Are you an EPFL student looking for a semester project?
Work with us on data science and visualisation projects, and deploy your project as an app on top of Graph Search.
The prepn. and the pairing properties of the new 3'-deoxyribopyranose (4'->2')-oligonucleotide (= p-DNA) pairing system, based on 3'-deoxy-b-D-ribo-pyranose nucleosides is presented. D-Xylose was efficiently converted to the prefunctionalized 3-deoxyribopyranose deriv. 4-O-[(tert-butyl)dimethylsilyl]-3-deoxy-D-ribo-pyranose 1,2-diacetate (obtained as a 4:1 mixt. of a- and b-D-anomers). From this sugar building block, the corresponding, appropriately protected thymine, guanine, 5-methylcytosine, and purine-2,6-diamine nucleoside phosphoramidites were prepd. in a minimal no. of steps. These building blocks were assembled on a DNA synthesizer, and the corresponding p-DNA oligonucleotides were obtained in good yields after a one-step deprotection under std. conditions, followed by HPLC purifn. Qual., p-DNA shows the same pairing behavior as p-RNA, forming antiparallel, exclusively Watson-Crick-paired duplexes that are much stronger than corresponding DNA duplexes. Duplex stabilities within the three related (i.e., based on ribo-pyranose nucleosides) oligonucleotide systems p-RNA, p-DNA, and 3'-O-Me-p-RNA were compared with each other. Intrinsically, p-RNA forms the strongest duplexes, followed by p-DNA, and 3'-O-Me-p-RNA. However, by introducing the nucleobases purine-2,6-diamine and 5-methylcytosine instead of adenine and cytosine, a substantial increase in stability of corresponding p-DNA duplexes was obsd. [on SciFinder (R)]
Francesco Stellacci, Weina Liu, Yong Zhu