Dynamics of tRNAtyr probed with long-lifetime metal-ligand complexes.
J Fluoresc
; 21(1): 231-7, 2011 Jan.
Article
em En
| MEDLINE
| ID: mdl-20730479
ABSTRACT
The metal-ligand complexes, [Ru(bpy)(2)(dppz)](2+) (bpy = 2,2'-bipyridine, dppz = dipyrido[3,2-a2',3'-c]phenazine) (RuBD) and [Ru(phen)(2)(dppz)](2+) (phen = 1,10-phenanthroline) (RuPD), display favorable photophysical properties including long lifetime, polarized emission, and very little background fluorescence. To check if RuBD and RuPD reflect the overall rotational mobility of small nucleic acid, we measured the intensity and anisotropy decays of RuBD and RuPD when intercalated into tRNA(tyr) using pBC SK(+) phagemid as a control. We used frequency-domain fluorometry with a blue light-emitting diode (LED) as the modulated light source. We observed shorter lifetimes for tRNA(tyr) than those for the pBC SK(+) phagemid for both probes, however, RuPD showed much larger decrease in the mean lifetime values (64%). The slow rotational correlation time of RuBD (31.3 ns) and the fast rotational correlation time of RuPD (26.0 ns) reflected the overall rotational mobility of tRNA(tyr). In addition, the steady-state anisotropy and time-resolved anisotropy decay data showed a clear difference between tRNA(tyr) and pBC SK(+) phagemid. This suggests the possibility of a homogeneous assay for identifying target nucleic acids and/or nucleic acid binding proteins.
Texto completo:
1
Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
RNA de Transferência de Tirosina
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Sondas Moleculares
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Metais
Idioma:
En
Revista:
J Fluoresc
Ano de publicação:
2011
Tipo de documento:
Article