Wagenknecht Hans-Achim
University of Regensburg, Institute for Organic Chemistry, D-93040 Regensburg, Germany.
Ann N Y Acad Sci. 2008;1130:122-30. doi: 10.1196/annals.1430.001. Epub 2007 Dec 20.
There is an increasing need for fluorescent nucleic acid probes that are able to sense genetic variations without the application of enzymes. The incorporation of organic fluorophores either as DNA base modifications or as DNA base substitutions represents a powerful and versatile method for such new fluorescent DNA assays. Multiple labeling of oligonucleotides using several adjacent chromophore-modified DNA bases yields fluorescence enhancement and modulation that are sensitive to single-base mismatches in the complementary oligonucleotide. Charge transfer processes that cause fluorescence quenching are DNA-base mediated and occur over several base pairs distance. Our "DETEQ" setup, consisting of a fluorescence DNA base substitution and the charge acceptor as a second modification two base pairs away, allows the homogeneous detection of single-base mutations simply by fluorescence readout. This could lead to new DNA microarrays which are based on charge transfer processes and can be analyzed by commonly used fluorescence readout techniques.
对无需酶参与就能检测基因变异的荧光核酸探针的需求日益增长。将有机荧光团作为DNA碱基修饰或DNA碱基替代物掺入,是用于此类新型荧光DNA检测的一种强大且通用的方法。使用几个相邻的发色团修饰DNA碱基对寡核苷酸进行多重标记,会产生对互补寡核苷酸中单碱基错配敏感的荧光增强和调制。导致荧光猝灭的电荷转移过程是由DNA碱基介导的,且发生在几个碱基对的距离上。我们的“DETEQ”装置由一个荧光DNA碱基替代物和两个碱基对之外作为第二种修饰的电荷受体组成,通过荧光读数就能简单地实现对单碱基突变的均相检测。这可能会催生基于电荷转移过程且能用常用荧光读数技术进行分析的新型DNA微阵列。