Determination of Picomolar Concentrations of Metal Ions Using Fluorescence Anisotropy: Biosensing with a “Reagentless” Enzyme Transducer
- 15 October 1998
- journal article
- Published by American Chemical Society (ACS) in Analytical Chemistry
- Vol. 70 (22), 4717-4723
- https://doi.org/10.1021/ac980864r
Abstract
Because of their high affinity and selectivity, metalloproteins can be used as transducers in novel sensors, i.e., biosensors, for the determination of trace levels of metal ions in solution. Here, we exploit carbonic anhydrase to determine picomolar to nanomolar concentrations of free transition metal ions by fluorescence anisotropy (polarization) in a reagentless format. Carbonic anhydrase variants engineered with a cysteine replacing a residue chosen near the active site (F131C and H64C) were covalently labeled with derivatives of benzoxadiazole sulfonamide. These labeled variants exhibited changes in anisotropy up to 0.07 upon binding free Cu(II), Co(II), and Zn(II) with apparent Kd's close to the values observed with wild-type apocarbonic anhydrase. The covalent attachment of the label has significant advantages over noncovalent labels we have described previously. Furthermore, the metal ion-dependent anisotropy changes were predictable using simple theory. The results demonstrate that free transition metal ions can be determined at trace levels in aqueous solution using inexpensive instruments.Keywords
This publication has 26 references indexed in Scilit:
- Structure-Based Design of a Sulfonamide Probe for Fluorescence Anisotropy Detection of Zinc with a Carbonic Anhydrase-Based BiosensorJournal of the American Chemical Society, 1996
- Performance enhancement of fluorescence energy transfer-based biosensors by site-directed mutagenesis of the transducerJournal of Biomedical Optics, 1996
- Characterization of Metal Binding by a Designed Protein: Single Ligand Substitutions at a Tetrahedral Cys2His2 SiteBiochemistry, 1995
- Structure of native and apo carbonic anhydrase II and structure of some of its anion-ligand complexesJournal of Molecular Biology, 1992
- Conformational mobility of His-64 in the Thr-200 .fwdarw. Ser mutant of human carbonic anhydrase IIBiochemistry, 1991
- Fibre-optic oxygen sensor with the fluorescence decay time as the information carrierAnalytica Chimica Acta, 1988
- Fluorescence polarization immunoassay. Theory and experimental methodImmunochemistry, 1973
- Segmental flexibility in an antibody moleculeJournal of Molecular Biology, 1970
- Visible Absorption and Circular Dichroism Spectra of 5(4'-Sulfamylphenylazo)-8-hydroxyquinoline Bound to Carbonic Anhydrase and Alcohol Dehydrogenase.Acta Chemica Scandinavica, 1970
- Photoelectric Method for the Measurement of the Polarization of the Fluorescence of SolutionsJournal of the Optical Society of America, 1956