Publications by authors named "alexander S Tatikolov"

Bilirubin, a yellow bile pigment, plays an important role in the body, being a potent antioxidant and having anti-inflammatory, immunomodulatory, cytoprotective, and neuroprotective functions. This makes bilirubin promising as a therapeutic and diagnostic agent in biomedicine. However, excess bilirubin is toxic and should be removed from the body.

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Trimethine cyanine dyes are widely used as probes for the detection, study and quantification of biomolecules. In particular, cationic trimethine cyanines noncovalently interact with DNA with growing fluorescence. However, their use is often limited by the tendency to self-association - to the formation of aggregates.

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In search of new probes for biomolecules, the spectral fluorescent study of four monomethine cyanine dyes (MCD), both unsymmetrical and symmetrical, has been carried out in different organic solvents, in aqueous buffer solutions, and in the presence of DNA and HSA. The complexation of MCD with biomacromolecules leads to a steep growth of the fluorescence intensity. Complexes of MCD with dsDNA and HSA of various types were modeled in silico by molecular docking.

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The use of conventional contrast media for diagnostic purposes (in particular, Gd-containing and iodinated agents) causes a large number of complications, the most common of which is contrast-induced nephropathy. It has been shown that after exposure to contrast agents, oxidative stress often occurs in patients, especially in people suffering from various diseases. Antioxidants in the human body can diminish the pathological consequences of the use of contrast media by suppressing oxidative stress.

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Article Synopsis
  • Cyanine dyes are important fluorescent probes in biophysics and medical biochemistry, particularly focusing on trimethine cyanines, which are studied for their interactions with biomolecules.
  • The review explores how trimethine cyanine dyes exhibit changes in their spectral and photochemical properties upon interacting with biomolecules like DNA and proteins, often resulting in increased fluorescence.
  • The text highlights the potential practical applications of these dyes in research and discusses future insights into developing new dye probes for biomolecular studies.
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Article Synopsis
  • The study investigates how two specific thiacarbocyanine dyes interact with double-stranded (dsDNA) and single-stranded (ssDNA) in water, using spectral and fluorescent methods.
  • Complexation with DNA causes both the aggregation of the dyes and the creation of highly fluorescent complexes, indicating that the dyes can intercalate between base pairs and bind in the grooves of the DNA structure.
  • The research also finds that the presence of these dyes increases the stability of dsDNA, similar to a well-known DNA intercalator, and provides insights into their potential application as DNA probes while exploring their photochemical behavior when bound to ssDNA.
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Spectral-fluorescent and photochemical properties (photoisomerization and generation of the triplet state) of meso-substituted cationic carbocyanine dyes, 3,3'-di-(β-hydroxyethyl)-5,5'-dimethoxy-9-ethylthiacarbocyanine iodide (K1) and 3,3'-di-(β-hydroxyethyl)-9-methylthiacarbocyanine iodide (K2), have been studied in solutions and in the presence of DNA. In solutions, on passing from acetonitrile to dioxane, a growth of fluorescence of the dyes is observed due to a shift of the equilibrium of cis/trans isomers toward the fluorescent trans-isomer. Upon flash photolysis of dye solutions in dioxane, the formation and subsequent decay of the cis-photoisomers of the dyes are observed.

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Spectral-fluorescent properties of polymethine dye probes anionic 3,3'-di(sulfopropyl)-4,5,4',5'-dibenzo-9-ethylthiacarbocyanine-betaine (DEC) and cationic 3,3',9-trimethylthiacarbocyanine iodide (Cyan 2) in the presence of biological surfactants, bile salts sodium cholate (NaC), sodium deoxycholate (NaDC) and sodium taurocholate (NaTC), as well as sodium dodecyl sulfate (SDS), have been studied in a wide range of surfactant concentrations. When a surfactant is introduced into a solution of DEC, changes of the spectral-fluorescent properties are observed due to decomposition of dye dimers into cis-monomers and cis-trans conversion of the resulting monomers. In the presence of SDS, both processes occur in parallel, caused by noncovalent interaction of dye monomers with micelles, and mainly occur near the critical micelle concentration (CMC).

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Article Synopsis
  • The study investigates the spectral-fluorescent and photochemical properties of specific thiacarbocyanine dyes and their interactions with DNA.
  • The dyes form noncovalent complexes with DNA, changing their absorption spectra and increasing fluorescence intensity, while existing as trans-isomers in various environments.
  • Flash photolysis technique reveals that the dyes undergo complex photochemical processes, with the formation of triplet states influencing their behavior in DNA complexes.
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The presence of carotenoids in the vitreous body, retina, lens, retinal pigment epithelium together with choroid (hereinafter RPE), and ciliary body and iris together with choroidal stroma (hereinafter CBI) was studied throughout the second trimester of prenatal development of the human eye. It has been found that the vitreous body, retina, and RPE contain lutein and its oxidized forms. Zeaxanthin was not found in the tissues studied.

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A novel biphotochromic compound (BPC) with two photochromic fragments, namely spironaphthopyran and hydroxyazomethine, was synthesized and studied by nanosecond laser flash photolysis using the excitation wavelengths of 337, 430, 470 and 500 nm in methanol and toluene. The photoexcitation of BPC results in the formation of at least two colored transients. The first one is the merocyanine form B (the maximum in the absorption spectrum is near 600 nm and the lifetime is 0.

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The electronic structure, spectra and linear and second-order polarizabilities of two symmetric ketocyanines, which are prototypic examples of D-A-D chromophores, have been investigated with two different toolsets: (i) the so-called 'essential-state model', here comprising three states, the ground and two lowest excited (1)ππ* states, has been adapted for these non-centrosymmetric, yet symmetric compounds to determine their permanent electric dipole moments, polarizabilities and first hyperpolarizabilities making use of experimental transition energies and moments; (ii) extensive TDDFT calculations have provided ground-state conformational results consistent with NMR-derived structural information, energies and dipole moments of up to 20 lowest-lying electronic states as well as, within the sum-over-states (SOS) scheme, the most relevant components of the polarizabilities and first hyperpolarizabilities. The two levels of description form consistent pictures of the ketocyanine excited states that provide the most relevant contributions to hyperpolarizabilities: extension of the SOS set beyond the three states of the basic model left unchanged (within ∼10%) the calculated vector component of the second-order polarizability tensor along the direction of the ground-state dipole moment (β(y)). Both approaches indicate that these D-A-D compounds, in spite of their quasi-linear structure, reminiscent of that of centrosymmetric quadrupolar chromophores, feature significant second-order molecular polarizabilities.

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This study aimed to analyze the aqueous humor (AH) and the vitreous body (VB) of the eye of the adult frog Rana temporaria L. as a representative species of amphibians, which lead a semi-terrestrial life. The presence of collagen, albumin, uric acid and electron donors was shown in both media; however, there are slight differences in their concentrations.

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The aim of this work was to develop a quick method for analysis of macromolecules of the extracellular matrix. Of great interest are soluble components of the extracellular matrix, in particular, carrier proteins, whose variation dynamics can characterize the studied tissue in its development, adult stage, and aging. We suggest the method of analysis of the extracellular matrix to reveal the presence of albumin and collagen by using an anionic cyanine dye as a spectral and fluorescence probe.

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Electronic excitation energy transfer (EET) between molecules of polymethine dyes bound to human serum albumin (HSA) has been established and studied by absorption and fluorescence spectroscopy as well as by fluorescence decay measurements. In this system, excitation of the donor dye molecule leads to fluorescence of the acceptor dye molecule, both bound to HSA, with donor fluorescence quenching by the acceptor. The short distance between the donor and the acceptor (25-28 A) revealed from the Forster model of EET as well as some spectroscopic data show that both molecules are probably located in the same binding domain of HSA.

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Non-covalent interactions between polymethine dyes of various types (cationic and anionic thiacarbocyanines as well as anionic oxonols and tetracyanopolymethines) and human serum albumin (HSA) were studied by means of absorption, fluorescence and circular dichroism (CD) spectroscopies. Complexation with the protein leads to a red shift of the dye absorption spectra and, in most cases, to a growth of the fluorescence quantum yield (Phif; for oxonols this growth is very small). The binding constants (K) obtained from changing the absorption spectra and Phif vary from 10(4) to (5-6) x 10(7) M(-1).

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The photophysical and photochemical properties of the negatively charged hydrophilic cyanine dyes 1-3 were studied in isooctane/sodium bis(2-ethylhexyl) sulfosuccinate (AOT)/water and cyclohexane-hexanol/Triton X-100 (TX100)/water reverse micelles and in aqueous solutions in the presence of surfactants. In spite of the opposite total charges, 2 and its structural analog, cationic 3,3'-diethylthiacarbocyanine (DTC), show similar photophysical and photochemical behaviour in AOT reverse micelles. However, in normal micelles their photophysical properties are quite different: 2 exhibits unusual behaviour [a sharp increase in the fluorescence quantum yield (phif) in the presence of both cationic and anionic micelles, but very small changes with neutral TX100], whereas the behaviour of DTC is normal.

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Synopsis of recent research by authors named "alexander S Tatikolov"

  • - Alexander S. Tatikolov's recent research primarily focuses on the development and analysis of photonic dyes, particularly cyanine dyes, and their interactions with biomolecules like DNA and proteins, with implications for their use as fluorescent probes in biochemistry and biophysics.
  • - His studies explore the spectral-fluorescent properties and behavior of both trimethine and monomethine cyanine dyes in various solutions and conditions, highlighting their complexation with DNA, which significantly enhances their fluorescence and potential applications in molecular diagnostics.
  • - Tatikolov also investigates the role of antioxidants in mitigating the adverse effects of contrast media used in medical imaging, emphasizing the oxidative stress caused by these agents and the importance of antioxidant defense mechanisms in preventing contrast-induced nephropathy.