26 results on '"Oretskaya, Tatiana S."'
Search Results
2. Atomic force microscopy characterization of synthetic pyrimidinic oligodeoxynucleotides adsorbed onto an HOPG electrode under applied potential
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Chiorcea Paquim, Ana-Maria, Oretskaya, Tatiana S., and Oliveira Brett, Ana Maria
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ATOMIC force microscopy , *SEPARATION (Technology) , *SCANNING probe microscopy , *NUCLEIC acids - Abstract
Abstract: In order to better understand the adsorption mechanism of nucleic acids at electrode surface, MAC Mode atomic force microscopy (MAC Mode AFM) was used to investigate the adsorption of a 10-base synthetic oligodeoxynucleotide (ODN) with the sequence 5′-CTTTTTCTTT-3′ containing only pyrimidinic bases, onto a highly oriented pyrolytic graphite (HOPG) electrode. Free adsorption and adsorption at applied potentials of +0.30 and +0.65V versus AgQRE, were carried out. AFM images in air demonstrated that the molecules adsorb spontaneously on the electrode surface. The ODNs have the tendency to self-assemble from solution onto the solid support in a tight and well-spread two-dimensional lattice covering the entire surface, showing the existence of different molecular conformations and exposing parts of the HOPG surface. The degree of surface coverage and the adsorption pattern were directly dependent on ODN concentration and immobilization procedure. During free adsorption, the hydrophobic interactions of the ODNs with the HOPG represent the main adsorption mechanism. When a positive potential is applied to the HOPG, electrostatic interactions between the positively charged electrode surface and the negatively charged sugar-phosphate backbones of ODNs are predominant. [Copyright &y& Elsevier]
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- 2006
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3. Adsorption of synthetic homo- and hetero-oligodeoxynucleotides onto highly oriented pyrolytic graphite: Atomic force microscopy characterization
- Author
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Chiorcea Paquim, Ana-Maria, Oretskaya, Tatiana S., and Oliveira Brett, Ana Maria
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ADSORPTION (Chemistry) , *SURFACE chemistry , *NUCLEIC acids , *DNA - Abstract
Abstract: DNA adsorption on electrode surfaces is of fundamental interest for the development of DNA-based biosensors. The free adsorption of 10-mer synthetic oligodeoxynucleotides (ODNs) onto highly oriented pyrolytic graphite (HOPG) surfaces was studied using Magnetic AC mode atomic force microscopy (MAC Mode AFM). The mechanism of interaction of nucleic acids with carbon electrode surfaces was elucidated, using 10-mer synthetic homo- and hetero-ODNs sequences of known base sequences, because they allow clear interpretation of the experimental data. AFM images in air revealed different adsorption patterns and degree of HOPG surface coverage for the ODNs, and correlation with the individual structure and base sequence of each ODN molecule will be presented. The results demonstrated that the hydrophobic interactions with the HOPG hydrophobic surface explain the main adsorption mechanism, although other effects such as electrostatic and Van der Waals interactions may contribute to the free adsorption process. The ODNs interacted differently with the HOPG surface, according to the ODN sequence hydrophobic characteristics, being directly depending on the molecular mass, the hydrophobic character of the individual bases and on the secondary structure of the molecule. The importance of the type of base existent at the ODN chain extremities on the adsorption process was investigated and different adsorption patterns were obtained with ODN sequences composed by the same group of bases aligned in a different order. [Copyright &y& Elsevier]
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- 2006
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4. Reactive Acrylamide-Modified DNA Traps for Accurate Cross-Linking with Cysteine Residues in DNA–Protein Complexes Using Mismatch Repair Protein MutS as a Model.
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Monakhova, Mayya V., Kubareva, Elena A., Kolesnikov, Kirill K., Anashkin, Viktor A., Kosaretskiy, Egor M., Zvereva, Maria I., Romanova, Elena A., Friedhoff, Peter, Oretskaya, Tatiana S., and Zatsepin, Timofei S.
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PROTEIN models , *DNA , *CYSTEINE , *DNA-protein interactions , *URIDINE , *DNA mismatch repair - Abstract
Covalent protein capture (cross-linking) by reactive DNA derivatives makes it possible to investigate structural features by fixing complexes at different stages of DNA–protein recognition. The most common cross-linking methods are based on reactive groups that interact with native or engineered cysteine residues. Nonetheless, high reactivity of most of such groups leads to preferential fixation of early-stage complexes or even non-selective cross-linking. We synthesised a set of DNA reagents carrying an acrylamide group attached to the C5 atom of a 2′-deoxyuridine moiety via various linkers and studied cross-linking with MutS as a model protein. MutS scans DNA for mismatches and damaged nucleobases and can form multiple non-specific complexes with DNA that may cause non-selective cross-linking. By varying the length of the linker between DNA and the acrylamide group and by changing the distance between the reactive nucleotide and a mismatch in the duplex, we showed that cross-linking occurs only if the distance between the acrylamide group and cysteine is optimal within the DNA–protein complex. Thus, acrylamide-modified DNA duplexes are excellent tools for studying DNA–protein interactions because of high selectivity of cysteine trapping. [ABSTRACT FROM AUTHOR]
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- 2022
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5. Involvement of E. coli 6S RNA in Oxidative Stress Response.
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Burenina, Olga Y., Elkina, Daria A., Ovcharenko, Anna, Bannikova, Valeria A., Schlüter, M. Amri C., Oretskaya, Tatiana S., Hartmann, Roland K., and Kubareva, Elena A.
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ESCHERICHIA coli , *OXIDATIVE stress , *BACTERIAL RNA , *RNA , *NON-coding RNA , *RNA polymerases - Abstract
6S RNA, a small non-coding RNA present in almost all bacteria, inhibits transcription via direct binding to RNA polymerase holoenzymes. The mechanism of 6S RNA action was investigated to a large extent in E. coli, however, lack of 6S RNA (ΔssrS) was demonstrated to be unfavorable but not essential for cell survival under various growth conditions. In the present study, we revealed, for the first time, a lethal phenotype of the ΔssrS strain in the presence of high concentrations of H2O2. This phenotype was rescued by complementation of the ssrS gene on a plasmid. We performed comparative qRT-PCR analyses on an enlarged set of mRNAs of genes associated with the oxidative stress response, allowing us to identify four genes known to be involved in this pathway (soxS, ahpC, sodA and tpx) that had decreased mRNA levels in the ΔssrS strain. Finally, we performed comparative proteomic analyses of the wild-type and ΔssrS strains, confirming that ΔssrS bacteria have reduced levels of the proteins AhpC and Tpx involved in H2O2 reduction. Our findings substantiate the crucial role of the riboregulator 6S RNA for bacterial coping with extreme stresses. [ABSTRACT FROM AUTHOR]
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- 2022
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6. Synthesis of 2′-hydrazine oligonucleotides and their efficient conjugation with aldehydes and 1,3-diketones
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Zatsepin, Timofei S., Gait, Michael J., Oretskaya, Tatiana S., and Stetsenko, Dmitry A.
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HYDRAZINES , *NUCLEOSIDES , *OLIGONUCLEOTIDES , *CHEMICAL reactions - Abstract
Abstract: Oligodeoxyribonucleotides that contain a novel nucleoside, 2′-O-(2-hydrazinoethyl)uridine, were synthesised by NaBH3CN reduction of hydrazones formed from 2′-O-(2-oxoethyl)oligonucleotides with FmocNHNH2, followed by concd aq NH3 deprotection. The 2′-hydrazine oligonucleotides obtained were then used to synthesise a number of conjugates with aldehydes via hydrazone formation and with1,3-diketones via pyrazole formation. The method was shown to be applicable for the preparation of oligonucleotide–peptide conjugates. [Copyright &y& Elsevier]
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- 2006
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7. Chemical synthesis of an artificially branched hairpin ribozyme variant with RNA cleavage activity
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Ivanov, Sergei A., Volkov, Eugene M., Oretskaya, Tatiana S., and Müller, Sabine
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RNA , *RIBOSE , *NUCLEOTIDES , *NUCLEIC acids - Abstract
Due to the development in the field of RNA synthesis over the past decade of years, preparation of RNA oligonucleotides longer than 50 nucleotides is possible today. In this report, we describe the chemical preparation of a branched RNA molecule with RNA cleavage activity consisting of 81 nucleotides. It is derived from the hairpin ribozyme, a small catalytic RNA occurring in nature. The hairpin ribozyme consists of two separately folded domains (loop A and loop B domain), which can be joined in a number of different ways without loss of activity. In the construct presented here, 2′-deoxy-N4-(6-hydroxyhexyl)-5-methylcytidine was introduced to connect the loop B domain with the loop A domain via an artificial branch. The synthesized branched RNA is able to catalyze the cleavage of a number of suitable substrates. Compared with the corresponding non-branched reverse-joined ribozyme it cleaves its substrates only 5-fold slower. Surprisingly, no ligation activity could be detected. [Copyright &y& Elsevier]
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- 2004
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8. 2′-Functionalized Nucleic Acids as Structural Tools in Molecular Biology.
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Zatsepin, Timofei S., Gait, Michael J., and Oretskaya, Tatiana S.
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OLIGONUCLEOTIDES , *BIOMOLECULES , *MOLECULES , *NUCLEIC acid hybridization , *FIRE assay , *MOLECULAR biology - Abstract
Modified oligonucleotides bearing 2′-reactive groups or 2′-conjugated molecules have found wide application as structural tools in molecular biology. Of principal interest has been the use of 2′-reactive oligonucleotides for cross-linking with biomolecules and of 2′-conjugated oligonucleotides in hybridization assays. In this review we compare a range of electrophilic, nucleophilic and photoreactive groups for cross-linking and conjugation studies. IUBMB Life, 56: 209-214, 2004 [ABSTRACT FROM AUTHOR]
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- 2004
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9. 1,2-Diol and Hydrazide Phosphoramidites for Solid-Phase Synthesis and Chemoselective Ligation of 2′-Modified Oligonucleotides.
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Zubin, Eugeny M., Stetsenko, Dmitry A., Oretskaya, Tatiana S., and Gait, Michael J.
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OLIGONUCLEOTIDES , *DNA , *ALDEHYDES , *PEPTIDES - Abstract
The preparation of two novel 2′-O-alkyl phosphoramidites bearing 1,2-diol and hydrazide functions for a chemoselective ligation is described. The former amidite was used to obtain 2′-modified oligodeoxyribonucleotides, which can be later oxidised by NaIO4 to generate 2′-aldehyde oligonucleotides. These were successfully conjugated to acceptor molecules. The latter amidite also showed good coupling yields, but the hydrazide function was demonstrated to be labile under basic deprotection conditions. [ABSTRACT FROM AUTHOR]
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- 2003
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10. A study on endonuclease BspD6I and its stimulus-responsive switching by modified oligonucleotides.
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Abrosimova, Liudmila A., Migur, Anzhela Yu., Kubareva, Elena A., Zatsepin, Timofei S., Gavshina, Aleksandra V., Yunusova, Alfiya K., Perevyazova, Tatiana A., Pingoud, Alfred, and Oretskaya, Tatiana S.
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ENDONUCLEASES , *OLIGONUCLEOTIDES , *DNA , *HETERODIMERS , *AZOBENZENE - Abstract
Nicking endonucleases (NEases) selectively cleave single DNA strands in double-stranded DNAs at a specific site. They are widely used in bioanalytical applications and in genome editing; however, the peculiarities of DNA–protein interactions for most of them are still poorly studied. Previously, it has been shown that the large subunit of heterodimeric restriction endonuclease BspD6I (Nt.BstD6I) acts as a NEase. Here we present a study of interaction of restriction endonuclease BspD6I with modified DNA containing single non-nucleotide insertion with an azobenzene moiety in the enzyme cleavage sites or in positions of sugar-phosphate backbone nearby. According to these data, we designed a number of effective stimulus-responsive oligonucleotide inhibitors bearing azobenzene or triethylene glycol residues. These modified oligonucleotides modulated the functional activity of Nt.BspD6I after cooling or heating. We were able to block the cleavage of T7 phage DNA by this enzyme in the presence of such inhibitors at 20–25°C, whereas the Nt.BspD6I ability to hydrolyze DNA was completely restored after heating to 45°C. The observed effects can serve as a basis for the development of a platform for regulation of NEase activity in vitro or in vivo by external signals. [ABSTRACT FROM AUTHOR]
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- 2018
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11. Analysis of the Cleavage Mechanism by Protein-Only RNase P Using Precursor tRNA Substrates with Modifications at the Cleavage Site.
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Walczyk, Dennis, Gößringer, Markus, Rossmanith, Walter, Zatsepin, Timofei S., Oretskaya, Tatiana S., and Hartmann, Roland K.
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TRANSFER RNA , *RIBONUCLEASES , *ENDONUCLEASES , *GENETIC transcription , *ARABIDOPSIS thaliana - Abstract
Ribonuclease P (RNase P) is the enzyme that endonucleolytically removes 5′-precursor sequences from tRNA transcripts in all domains of life. RNase P activities are either ribonucleoprotein (RNP) or protein-only RNase P (PRORP) enzymes, raising the question about the mechanistic strategies utilized by these architecturally different enzyme classes to catalyze the same type of reaction. Here, we analyzed the kinetics and cleavage-site selection by PRORP3 from Arabidopsis thaliana ( At PRORP3) using precursor tRNAs (pre-tRNAs) with individual modifications at the canonical cleavage site, with either R p- or S p-phosphorothioate, or 2′-deoxy, 2′-fluoro, 2′-amino, or 2′-O-methyl substitutions. We observed a small but robust rescue effect of S p-phosphorothioate-modified pre-tRNA in the presence of thiophilic Cd 2 + ions, consistent with metal-ion coordination to the (pro-) S p-oxygen during catalysis. S p-phosphorothioate, 2′-deoxy, 2′-amino, and 2′- O -methyl modification redirected the cleavage mainly to the next unmodified phosphodiester in the 5′-direction. Our findings are in line with the 2′-OH substituent at nucleotide − 1 being involved in an H-bonding acceptor function. In contrast to bacterial RNase P, At PRORP3 was found to be able to utilize the canonical and upstream cleavage site with similar efficiency (corresponding to reduced cleavage fidelity), and the two cleavage pathways appear less interdependent than in the bacterial RNA-based system. [ABSTRACT FROM AUTHOR]
- Published
- 2016
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12. Peculiarities of the interaction of the restriction endonuclease BspD6I with DNA containing its recognition site.
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Abrosimova, Liudmila A., Kubareva, Elena A., Migur, Anzhela Yu., Gavshina, Aleksandra V., Ryazanova, Aleksandra Yu., Norkin, Maxim V., Perevyazova, Tatiana A., Wende, Wolfgang, Hianik, Tibor, Zheleznaya, Liudmila A., and Oretskaya, Tatiana S.
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DNA restriction enzymes , *DNA replication , *DNA repair , *DNA-binding proteins , *GEL electrophoresis - Abstract
Background Nicking endonucleases are enzymes that recognize specific sites in double-stranded DNA and cleave only one strand at a predetermined position. These enzymes are involved in DNA replication and repair; they can also function as subunits of bacterial heterodimeric restriction endonucleases. One example of such a proteins is the restriction endonuclease BspD6I (R.BspD6I) from Bacillus species strain D6, which consists of the large subunit — nicking endonuclease BspD6I (Nt.BspD6I), and the small subunit (ss.BspD6I). Nt.BspD6I can function independently. Similar enzymes are now widely used in numerous biotechnological applications. The aim of this study was to investigate the fundamental properties of two subunits of R.BspD6I and their interdependence in the course of R.BspD6I activity. Methods The binding and hydrolysis of DNA duplexes by R.BspD6I are primary analyzed by gel electrophoresis. To elucidate the difference between Nt.BspD6I interaction with the substrate and product of hydrolysis, the thickness shear mode acoustic method is used. Results and conclusions The thermodynamic and kinetic parameters of the Nt.BspD6I interaction with DNA are determined. For the first time we demonstrated that Nt.BspD6I bends the DNA during complex formation. Nt.BspD6I is able to form complexes with the product nicked in the top strand and ss.BspD6I cleaves the bottom strand of the DNA consecutively. Furthermore, the influence of dA methylation in the R.BspD6I recognition site on ss.BspD6I activity is analyzed. General significance The obtained results provide evidence that Nt.BspD6I coordinates the activity of R.BspD6I by strictly coupling of the bottom strand cleavage by ss.BspD6I to the top strand cleavage. [ABSTRACT FROM AUTHOR]
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- 2016
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13. Is Thymidine Glycol Containing DNA a Substrate of E. coli DNA Mismatch Repair System?
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Perevozchikova, Svetlana A., Trikin, Roman M., Heinze, Roger J., Romanova, Elena A., Oretskaya, Tatiana S., Friedhoff, Peter, and Kubareva, Elena A.
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ESCHERICHIA coli , *THYMIDINE , *DNA repair , *DNA replication , *FLUORESCENCE anisotropy , *PLASMIDS - Abstract
The DNA mismatch repair (MMR) system plays a crucial role in the prevention of replication errors and in the correction of some oxidative damages of DNA bases. In the present work the most abundant oxidized pyrimidine lesion, 5,6-dihydro-5,6-dihydroxythymidine (thymidine glycol, Tg) was tested for being recognized and processed by the E. coli MMR system, namely complex of MutS, MutL and MutH proteins. In a partially reconstituted MMR system with MutS-MutL-MutH proteins, G/Tg and A/Tg containing plasmids failed to provoke the incision of DNA. Tg residue in the 30-mer DNA duplex destabilized double helix due to stacking disruption with neighboring bases. However, such local structural changes are not important for E. coli MMR system to recognize this lesion. A lack of repair of Tg containing DNA could be due to a failure of MutS (a first acting protein of MMR system) to interact with modified DNA in a proper way. It was shown that Tg in DNA does not affect on ATPase activity of MutS. On the other hand, MutS binding affinities to DNA containing Tg in G/Tg and A/Tg pairs are lower than to DNA with a G/T mismatch and similar to canonical DNA. Peculiarities of MutS interaction with DNA was monitored by Förster resonance energy transfer (FRET) and fluorescence anisotropy. Binding of MutS to Tg containing DNAs did not result in the formation of characteristic DNA kink. Nevertheless, MutS homodimer orientation on Tg-DNA is similar to that in the case of G/T-DNA. In contrast to G/T-DNA, neither G/Tg- nor A/Tg-DNA was able to stimulate ADP release from MutS better than canonical DNA. Thus, Tg residue in DNA is unlikely to be recognized or processed by the E. coli MMR system. Probably, the MutS transformation to active “sliding clamp” conformation on Tg-DNA is problematic. [ABSTRACT FROM AUTHOR]
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- 2014
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14. Thermo-switchable activity of the restriction endonuclease SsoII achieved by site-directed enzyme modification.
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Abrosimova, Liudmila A., Monakhova, Mayya V., Migur, Anzhela Yu., Wolfgang, Wende, Pingoud, Alfred, Kubareva, Elena A., and Oretskaya, Tatiana S.
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ENDONUCLEASES , *DEOXYRIBONUCLEOTIDES , *ENZYME kinetics , *DNA-protein interactions , *PROTEIN folding , *MOLECULAR biology - Abstract
In this work, the possibility of constructing a thermo-switchable enzyme according to the 'molecular gate' strategy is demonstrated. The approach is based on the covalent attachment of oligodeoxyribonucleotides to cysteine residues of an enzyme adjacent to its active center to form a temporal barrier for enzyme-substrate complex formation. The activity of the modified enzyme that had been studied here-the restriction endonuclease SsoII (R.SsoII)-was diminished by a factor of 180 at 25 °С that almost abolished the enzymatic activity when compared with the unmodified enzyme. However, heating of the modified enzyme to 45 °С resulted in a 30-fold increase of activity. The activity of unmodified R.SsoII also increased on heating from 25 to 45 °; however, the difference did not exceed a factor of 3-4. The changes in enzymatic activity observed were shown to be reversible for both the unmodified and the modified R.SsoII. Variation of the length and the sequence of the attached oligodeoxyribonucleotides might allow greater modulation of the activity of DNA-protein conjugates. © 2013 IUBMB Life, 65(12):1012-1016, 2013 [ABSTRACT FROM AUTHOR]
- Published
- 2013
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15. Clustered DNA Lesions Containing 5-Formyluracil and AP Site: Repair via the BER System.
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Belousova, Ekaterina A., Vasil'eva, Inna A., Moor, Nina A., Zatsepin, Timofey S., Oretskaya, Tatiana S., and Lavrik, Olga I.
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DNA repair , *OXIDIZING agents , *DNA damage , *APURINIC acid , *ENDONUCLEASES , *DNA synthesis , *DNA polymerases - Abstract
Lesions in the DNA arise under ionizing irradiation conditions or various chemical oxidants as a single damage or as part of a multiply damaged site within 1–2 helical turns (clustered lesion). Here, we explored the repair opportunity of the apurinic/apyrimidinic site (AP site) composed of the clustered lesion with 5-formyluracil (5-foU) by the base excision repair (BER) proteins. We found, that if the AP site is shifted relative to the 5-foU of the opposite strand, it could be repaired primarily via the short-patch BER pathway. In this case, the cleavage efficiency of the AP site-containing DNA strand catalyzed by human apurinic/apyrimidinic endonuclease 1 (hAPE1) decreased under AP site excursion to the 3'-side relative to the lesion in the other DNA strand. DNA synthesis catalyzed by DNA polymerase lambda was more accurate in comparison to the one catalyzed by DNA polymerase beta. If the AP site was located exactly opposite 5-foU it was expected to switch the repair to the long-patch BER pathway. In this situation, human processivity factor hPCNA stimulates the process. [ABSTRACT FROM AUTHOR]
- Published
- 2013
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16. Thymidine glycol: the effect on DNA molecular structure and enzymatic processing
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Dolinnaya, Nina G., Kubareva, Elena A., Romanova, Elena A., Trikin, Roman M., and Oretskaya, Tatiana S.
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THYMINE glycol , *DNA structure , *DNA damage , *IONIZING radiation , *DIASTEREOISOMERS , *DNA polymerases , *DNA repair - Abstract
Abstract: Thymine glycol (Tg) in DNA is a biologically active oxidative damage caused by ionizing radiation or oxidative stress. Due to chirality of C5 and C6 atoms, Tg exists as a mixture of two pairs of cis and trans diastereomers: 5R cis–trans pair (5R,6S; 5R,6R) and 5S cis–trans pair (5S,6R; 5S,6S). Of all the modified pyrimidine lesions that have been studied to date, only thymine glycol represents a strong block to high-fidelity DNA polymerases in vitro and is lethal in vivo. Here we describe the preparation of thymine glycol-containing oligonucleotides and the influence of the oxidized residue on the structure of DNA in different sequence contexts, thymine glycol being paired with either adenine or guanine. The effect of thymine glycol on biochemical processing of DNA, such as biosynthesis, transcription and repair in vitro and in vivo, is also reviewed. Special attention is paid to stereochemistry and 5R cis–trans epimerization of Tg, and their relation to the structure of DNA double helix and enzyme-mediated DNA processing. Described here are the comparative structure and properties of other forms of pyrimidine base oxidation, as well as the role of Tg in tandem lesions. [Copyright &y& Elsevier]
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- 2013
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17. DNA Poiymerases β and λ Bypass Thymine Glycol in Gapped DNA Structures.
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Belousova, Ekaterina A., Maga, Giovanni, Yang Fan, Kubareva, Elena A., Romanova, Elena A., Lebedeva, Natalia A., Oretskaya, Tatiana S., and Lavrik, Olga I.
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DNA polymerases , *THYMINE , *GLYCOLS , *DNA synthesis , *MAGNESIUM , *MANGANESE , *PROTEINS , *DNA damage - Abstract
Here we investigated the ability of the human X-family DNA polymerases β and λ to bypass thymine glycol (Tg) in gapped DNA substrates with the damage located in a defined position of the template strand. Maximum velocities and the Michaelis constant values were determined to study DNA synthesis in the presence of either Mg2+ or Mn2+. Additionally, the influence of hRPA (human replication protein A) and hPCNA (human proliferating cell nuclear antigen) on TLS (translesion synthesis) activity of DNA polymerases β and λ was examined. The results show that (i) DNA polymerase λ is able to catalyze DNA synthesis across Tg, (ii) the ability of DNA polymerase λ to elongate from a base paired to a Tg lesion is influenced by the size of the DNA gap, (iii)hPCNA increases the fidelity of Tg bypass and does not influence normal DNA synthesis catalyzed by DNA polymerase λ. (iv) DNA polymerase β catalyzes the incorporation of all four dNTPs opposite Tg, and (v) hPCNA as well as hRPA has no specific effect on TLS in comparison with the normal DNA synthesis catalyzed by DNA polymerase β. These results considerably extend our knowledge concerning the ability of specialized DNA polymerases to cope with a very common DNA lesion such as Tg. [ABSTRACT FROM AUTHOR]
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- 2010
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18. Kinetic Analysis of the Interaction of Nicking Endonuclease BspD6I with DNA.
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Abrosimova, Liudmila A., Kuznetsov, Nikita A., Astafurova, Natalia A., Samsonova, Anastasiia R., Karpov, Andrey S., Perevyazova, Tatiana A., Oretskaya, Tatiana S., Fedorova, Olga S., and Kubareva, Elena A.
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DEOXYRIBOZYMES , *DNA , *ENDONUCLEASES , *NUCLEIC acids , *GENOME editing , *GENETIC engineering - Abstract
Nicking endonucleases (NEs) are enzymes that incise only one strand of the duplex to produce a DNA molecule that is 'nicked' rather than cleaved in two. Since these precision tools are used in genetic engineering and genome editing, information about their mechanism of action at all stages of DNA recognition and phosphodiester bond hydrolysis is essential. For the first time, fast kinetics of the Nt.BspD6I interaction with DNA were studied by the stopped-flow technique, and changes of optical characteristics were registered for the enzyme or DNA molecules. The role of divalent metal cations was estimated at all steps of Nt.BspD6I–DNA complex formation. It was demonstrated that divalent metal ions are not required for the formation of a non-specific complex of the protein with DNA. Nt.BspD6I bound five-fold more efficiently to its recognition site in DNA than to a random DNA. DNA bending was confirmed during the specific binding of Nt.BspD6I to a substrate. The optimal size of Nt.BspD6I's binding site in DNA as determined in this work should be taken into account in methods of detection of nucleic acid sequences and/or even various base modifications by means of NEs. [ABSTRACT FROM AUTHOR]
- Published
- 2021
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19. Oligonucleotides containing 2′-O-[2-(2,3-dihydroxypropyl)amino-2-oxoethyl]uridine as suitable precursors of 2′-aldehyde oligonucleotides for chemoselective ligation
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Zubin, Eugeny M., Stetsenko, Dmitry A., Zatsepin, Timofei S., Gait, Michael J., and Oretskaya, Tatiana S.
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NUCLEOTIDES , *OLIGONUCLEOTIDES , *ORGANIC compounds , *CHEMICAL reactions - Abstract
Abstract: 2′-O-[2-(2,3-Diacetoxypropyl)amino-2-oxoethyl]uridine 3′-phosphoramidite was prepared and used in solid-phase synthesis to obtain oligonucleotides containing a 1,2-diol group, which may then be converted into a 2′-aldehyde group. The oligonucleotides were conjugated efficiently to various molecules by chemoselective ligation that involves an addition–elimination reaction between the 2′-aldehyde group and a suitable nucleophile, such as a hydrazine, a O-alkylhydroxylamine or an 1,2-aminothiol. The method was applied successfully to the conjugation of peptides to oligonucleotides at the 2′-position. [Copyright &y& Elsevier]
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- 2005
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20. Synthesis of DNA conjugates by solid-phase fragment condensation via aldehyde–nucleophile coupling
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Zatsepin, Timofei S., Stetsenko, Dmitry A., Gait, Michael J., and Oretskaya, Tatiana S.
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OLIGONUCLEOTIDES , *ORGANIC compounds , *VITAMIN B complex , *PROTEINS - Abstract
Abstract: Oligodeoxyribonucleotides were synthesized that contain a novel nucleoside, 2′-O-(2,3-dihydroxypropyl)cytidine. Its 2′-diol group was blocked by an allyloxycarbonyl protecting group. Selective deprotection of diol group(s) of the support-immobilized blocked oligodeoxyribonucleotide by Pd(0) followed by periodate oxidation resulted in generation of the 2′-aldehyde group(s) on solid-phase. The modified oligonucleotides were used to prepare a number of conjugates with acridine, biotin and N-modified laminin peptides by oxime, hydrazone and hydrazine formation. The method may be applicable to the synthesis of oligonucleotide–peptide conjugates. [Copyright &y& Elsevier]
- Published
- 2005
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21. Efficient conjugation and preferential DNA binding of oligonucleotides containing 2′-O-(2-oxoethyl)arabinouridine
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Zatsepin, Timofei S., Ivanova, Yulia M., Stetsenko, Dmitry A., Gait, Michael J., and Oretskaya, Tatiana S.
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- 2004
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22. Detection of DNA hybridization on a liposome surface using ultrasound velocimetry and turbidimetry methods
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Hianik, Tibor, Rybar, Peter, Andreev, Sergej Yu., Oretskaya, Tatiana S., and Vadgama, Pankaj
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DNA , *NUCLEIC acid hybridization , *LIPOSOMES , *CYTOPLASM - Abstract
19-mer oligonucleotides with oleylamine tethered at 3′ and 5′ terminal, respectively, were incorporated into unilamellar liposomes of dioleoylphosphatidylcholine (DOPC). Addition of complementary nucleotide resulted in hybridization with oligonucleotides located on different liposomes and caused liposome aggregation. Significant changes of sound velocimetry and turbidity were readily observed at 10 nM concentration of the complementary chain. [Copyright &y& Elsevier]
- Published
- 2004
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23. Synthesis of oligonucleotide 2′-conjugates via amide bond formation in solution
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Kachalova, Anna V., Stetsenko, Dmitry A., Gait, Michael J., and Oretskaya, Tatiana S.
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OLIGONUCLEOTIDES , *SODIUM chlorate , *ALDEHYDES , *AMINO acids - Abstract
An efficient method for synthesis of 2′-O-carboxymethyl oligonucleotides is described. Fully deprotected oligonucleotides containing a carboxymethyl group at the 2′-position of sugar residue were obtained by a two-step procedure by periodate cleavage of an oligonucleotide containing 1,2-diol group followed by oxidation of the 2′-aldehyde resulted with sodium chlorite. 2′-O-Carboxymethyl oligonucleotides prepared were efficiently coupled in aqueous solution in the presence of a water-soluble carbodiimide to a number of amino acid derivatives or short peptides to afford novel 2′-conjugates of high purity in good yield. The method is thus shown to be suitable in principle for preparation of oligonucleotide–peptide conjugates containing an amide linkage between the 2′-carboxy group of a modified oligonucleotide and the amino terminus of a peptide. [Copyright &y& Elsevier]
- Published
- 2004
- Full Text
- View/download PDF
24. Specific conjugation of DNA binding proteins to DNA templates through thiol–disulfide exchange
- Author
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Metelev, Valeri G., Kubareva, Elena A., Vorob’eva, Olga V., Romanenkov, Andrey S., and Oretskaya, Tatiana S.
- Subjects
- *
CARRIER proteins , *CYSTEINE proteinases , *DNA - Abstract
The double-stranded oligodeoxyribonucleotides with single internucleotide disulfide linkages were successfully used for covalent trapping of cysteine containing protein. In particular, an efficient conjugation of DNA methyltransferase SsoII to sequence-specific decoys was demonstrated. The obtained results assume that synthetic oligodeoxyribonucleotides bearing a new trapping site can be used as new tools to study and manipulate biological systems. [Copyright &y& Elsevier]
- Published
- 2003
- Full Text
- View/download PDF
25. Responses of DNA Mismatch Repair Proteins to a Stable G-Quadruplex Embedded into a DNA Duplex Structure.
- Author
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Pavlova, Anzhela V., Monakhova, Mayya V., Ogloblina, Anna M., Andreeva, Natalia A., Laptev, Gennady Yu., Polshakov, Vladimir I., Gromova, Elizaveta S., Zvereva, Maria I., Yakubovskaya, Marianna G., Oretskaya, Tatiana S., Kubareva, Elena A., and Dolinnaya, Nina G.
- Subjects
- *
DNA mismatch repair , *DNA structure , *FLUORESCENT probes , *RHODOBACTER sphaeroides , *PROTEINS , *CIRCULAR dichroism - Abstract
DNA mismatch repair (MMR) plays a crucial role in the maintenance of genomic stability. The main MMR protein, MutS, was recently shown to recognize the G-quadruplex (G4) DNA structures, which, along with regulatory functions, have a negative impact on genome integrity. Here, we studied the effect of G4 on the DNA-binding activity of MutS from Rhodobacter sphaeroides (methyl-independent MMR) in comparison with MutS from Escherichia coli (methyl-directed MMR) and evaluated the influence of a G4 on the functioning of other proteins involved in the initial steps of MMR. For this purpose, a new DNA construct was designed containing a biologically relevant intramolecular stable G4 structure flanked by double-stranded regions with the set of DNA sites required for MMR initiation. The secondary structure of this model was examined using NMR spectroscopy, chemical probing, fluorescent indicators, circular dichroism, and UV spectroscopy. The results unambiguously showed that the d(GGGT)4 motif, when embedded in a double-stranded context, adopts a G4 structure of a parallel topology. Despite strong binding affinities of MutS and MutL for a G4, the latter is not recognized by E. coli MMR as a signal for repair, but does not prevent MMR processing when a G4 and G/T mismatch are in close proximity. [ABSTRACT FROM AUTHOR]
- Published
- 2020
- Full Text
- View/download PDF
26. Kinetic Basis of the Bifunctionality of SsoII DNA Methyltransferase.
- Author
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Timofeyeva, Nadezhda A., Ryazanova, Alexandra Yu., Norkin, Maxim V., Oretskaya, Tatiana S., Fedorova, Olga S., Kubareva, Elena A., and Iwahara, Junji
- Subjects
- *
METHYLTRANSFERASES , *TRANSMETHYLATION , *DNA , *METHYLATION , *ANTIVIRAL agents - Abstract
Type II restriction–modification (RM) systems are the most widespread bacterial antiviral defence mechanisms. DNA methyltransferase SsoII (M.SsoII) from a Type II RM system SsoII regulates transcription in its own RM system in addition to the methylation function. DNA with a so-called regulatory site inhibits the M.SsoII methylation activity. Using circular permutation assay, we show that M.SsoII monomer induces DNA bending of 31° at the methylation site and 46° at the regulatory site. In the M.SsoII dimer bound to the regulatory site, both protein subunits make equal contributions to the DNA bending, and both angles are in the same plane. Fluorescence of TAMRA, 2-aminopurine, and Trp was used to monitor conformational dynamics of DNA and M.SsoII under pre-steady-state conditions by stopped-flow technique. Kinetic data indicate that M.SsoII prefers the regulatory site to the methylation site at the step of initial protein–DNA complex formation. Nevertheless, in the presence of
S -adenosyl-l-methionine, the induced fit is accelerated in the M.SsoII complex with the methylation site, ensuring efficient formation of the catalytically competent complex. The presence ofS -adenosyl-l-methionine and large amount of the methylation sites promote efficient DNA methylation by M.SsoII despite the inhibitory effect of the regulatory site. [ABSTRACT FROM AUTHOR]- Published
- 2018
- Full Text
- View/download PDF
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