Literature DB >> 18524590

Quantitating the concentration of Py-Im polyamide-fluorescein conjugates in live cells.

Carey F Hsu1, Peter B Dervan.   

Abstract

Quantitative fluorescence-based methods have been developed to determine the nuclear concentration of polyamide-fluorescein conjugates in cell culture. Confocal laser scanning microscopy and flow cytometry techniques are utilized to plot calibration curves, from which the nuclear concentration can be interpolated. Upon treatment with polyamide, the concentration in the nucleus of live HeLa cells is calculated to be between 0.1 and 0.5microM, which is significantly lower than the 2microM dosage concentration. In contrast, the observed nuclear concentration in U251 cells is closer to the dosage concentration, indicating a cell line-specific increase in uptake for this class of compounds. Although confocal microscopy and flow cytometry generate disparate values, taken together these experiments suggest that the polyamide concentration inside the cell nucleus is lower than it is outside the cell.

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Year:  2008        PMID: 18524590      PMCID: PMC2587135          DOI: 10.1016/j.bmcl.2008.05.063

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  25 in total

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6.  Nuclear localization of pyrrole-imidazole polyamide-fluorescein conjugates in cell culture.

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8.  Sequence specific fluorescence detection of double strand DNA.

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10.  Influence of structural variation on nuclear localization of DNA-binding polyamide-fluorophore conjugates.

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  16 in total

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5.  Structural basis for cyclic Py-Im polyamide allosteric inhibition of nuclear receptor binding.

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Review 7.  Structure-based DNA-targeting strategies with small molecule ligands for drug discovery.

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8.  Solution-phase synthesis of pyrrole-imidazole polyamides.

Authors:  David M Chenoweth; Daniel A Harki; Peter B Dervan
Journal:  J Am Chem Soc       Date:  2009-05-27       Impact factor: 15.419

9.  Cyclic pyrrole-imidazole polyamides targeted to the androgen response element.

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10.  Enhancing the cellular uptake of Py-Im polyamides through next-generation aryl turns.

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