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ACS Chem Biol ; 3(6): 359-72, 2008 Jun 20.
Artigo em Inglês | MEDLINE | ID: mdl-18570355

RESUMO

Bioactive small molecules, including steroids, activate multiple signaling pathways in mammalian cells. However, current technologies cannot illuminate such multiple effects of a ligand in mammalian cells. Here, we demonstrate integrated-molecule-format multicolor systems simultaneously visualizing bifacial activities of a ligand, where estrogen receptor alpha (ERalpha) was exemplified to demonstrate the present technology. First, we developed a single-molecule-format probe emitting red bioluminescence for imaging interaction between the phosphorylated ligand binding domain of ERalpha (ER LBD) and the Src homology-2 (SH2) domain of Src. The SH2 domain-linked ER LBD was sandwiched between dissected N- and C-terminal fragments of Pyrophorus plagiophthalamus (click beetle) luciferase emitting red bioluminescence. Second, another single-molecule-format bio-luminescent probe emitting green bioluminescence was constructed to visualize intramolecular interaction between ER LBD and LXXLL motifs. Mammalian cells carrying the two probes emit red and/or green light in response to agonistic and antagonistic activities of a ligand, which correspond to its genomic and nongenomic activities, respectively. Third, the two probes were assembled to make an single-molecule-format multicolor indicator, in which all of the components for ligand sensing and multiple-light emission were integrated. The probe emitted characteristic light spectra in response to various agonists and antagonists. This is the first example where (i) protein phosphorylation was recognized with a single bioluminescent probe and (ii) bifacial activities of a ligand, either agonistic or antagonistic, were simultaneously visualized with multiple colors.


Assuntos
Células , Receptor alfa de Estrogênio , Luciferases/química , Substâncias Luminescentes/química , Medições Luminescentes/métodos , Domínios de Homologia de src/fisiologia , Quinases da Família src , Animais , Sítios de Ligação , Células/citologia , Células/metabolismo , Besouros/enzimologia , Receptor alfa de Estrogênio/análise , Receptor alfa de Estrogênio/metabolismo , Ligantes , Fosforilação , Sensibilidade e Especificidade , Quinases da Família src/análise , Quinases da Família src/metabolismo
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