## Abstract By using the luminescence from binuclear complexes of Tb^III^ (**Tb~2~βL^1^** and **Tb~2~βL^2^**), phosphorylated Tyr residue in peptides was selectively detected in neutral aqueous solutions. Neither the nonβphosphorylated Tyr, pSer, pThr, nor the other phosphateβcontaining biomolecule
Terbium as a solid-state probe for RNA
β Scribed by Gene Yonuschot; Donald Helman; George Mushrush; George Vande Woude; Gerry Robey
- Publisher
- Elsevier Science
- Year
- 1978
- Weight
- 692 KB
- Volume
- 8
- Category
- Article
- ISSN
- 0006-3061
No coin nor oath required. For personal study only.
β¦ Synopsis
This paper continues previous work on the analysis of nucleic acid-terbium complexes in the solid state. The fluorescence excitation and emission spectra of the RNA-terbium(III) complex is reported. The fluorescence excitation and emission spectra of both the RNA-terbium(III) and DNA-terbium(III) complexes as trapped on millipore filters is reported. One hundred percent of the DNA combined with terbium was trapped on millipore filters. Deoxyribonucleic acid was recovered from DNA-terbium(III) complexes trapped on millipore filters using SDS-extraction. Energy transfer was shown to occur from the bases in nucleic acids to the terbium ion, whereas the actual binding of terbium to nucleic acids was due to phosphate groups. The relative fluorescence of homopolyribonucleotide-terbium complexes showed that the guanine moiety was responsible for most of the observed fluorescence. Binding studies showed an equal affinity of radioactive terbium for all the homopolyribonucleotides. The fluorescence of solid-state DNA and RNA terbium complexes was used to measure picomole quantities of DNA or RNA.
π SIMILAR VOLUMES
Amyloid fibrils are intrinsically noncrystalline, insoluble, high-molecular-weight aggregates of peptides and proteins, with considerable biomedical and biophysical significance. Solid-state NMR techniques are uniquely capable of providing high-resolution, site-specific structural constraints for am