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Luminescent Trimethoprim–Polyaminocarboxylate Lanthanide Complex Conjugates for Selective Protein Labeling and Time-Resolved Bioassays
29
Citations
18
References
2011
Year
Biomolecular ToolMolecular BiologyTime-resolved BioassaysChemical BiologyEuropium LuminescenceProtein PurificationBioanalysisAnalytical BiotechnologyProteomicsProtein ChemistryBiochemistryBioconjugationFusion ProteinsSelective Protein LabelingBio-orthogonal ChemistryBiomolecular EngineeringNatural SciencesChelate ReportersProtein EngineeringChemical Probe
Labeling proteins with long-lifetime emitting lanthanide (III) chelate reporters enables sensitive, time-resolved luminescence bioaffinity assays. Heterodimers of trimethoprim (TMP) covalently linked to various cs124-sensitized, polyaminocarboxylate chelates stably retain lanthanide ions and exhibit quantum yields of europium emission up to 20% in water. A time-resolved, luminescence resonance energy transfer (LRET) assay showed that TMP-polyaminocarboxylates bind to Escherichia coli dihydrofolate reductase (eDHFR) fusion proteins with nanomolar affinity in purified solutions and in bacterial lysates. The ability to selectively impart terbium or europium luminescence to fusion proteins in complex physiological mixtures bypasses the need for specific antibodies and simplifies sample preparation.
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