Back to Search
Start Over
A non-natural amino acid for efficient incorporation into proteins as a sensitive fluorescent probe.
- Source :
-
FEBS letters [FEBS Lett] 2001 Oct 19; Vol. 507 (1), pp. 35-8. - Publication Year :
- 2001
-
Abstract
- A small and highly fluorescent non-natural amino acid that contains an anthraniloyl group (atnDap) was incorporated into various positions of streptavidin. The positions were directed by a CGGG/CCCG four-base codon/anticodon pair. The non-natural mutants were obtained in excellent yields and some of them retained strong biotin-binding activity. The fluorescence wavelength as well as the intensity of the anthraniloyl group at position 120 were sensitive to biotin binding. These unique properties indicate that the atnDap is the most suitable non-natural amino acid for a position-specific fluorescent labeling of proteins that is highly sensitive to microenvironmental changes.
- Subjects :
- Binding Sites genetics
Biotin
Escherichia coli genetics
Mutagenesis, Site-Directed
Protein Biosynthesis
Proteins genetics
Recombinant Proteins biosynthesis
Recombinant Proteins chemistry
Recombinant Proteins genetics
Spectrometry, Fluorescence
Streptavidin biosynthesis
Streptavidin chemistry
Streptavidin genetics
Amino Acids chemical synthesis
Amino Acids chemistry
Fluorescent Dyes chemical synthesis
Fluorescent Dyes chemistry
Proteins chemistry
ortho-Aminobenzoates chemical synthesis
ortho-Aminobenzoates chemistry
Subjects
Details
- Language :
- English
- ISSN :
- 0014-5793
- Volume :
- 507
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- FEBS letters
- Publication Type :
- Academic Journal
- Accession number :
- 11682055
- Full Text :
- https://doi.org/10.1016/s0014-5793(01)02935-0