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1.
J Am Chem Soc ; 124(32): 9344-5, 2002 Aug 14.
Artigo em Inglês | MEDLINE | ID: mdl-12167008

RESUMO

While most biotin-fluorophore conjugates suffer from significant emission quenching upon binding to avidin due to resonance energy-transfer, three novel rhenium(I) polypyridine biotin complexes have been designed in view of their characteristic photophysical properties, in particular their large Stokes shifts. In contrast to most biotin-fluorophore conjugates, the (3)MLCT emission intensities and lifetimes of these rhenium(I) complexes are increased upon binding to avidin, rendering them luminescent probes for avidin and biotinylated species.


Assuntos
Avidina/metabolismo , Biotina/química , Piridinas/química , Rênio/química , Biotina/metabolismo , Medições Luminescentes , Ligação Proteica , Piridinas/metabolismo , Rênio/metabolismo
2.
Inorg Chem ; 41(1): 40-6, 2002 Jan 14.
Artigo em Inglês | MEDLINE | ID: mdl-11782142

RESUMO

We report the synthesis, characterization, and photophysical properties of a series of rhenium(I) polypyridine maleimide complexes [Re(N-N)(CO)(3)(py-3-mal)](CF(3)SO(3)) [N-N = 1,10-phenanthroline, phen (1), 2,9-dimethyl-1,10-phenanthroline, 2,9-Me(2)-phen (2), 3,4,7,8-tetramethyl-1,10-phenanthroline, 3,4,7,8-Me(4)-phen (3), 4,7-diphenyl-1,10-phenanthroline, 4,7-Ph(2)-phen (4), 2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline, 2,9-Me(2)-4,7-Ph(2)-phen (5), 2,2'-biquinonine, biq (6); py-3-mal = N-(3-pyridyl)maleimide]. The X-ray crystal structure of complex 2 has been investigated. Upon excitation, the complexes exhibit intense and long-lived photoluminescence in fluid solutions at 298 K. The emission wavelengths range from 514 to 654 nm, and the emission lifetimes fall in the microsecond time scale. The luminescence is assigned to originate from a metal-to-ligand charge-transfer MLCT [dpi(Re) --> pi*(diimine)] triplet excited state. As the maleimide group can react with the sulfhydryl group to form a stable thioether moiety, these complexes have been used as thiol-specific luminescent labels for a thiolated oligonucleotide, glutathione, and bovine serum albumin and human serum albumin. The photoluminescence properties of the labeled biological species have also been investigated.


Assuntos
Maleimidas/química , Maleimidas/síntese química , Compostos Organometálicos/química , Compostos Organometálicos/síntese química , Piridinas/química , Piridinas/síntese química , Rênio/química , Compostos de Sulfidrila/química , Animais , Sequência de Bases , Bovinos , Cristalografia por Raios X , Polarização de Fluorescência , Glutationa/química , Humanos , Ligantes , Espectroscopia de Ressonância Magnética , Maleatos/química , Conformação Molecular , Dados de Sequência Molecular , Estrutura Molecular , Fotoquímica , Albumina Sérica/química , Soroalbumina Bovina/química , Espectrometria de Massas por Ionização por Electrospray , Espectrofotometria Infravermelho , Espectrofotometria Ultravioleta , Tionucleotídeos/química
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