Dinucleotide cap analogue affinity resins for purification of proteins that specifically recognize the 5′ end of mRNA

Here we present first dinucleotide affinity resins for purification of proteins that specifically recognize the 5′ end of mRNA. Constructed resins possess either a naturally occurring mono- or trimethylated cap or their analogues resistant towards enzymatic degradation, bearing a CH2 bridge between β and γ position of the 5′,5′-triphosphate chain. All cap analogues were attached to a polymer support (EAH–Sepharose) through the carboxylic group that had been generated by derivatization of the 2′,3′-cis diol of the second nucleotide in the cap structure with levulinic acid.

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