The P-TEFb inhibitors DRB, seliciclib and flavopiridol release P-TEFb from the large form

Copyright information:Taken from "Inhibition of HIV-1 replication by P-TEFb inhibitors DRB, seliciclib and flavopiridol correlates with release of free P-TEFb from the large, inactive form of the complex"http://www.retrovirology.com/content/4/1/47Retrovirology 2007;4():47-47.Published onli...

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Hauptverfasser: Biglione, Sebastian, Byers, Sarah A, Price, Jason P, Nguyen, Van Trung, Bensaude, Olivier, Price, David H, Maury, Wendy
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Sprache:eng
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Zusammenfassung:Copyright information:Taken from "Inhibition of HIV-1 replication by P-TEFb inhibitors DRB, seliciclib and flavopiridol correlates with release of free P-TEFb from the large, inactive form of the complex"http://www.retrovirology.com/content/4/1/47Retrovirology 2007;4():47-47.Published online 11 Jul 2007PMCID:PMC1948018. Low-salt cytosolic extract (CE) containing the large form of P-TEFb and high-salt nuclear extracts (NE) containing the free form of P-TEFb were generated from (A) DRB-treated HeLa cells, (B) DRB treated Jurkat cells, (C) seliciclib-treated HeLa37 cells or (D) flavopiridol-treated Jurkat cells. Quantitative western blotting was performed on low salt cytosolic extracts (CE) and high-salt nuclear extracts (NE) to detect the percentage of Cdk9 and cyclin T1 present in the free and large form of the P-TEFb complex. The percent of P-TEFb in the large form of the complex (low-salt or CE) was calculated as a fraction of the total amount of P-TEFb (low-salt + high-salt P-TEFb) and plotted as a function of the concentration of P-TEFb inhibitor.
DOI:10.6084/m9.figshare.60891