Purification of a protein kinase from human Namalwa cells that phosphorylates topoisomerase I

A nuclear protein kinase which phosphorylates phosphoprotein 110 8.4 , recently identified as topoisomerase I, has been purified approximately 330 fold from a 10 mM Tris extract of human Namalwa cells. The kinase wás chromatographed on DEAE-Sephacel and further purified by affinity chromatography on...

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Veröffentlicht in:Biochemical and biophysical research communications 1982-12, Vol.109 (4), p.1222-1227
Hauptverfasser: Mills, John S., Busch, Harris, Durban, Egon
Format: Artikel
Sprache:eng
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Zusammenfassung:A nuclear protein kinase which phosphorylates phosphoprotein 110 8.4 , recently identified as topoisomerase I, has been purified approximately 330 fold from a 10 mM Tris extract of human Namalwa cells. The kinase wás chromatographed on DEAE-Sephacel and further purified by affinity chromatography on phosvitin-Sepharose. The protein kinase exhibited a high affinity (Km = 0.3 μM) for topoisomerase I; its affinity for phosvitin was approximately 100 fold lower (Km = 25 μM).
ISSN:0006-291X
1090-2104
DOI:10.1016/0006-291X(82)91907-6