RESUMO
Individual mammalian cells exhibit large variability in cellular volume, even with the same absolute DNA content, and so must compensate for differences in DNA concentration in order to maintain constant concentration of gene expression products. Using single-molecule counting and computational image analysis, we show that transcript abundance correlates with cellular volume at the single-cell level due to increased global transcription in larger cells. Cell fusion experiments establish that increased cellular content itself can directly increase transcription. Quantitative analysis shows that this mechanism measures the ratio of cellular volume to DNA content, most likely through sequestration of a transcriptional factor to DNA. Analysis of transcriptional bursts reveals a separate mechanism for gene dosage compensation after DNA replication that enables proper transcriptional output during early and late S phase. Our results provide a framework for quantitatively understanding the relationships among DNA content, cell size, and gene expression variability in single cells.
Assuntos
Dosagem de Genes , Hibridização in Situ Fluorescente/métodos , Análise de Sequência de RNA/métodos , Análise de Célula Única/métodos , Transcrição Gênica , Animais , Caenorhabditis elegans/genética , Células Cultivadas , Fibroblastos/citologia , Prepúcio do Pênis/citologia , Expressão Gênica , Humanos , Masculino , Dados de Sequência Molecular , Fase SRESUMO
We report narrow-band absorption enhancement of semiconductor nanocrystals via Förster resonance energy transfer from cyanine J-aggregates. These J-aggregated dyes associate electrostatically with short quantum-dot (QD) surface ligands in solution. Energy transfer efficiencies approach unity for this light sensitization and result in a 5-fold enhancement in the QD excitation near the J-aggregate absorption maximum. Because a thin layer of J-aggregates attenuates the same amount of light (at peak absorbance) as a far thicker film of monomer dye, these absorption-enhanced materials may have applications in light-sensitizing applications such as photodetection and optical down-conversion.
Assuntos
Pontos Quânticos , Adsorção , Carbocianinas/química , Coloides , Transferência Ressonante de Energia de Fluorescência , Ligantes , Nanopartículas , Semicondutores , Eletricidade Estática , Fatores de TempoRESUMO
We demonstrate reversible quenching of the photoluminescence from single CdSe/ZnS colloidal quantum dots embedded in thin films of the molecular organic semiconductor N,N'-diphenyl-N,N'-bis(3-methylphenyl)-(1,1'-biphenyl)-4,4'-diamine (TPD) in a layered device structure. Our analysis, based on current and charge carrier density, points toward field ionization as the dominant photoluminescence quenching mechanism. Blinking traces from individual quantum dots reveal that the photoluminescence amplitude decreases continuously as a function of increasing forward bias even at the single quantum dot level. In addition, we show that quantum dot photoluminescence is quenched by aluminum tris(8-hydroxyquinoline) (Alq3) in chloroform solutions as well as in thin solid films of Alq3 whereas TPD has little effect. This highlights the importance of chemical compatibility between semiconductor nanocrystals and surrounding organic semiconductors. Our study helps elucidate elementary interactions between quantum dots and organic semiconductors, knowledge needed for designing efficient quantum dot organic optoelectronic devices.
Assuntos
Coloides/química , Compostos Orgânicos/química , Semicondutores , Diaminas/química , Luminescência , Teoria QuânticaRESUMO
We have developed a photostable nanocrystal-silica (NC-silica) laser that is robust under different chemical environments, making it suitable for integration with a microfluidic network. We demonstrate that the optical properties of this microscale laser can be a dynamic function of its local environment, thus providing a platform for potential applications such as nonlinear optical chemosensing on a miniaturized scale.