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首页> 外文期刊>FEBS Letters >Modified nucleoside 5'‐triphosphates containing 2',3'‐fused threemembered rings as substrates for different DNA polymerases
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Modified nucleoside 5'‐triphosphates containing 2',3'‐fused threemembered rings as substrates for different DNA polymerases

机译:含有2',3'-融合的三元环的修饰的5'-三磷酸核苷作为不同DNA聚合酶的底物

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>5'-Triphosphates of 1-(2',3'-epithio-2',3'-dideoxy-β-D-lyxofuranosy)thymine, 1-(2',3'-epithio-2',3'-dideoxy-β-D-ribofuranosyl)thymine and 2',3'-lyxoanhydrothymidine have been shown to be termination substrates for human immunodeficiency virus (HIV) and avian myeloblastosis virus (AMV) reverse transcriptases as well as DNA polymerase I from E. coli and DNA polymerase β from rat liver. At the same time they do not terminate DNA synthesis catalysed by DNA polymerase ϵ from human placenta. Km values of ItTTP, rtTTP and laTTP incorporation into the DNA chain during catalysis by AMV reverse transcriptase agree closely with each other being 1.5–2.5 times higher than Km value for dTTP. Furthermore, Vmax values for modified substrates are only 2–3 times lower than Vmax for dTTP. The evidence favours the hypothesis of high affinity of modified nucleotides with a flattened furanosyl ring for DNA polymerase active sites.
机译:p(1-(2',3'-epithio-2',3'-二脱氧-β-D-lyxofuranosysy)胸腺嘧啶,1-(2',3'-epithio-2',3的5'-三磷酸已证明'-二脱氧-β-D-呋喃呋喃糖基)胸腺嘧啶和2',3'-lyxoanhydrothymidine是人类免疫缺陷病毒(HIV)和禽成纤维细胞病病毒(AMV)逆转录酶以及来自em> E。大鼠肝脏中的大肠杆菌和DNA聚合酶β。同时,它们不终止由人胎盘的DNA聚合酶催化的DNA合成。在AMV逆转录酶催化过程中,ItTTP,rtTTP和laTTP掺入DNA链的 K m 值彼此接近,比 K高1.5-2.5倍dTTP的 m 值。此外,修饰底物的 V max 值仅比dTTP的 V max 低2-3倍。证据支持这样的假设,即具有扁平呋喃糖基环的修饰核苷酸对DNA聚合酶活性位点具有高亲和力。

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