for proximity-dependent labeling of proteins in eukaryotic cells. Named BioID for proximity-dependent biotin identification, this approach is based on fusion of a promiscuous Escherichia coli biotin protein ligase to a targeting protein. BioID features proximity-dependent biotinylation of proteins that are near-neighbors of the fusion protein. Biotinylated proteins may be isolated by affinity capture and identified by mass spectrometry. We apply BioID to lamin-A (LaA), a well-characterized intermediate filament protein that is a constituent of the nuclear lamina, an important structural element of the nuclear envelope (NE). We identify multiple proteins that associate with…
Citation impact
- FWCI
- 18.94
- Percentile
- 100%
- References
- 64
Authors
4Topics & keywords
- Biotinylation
- Biotin
- Biology
- Fusion protein
- DNA ligase
- Lamin
- Nuclear lamina
- Cell biology