- Postsynthetic conjugation of RNA to carboxylate and dicarboxylate molecules.
Postsynthetic conjugation of RNA to carboxylate and dicarboxylate molecules.
Nucleosides, nucleotides & nucleic acids (2015-10-01)
Yossi Shemesh, Eylon Yavin
PMID26422297
RÉSUMÉ
Carboxylates and dicarboxylates are important phosphate mimics. Herein, we present a simple synthetic route for the preparation of RNA carboxylate/dicarboxylate conjugates, starting from suitably protected NH2- and COOH-containing molecules that are coupled to the RNA on the solid support. The key point in our method was the use of trimethylsilylethanol (TMSE-OH) protecting group, which is removed simultaneously with the silyl protecting group on the 2'-OH of the RNA ribose (e.g. t-Butyldimethylsilyl) during the final RNA cleavage/deprotection steps. The usefulness of this method was demonstrated by preparing different RNA-phosphate mimics oligos.
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Acide chlorhydrique, meets analytical specification of Ph. Eur., BP, NF, fuming, 36.5-38%
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Acide chlorhydrique, puriss. p.a., ACS reagent, reag. ISO, reag. Ph. Eur., fuming, ≥37%, APHA: ≤10
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Éthanol, purum, absolute ethanol, denaturated with 4.8% isopropanol, A15 IPA1, ≥99.8% (based on denaturant-free substance)
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Palladium hydroxide on carbon, extent of labeling: 20 wt. % loading (dry basis), matrix carbon, wet support