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6,7-dimethyllumazine As A Potential Ligand For Selective Recognition Of Adenine Opposite An Abasic Site In Dna Duplexes

机译:6,7-二甲基鲁嗪作为潜在的配体,选择性识别在Dna双链体中与一个碱性位点相对的腺嘌呤

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摘要

6,7-Dimethyllumazine more selectively binds to adenine (A) base opposite the abasic site in DNA duplexes (5'-TCC AGX GCA AC-3'/3'-AGG TCN CGT TG-5', X = AP site (Spacer C3), N = A, T, C and G) than the other three nucleobases with a dissociation constant K_d of ca. 1.0 μM; substituted methyl groups enhance the binding affinity to A and the selectivity for A over T, compared to the parent molecule, lumazine.rnSingle nucleotide polymorphisms (SNPs) are extremely important as a genetic marker for the identification of disease genes and detection of genetic mutations. Thus, simple and quick detection of SNPs is a key issue in today's chemical biology, biotechnology, medicine and pharmacogenomics.
机译:6,7-二甲基鲁嗪在DNA双链体中与无碱基位点相反的腺嘌呤(A)碱基上更具选择性地结合(5'-TCC AGX GCA AC-3'/ 3'-AGG TCN CGT TG-5',X = AP位点(垫片C3),N = A,T,C和G),而解离常数K_d为ca的其他三个核碱基。 1.0μM;与母体分子lumazine相比,取代的甲基增强了与A的结合亲和力和对A的选择性。作为鉴定疾病基因和检测基因突变的遗传标记,单核苷酸多态性(SNP)极为重要。因此,简单和快速检测SNP是当今化学生物学,生物技术,医学和药物基因组学的关键问题。

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