Elżbieta Sochacka's Research Group

 

          

 

Contact


E-mail: grazyna.leszczynska@.p.lodz.pl

ORCID: https://orcid.org/0000-0002-6874-022X

 

Publications


Synthesis of Nucleobase-Modified RNA Oligonucleotides by Post-Synthetic Approach.

 

Bartosik, K., Debiec, K., Czarnecka, A., Sochacka, E., Leszczynska, G. Molecules 202025(15), 3344

 

 

C5-Substituted 2-Selenouridines Ensure Efficient Base Pairing with Guanosine; Consequences for Reading the NNG-3' Synonymous mRNA Codons.

Leszczynska, G., Cypryk, M., Gostynski, B., Sadowska, K., Herman. P., Bujacz, G., Lodyga-Chuscinska, E., Sochacka, E., Nawrot, B. Int. J. Mol. Sci. 2020, 21(8), 2882.

 

Chemical Synthesis of Oligoribonucleotide (ASL of tRNA Lys T. brucei) Containing a Recently Discovered Cyclic Form of 2-Methylthio-N 6 -threonylcarbamoyladenosine (ms2ct6A).

 

Debiec, K., Matuszewski, M., Podskoczyj, K., Leszczynska, G., Sochacka, E.  E. Chem. Eur. J. 2019, 25(58)13309-13317.

 

Escherichia coli tRNA 2-selenouridine synthase (SeIU) converts S2U-RNA to Se2U-RNA via S-geranylated-intermediate.

Sierant, M., Leszczynska, G., Sadowska, K., Komar, P., Radzikowska-Cieciura, E., Sochacka, E., Nawrot, B. FEBS Lett. 2018, 592(13), 2248-2258.

 

Reaction of S-geranyl-2-thiouracil modified oligonucleotides with alkyl amines leads to the N2-alkyl isocytosine derivatives.

Leszczynska, G., Sadowska, K., Sierant, M., Sobczak, M., Nawrot, B., Sochacka, E. Org. Biomol. Chem. 201715(25), 5332-5336.

 

C5-substituents of uridines and 2-thiouridines present at the wobble position of tRNA determine the formation of their keto-enol or zwitterionic forms - a factor important for accuracy of reading of guanosine at the 3 '-end of the mRNA codons.

Sochacka, E., Lodyga-Chruscinska, E., Pawlak, J., Cypryk, M., Bartos, P., Ebenryter-Olbinska, K., Leszczynska, G., Nawrot, B. Nucleic Acids Res. 201745(8), 4825-4836.

 

Post-synthetic conversion of 5-pivaloyloxymethyluridine present in a support-bound RNA oligomer into biologically relevant derivatives of 5-methyluridine.

Bartosik, K., Sochacka, E., Leszczynska, G. Org. Biomol. Chem. 201715(9), 2097-2103.

 

S-Geranyl-2-thiouridine wobble nucleosides of bacterial tRNAs; chemical and enzymatic synthesis of S-geranylated-RNAs and their physicochemical characterization.

Sierant, M., Leszczynska, G., Sadowska, K., Dziergowska, A., Rozanski, M., Sochacka, E., Nawrot, B., Nucleic Acids Res. 201644(22), 10986-10998.

 

Nucleoside modifications in the regulation of gene expression: focus on tRNA.

Duechler, M., Leszczynska, G., Sochacka, E., Nawrot, B, Cell Mol Life Sci. 201673(16), 3075-3095.

 

S-Geranylated 2-Thiouridines of Bacterial tRNAs: Chemical Synthesis and Physicochemical Properties.

Leszczynska, G., Sadowska, K., Bartos, P., Nawrot, B., Sochacka, E. Eur. J. Org. Chem. 201621, 3482-3485.

 

An efficient approach for conversion of 5-substituted 2-thiouridines built in RNA oligomers into corresponding desulfured 4-pyrimidinone products.

Chwialkowska, A., Wielgus, E., Leszczynska, G., Sobczak, M., Mikolajczyk, B., Sochacka, E., Nawrot, B. Bioorg. Med. Chem. Lett. 201525(16), 3100-3104.

 

Synthesis of various substituted 5-methyluridines (xm5U) and 2-thiouridines (xm5s2U) via nucleophilic substitution of 5-pivaloyloxymethyluridine/2-thiouridine.

Bartosik, K., Leszczynska, G.,Tetrahedron Lett.201556, 6593-6597.

 

Chemical synthesis of the 5-taurinomethyl(-2-thio)uridine modified anticodon arm of the human mitochondrial tRNALeu(UUR) and tRNALys.

Leszczyńska, G., Leonczak P., Wozniak, K., Malkiewicz, A. RNA 2014,20, 938-947.

 

Site-selected incorporation of 5-carboxymethylaminomethyl(-2-thio)uridine into RNA sequences by phosphoramidite chemistry.

Leszczynska, G., Pięta, J., Wozniak, K., Malkiewicz, A. Org. Biomol. Chem. 201412, 1052-1056. 

 

Chemical synthesis of human mitochondrial tRNAlys fragment containing 5-taurinomethyl-2-thiouridine and 6-threonylcarbamoyladenosine.

Wozniak, K., Stasiak, A., Leonczak, P., Leszczynska, G., Malkiewicz, A., Coll. Czech. Chem. Commun., Symp. Series , 2014,14, 408-410.

 

mt-tRNA components: synthesis of (2-thio)uridines modified with blocked glycine/taurine moieties at C-5,1.

Leszczynska, G., Leonczak, P., Dziergowska, A., Malkiewicz, A. Nucleosides, Nucleotides and Nucleic Acids 201332, 599-616. 

 

Site-specific incorporation of 5-methylaminomethyl-2-thiouridine and 2-thiouridine(s) into RNA sequences.

Leszczynska, G., Pieta, J., Leonczak, P., Tomaszewska, A., Malkiewicz, A. Tetrahedron Lett. 201253, 1214-1217.

 

Modifications modulate anticodon loop dynamics and codon recognition of E. coli tRNAArg1,2.

Cantara, W. A., Bilbille, Y., Kim  J., Kaiser, R., Leszczynska, G., Malkiewicz, A., Agris, P. F. J. Mol. Biol.2012416, 579-597.

 

Human tRNALys3UUU is pre-Structured by natural modifications for cognate and wobble codon binding through keto-enol tautomerism.

Vendeix, F. A. P, Murphy, IV F. V., Cantara, W. A., Leszczynska, G., Gustilo, E. M., Sproat, B., Malkiewicz, A., Agris, P. F. J. Mol. Biol. 2012416, 467-485.

 

ALKBH8-mediated formation of a novel diastereomeric pair of wobble nucleosides in mammalian tRNA.

van den Born, E., Vågbø, C. B., Songe-Møller L., Leihne, V., Lien, G. F., Leszczynska, G., Malkiewicz, A., Krokan, H.E., Kirpekar, F., Klungland, A., Falnes, P.Ø. Nat. Commun. 2011, 172(2), 1-7.

 

Chemical synthesis of an RNA sequence containing 2-thiocytidine (s2C): the DY647 labelled anticodon stem and loop sequence of Staphylococcus aureus tRNAArg (s2C32, mnm5U34, t6A37).

Leszczynska, G., Pieta, J., Sproat, B., Malkiewicz, A. Tetrahedron Lett. 201152,4443-4447.

 

Functional Recognition of the Modified Human tRNA (Lys3) (UUU) Anticodon Domain by HIV's Nucleocapsid Protein and a Peptide Mimic.

Graham, W.D., Barley-Maloney, L., Stark, C.J., Kaur, A., Stolyarchuk, K., Sproat, B., Leszczynska, G., Malkiewicz, A., Safwat, N., Mucha, P., Guenther, R., Agris, P. F.  J. Mol. Biol. 2011410 (4), 698-715. 

 

Specificity of phage display selected peptides for modified anticodon stem and loop domains of tRNA.

 

Eshete, M., Marchbank, M.T., Deutscher, S.L., Sproat, B., Leszczynska, G., Malkiewicz, A., Agris, P.F. Protein J. 200726(1), 61-73. 

 

Synthesis of modified oligonucleotides for investigation of catalytic activity and substrate specificity of DNAzyme 10-23.

Sochacka, E., Leszczyńska, G., Miskiewicz, A., Frątczak, I., Smuga, D. Ann. Pol. Chem. Soc2004, 652-655.

 

Modyfikowane, katalityczne kwasy nukleinowe.

Leszczyńska, G., Sochacka, E.,  Biotechnologia, 20032(61), 165-181.

 

Synthesis and properties of uniquely modified oligoribonucleotides: yeast tRNAPhe fragments with 6-methyluridine and 5,6-dimethyluridine at site-specific positions.

Sochacka, E., Czerwinska, G., Guenther, R., Cain, R., Agris, P., Małkiewicz, A. Nucleosides & Nucleotides 200019(3), 515-522.

 

Structural and functional roles of the N1- and N3-protons of Yat tRNA’s position 39.

Yarian, C. S., Basti, M. M., Cain, R. J., Ansari, G., Guenther, R., Sochacka, E., Czerwińska, G., Małkiewicz, A., Agris, P. F. Nucleic Acids Res.199927 (17), 3543-3549.

 

Thermodynamic conribution of nucleoside modifications to yeast tRNAPhe anticodon stem loop analogs.

Agris, P. F., Guenther, R., Sochacka, E., Newman, W., Czerwinska, G., Liu, G., Ye, W., Malkiewicz, A. Acta Biochem. Pol. 199946(1), 163 -172.