Abstract
Three different C5-carbohydrate-functionalized LNA uridine phosphoramidites were synthesized and incorporated into oligodeoxyribonucleotides. C5-Carbohydrate-functionalized LNA display higher affinity toward complementary DNA/RNA targets (δTm/modification up to +11.0 °C), more efficient discrimination of mismatched targets, and superior resistance against 3′-exonucleases compared to conventional LNA. These properties render C5-carbohydrate-functionalized LNAs as promising modifications in antisense technology and other nucleic acid targeting applications. © 2014 American Chemical Society.
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CITATION STYLE
Kaura, M., Guenther, D. C., & Hrdlicka, P. J. (2014). Carbohydrate-functionalized locked nucleic acids: Oligonucleotides with extraordinary binding affinity, target specificity, and enzymatic stability. Organic Letters, 16(12), 3308–3311. https://doi.org/10.1021/ol501306u
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