Department of Chemistry & Biochemistry, University of Bern, Freiestrasse 3, CH-3012 Bern, Switzerland.
Bioorg Med Chem Lett. 2012 Jul 1;22(13):4428-30. doi: 10.1016/j.bmcl.2012.04.101. Epub 2012 May 5.
Pyrene-deoxynucleoside triphosphates (dPTPs), varying by the positioning of the aromatic system, were synthesized. Their ability to function as substrates for the Klenow fragment of Escherichia coli DNA polymerase I and the TdT polymerase was assessed. The dPTPs are all equally well tolerated by the Klenow fragment, and lead to elongation of up to 5 extra nucleotides of a ssDNA primer in a TdT-mediated reaction. The tailing efficiency of the dPTPs compares favorably to other less drastically modified dNTPs.
芘脱氧核苷三磷酸(dPTPs),通过改变芳环体系的位置而合成。评估了它们作为大肠杆菌 DNA 聚合酶 I 的 Klenow 片段和 TdT 聚合酶的底物的能力。dPTPs 都被 Klenow 片段同等耐受,并导致在 TdT 介导的反应中 ssDNA 引物延伸多达 5 个额外的核苷酸。dPTPs 的加尾效率优于其他修饰程度较低的 dNTPs。