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. 2017 Apr 19;23(22):5210-5213.
doi: 10.1002/chem.201700514. Epub 2017 Mar 29.

Chemical synthesis of long RNAs with terminal 5'-phosphate groups

Affiliations

Chemical synthesis of long RNAs with terminal 5'-phosphate groups

Ugo Pradère et al. Chemistry. .

Abstract

Long structured RNAs are useful biochemical and biological tools. They are usually prepared enzymatically, but this precludes their site-specific modification with functional groups for chemical biology studies. One solution is to perform solid-phase synthesis of multiple RNAs loaded with 5'-terminal phosphate groups, so that RNAs can be concatenated using template ligation reactions. However, there are currently no readily available reagents suitable for the incorporation of the phosphate group into long RNAs by solid-phase synthesis. Here we describe an easy-to-prepare phosphoramidite reagent suitable for the chemical introduction of 5'-terminal phosphate groups into long RNAs. The phosphate is protected by a dinitrobenzhydryl group that serves as an essential lipophilic group for the separation of oligonucleotide by-products. The phosphate is unmasked quantitatively by brief UV irradiation. We demonstrate the value of this reagent in the preparation of a library of long structured RNAs that are site-specifically modified with functional groups.

Keywords: RNA; dinitrobenzhydryl; phosphate; phosphoramidite; photolabile protecting group.

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Figures

Figure 1
Figure 1
Structure of commercially available phosphoramidite reagents 1, 2, and 3, phosphoramidite 4, and the new dinitrobenzhydryl phosphoramidite 5.
Scheme 1
Scheme 1
Preparation of dinitrobenzhydryl phosphoramidite 5 (see the Supporting Information for details).
Scheme 2
Scheme 2
a) Synthetic procedure for the preparation of 5′‐phosphate‐capped oligoribonucleotides (BP=uracil, N4‐acetyl‐cytosine, N6‐benzoyl‐adenine, N2‐isobutyryl‐guanosine; CE=cyanoethyl; DCA=dichloroacetic acid; BTT=5‐Benzylthio‐1‐H‐tetrazole). b) Left: HPLC spectra of the crude DNB‐protected 5′‐phosphate pre‐let‐7a‐2; Right: HPLC spectra of the free 5′‐phosphate pre‐let‐7a‐2 upon 5 min irradiation at 365 nm (see the Supporting Information for details).
Figure 2
Figure 2
Secondary structures of a) U6 (psoralen/biotin) and b) Cy3/Cy5‐ACA45 as provided by Mfold Web Server.

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References

    1. Shuman S., J. Biol. Chem. 2009, 284, 17365–17369. - PMC - PubMed
    1. Romaniuk P. J., Uhlenbeck O. C., Methods Enzymol. 1983, 100, 52–59. - PubMed
    1. Chaconas G., van de Sande J. H., Methods Enzymol. 1980, 65, 75–85. - PubMed
    1. Horn T., Urdea M. S., Tetrahedron Lett. 1986, 27, 4705–4708.
    1. Nagata S., Hamasaki T., Uetake K., Masuda H., Takagaki K., Oka N., Wada T., Ohgi T., Yano J., Nucleic Acids Res. 2010, 38, 7845–7857. - PMC - PubMed

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