Fox Keith R, Webster Richard, Phelps Robin J, Fokt Izabela, Priebe Waldemar
School of Biological Sciences, University of Southampton, Bassett Crescent East, Southampton, UK.
Eur J Biochem. 2004 Sep;271(17):3556-66. doi: 10.1111/j.0014-2956.2004.04292.x.
We have used footprinting techniques on a wide range of natural and synthetic footprinting substrates to examine the sequence-selective interaction of the bis-daunorubicin antibiotic WP631 with DNA. The ligand produces clear DNase I footprints that are very different from those seen with other anthracycline antibiotics such as daunorubicin and nogalamycin. Footprints are found in a diverse range of sequences, many of which are rich in GT (AC) or GA (TC) residues. As expected, the ligand binds well to the sequences CGTACG and CGATCG, but clear footprints are also found at hexanucleotide sequences such GCATGC and GCTAGC. The various footprints do not contain any particular unique di-, tri- or tetranucleotide sequences, but are frequently contain the sequence (G/C)(A/T)(A/T)(G/C). All sequences with this composition are protected by the ligand, though it can also bind to some sites that differ from this consensus by one base pair.
我们运用足迹分析技术,在多种天然和合成的足迹分析底物上,研究双柔红霉素抗生素WP631与DNA的序列选择性相互作用。该配体产生清晰的DNase I足迹,与柔红霉素和诺加霉素等其他蒽环类抗生素所产生的足迹截然不同。足迹出现在多种不同的序列中,其中许多富含GT(AC)或GA(TC)残基。正如预期的那样,该配体与序列CGTACG和CGATCG结合良好,但在六核苷酸序列如GCATGC和GCTAGC处也发现了清晰的足迹。各种足迹并不包含任何特定的独特二核苷酸、三核苷酸或四核苷酸序列,但经常包含序列(G/C)(A/T)(A/T)(G/C)。所有具有这种组成的序列都受到该配体的保护,不过它也能结合一些与该共有序列相差一个碱基对的位点。