Abstract
4'-Thio-ϟ-D-oligoribonucleotides (12 mer and 16 mer) containing a mixed base sequence were synthesized via the phosphoramidite solid support approach. These RNA analogs showed very good nuclease resistance as compared with wild-type RNA. Furthermore, 4'-thio-ϟ-D-oligoribonucleotides were shown to hybridize with a complementary DNA or RNA strand to form a duplex or with a DNA hairpin to form a triple helix. 4'-Thio-RNA binds more tightly to its complementary RNA strand than to its complementary DNA strand. A 4'-thio-RNA:RNA duplex is as stable as a 2'-O-methyl-RNA:RNA duplex. 4'-Thio-RNA, however, forms a 4'thio-RNA:DNA:DNA triplex with a stability similar to the corresponding triplex with all wild-type DNA. © 1995, Mary Ann Liebert, Inc. All rights reserved.
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CITATION STYLE
Leydier, C., Bellon, L., Barascut, J. L., Morvan, F., Rayner, B., & Imbach, J. L. (1995). 4’-Thio-RNA: Synthesis of Mixed Base 4’-Thio-Oligoribonucleotides, Nuclease Resistance, and Base Pairing Properties with Complementary Single and Double Strand. Antisense Research and Development, 5(3), 167–174. https://doi.org/10.1089/ard.1995.5.167
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