This master’s thesis is part of the study focused on elucidating the structural properties of oligonucleotides with different numbers of d(ATTTC) repeats by means of NMR spectroscopy, CD spectroscopy and natural polyacrylamide gel electrophoresis. The d(ATTTC) repeats have been linked to spinocerebellar ataxia type 37 and adult myoclonic epilepsy. Transcription of d(ATTTC) repeats lead to the accumulation of RNA in the cell, which sequester RNA-binding proteins, thereby hindering their normal functions. With the help of the spectroscopic analysis we demonstrated that folding of all studied oligonucleotides depends on the presence of Mg2+ and Ca2+ cations in solution. We focused on studying the oligonucleotide with three d(ATTTC) repeats denominated ‘EP3’, which exhibits most amenable dispersion of 1H NMR signals in terms of detail structural analysis. The results of this master's work include characterization of EP3 that were crucial for the subsequent determination of its high-resolution structure. With the help of 13C- and 15N-isotopic labelling of individual nucleotides and the use of the 2D NMR methods, we assigned most of the observed NOE signals, which enabled detailed insights into the structure adopted by EP3 in the presence of Mg2+ cations. Furthermore, we found that the structure consists of two oligonucleotidesconnected via two C-C+ and two T-T base pairs. The latter represents the central part of the dimeric structure, in which each of the oligonucleotides comprises a segment that forms two A-T base pairs connected by a trinucleotide loop. Analysis of oligonucleotides with two or more than three d(ATTTC) repeats revealed an equilibrium of different DNA structures. Detailed structural characterization of individual species in equilibrium is aggravated mainly due to broad 1H NMR signals that are overlapped. Nevertheless, based on the results of CD and NMR spectroscopic analysis, we can conclude that the structural properties of all studied oligonucleotides are at least partially similar and contain the same secondary structural motifs.
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