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Visible Light-Induced Templated Metathesis of Peptide–Nucleic Acid Conjugates with a Diselenide Bridge.
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- Biomolecules (2218-273X), 2023, v. 13, n. 11, p. 1676, doi. 10.3390/biom13111676
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Peptide Stapling with Boronate Esters‐ A Reversible Folding of (Artificial) Peptide Chain to α‐Helix.
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- Chemistry - A European Journal, 2023, v. 29, n. 40, p. 1, doi. 10.1002/chem.202301370
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Selenium in Peptide Chemistry.
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- Molecules, 2023, v. 28, n. 7, p. 3198, doi. 10.3390/molecules28073198
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HPLC–free method of synthesis of isotopically labeled deoxyfructosylated peptides.
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- Analytical & Bioanalytical Chemistry, 2022, v. 414, n. 13, p. 3803, doi. 10.1007/s00216-022-04022-6
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Analysis of Fragmentation Pathways of Peptide Modified with Quaternary Ammonium and Phosphonium Group as Ionization Enhancers.
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- Molecules, 2021, v. 26, n. 22, p. 6964, doi. 10.3390/molecules26226964
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Isolation, characterization, anti-MRSA evaluation, and in-silico multi-target anti-microbial validations of actinomycin X2 and actinomycin D produced by novel Streptomyces smyrnaeus UKAQ_23.
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- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-93285-7
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Synthesis and Mass Spectrometry Analysis of Mimosine-Containing Peptides.
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- International Journal of Peptide Research & Therapeutics, 2021, v. 27, n. 1, p. 379, doi. 10.1007/s10989-020-10092-w
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Attempting to synthesize lasso peptides using high pressure.
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- PLoS ONE, 2020, v. 15, n. 6, p. 1, doi. 10.1371/journal.pone.0234901
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Detection of Podocin in Human Urine Sediment Samples by Charge Derivatization and LC-MS-MRM Method.
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- International Journal of Molecular Sciences, 2020, v. 21, n. 9, p. 3225, doi. 10.3390/ijms21093225
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An Optimised Di-Boronate-ChemMatrix Affinity Chromatography to Trap Deoxyfructosylated Peptides as Biomarkers of Glycation.
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- Molecules, 2020, v. 25, n. 3, p. 755, doi. 10.3390/molecules25030755
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- Article
Light‐Driven Diselenide Metathesis in Peptides.
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- ChemistryOpen, 2019, v. 8, n. 9, p. 1199, doi. 10.1002/open.201900224
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Trends in the Design of New Isobaric Labeling Reagents for Quantitative Proteomics.
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- Molecules, 2019, v. 24, n. 4, p. 701, doi. 10.3390/molecules24040701
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Self‐Synthesizing Models of Helical Proteins Based on Aromatic Disulfide Chemistry.
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- Chemistry - A European Journal, 2018, v. 24, n. 49, p. 12869, doi. 10.1002/chem.201800187
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Peptides Labeled with Pyridinium Salts for Sensitive Detection and Sequencing by Electrospray Tandem Mass Spectrometry.
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- Scientific Reports, 2016, p. 37720, doi. 10.1038/srep37720
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- Article
The influence of glycation on a high pressure denaturation of ubiquitin.
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- Bioscience Reports, 2016, v. 36, n. 5, p. 1, doi. 10.1042/BSR20160233
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Cyclodimerization of immunosuppressive fragment of HLA-DR molecule. Design, synthesis and ESI-MS/MS analysis.
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- Journal of Peptide Science, 2016, v. 22, n. 8, p. 525, doi. 10.1002/psc.2898
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Phenolic Constituents from Alchornea castaneifolia.
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- Records of Natural Products, 2016, v. 10, n. 1, p. 32
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Synthesis and mass spectrometry analysis of quaternary cryptando-peptidic conjugates.
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- Journal of Peptide Science, 2015, v. 21, n. 12, p. 879, doi. 10.1002/psc.2830
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Convenient preparation of deuterium-labeled analogs of peptides containing N-substituted glycines for a stable isotope dilution LC-MS quantitative analysis.
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- Journal of Peptide Science, 2015, v. 21, n. 11, p. 819, doi. 10.1002/psc.2823
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Facile synthesis of deuterium-labeled denatonium cation and its application in the quantitative analysis of Bitrex by liquid chromatography-mass spectrometry.
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- Analytical & Bioanalytical Chemistry, 2015, v. 407, n. 21, p. 6557, doi. 10.1007/s00216-015-8815-y
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Site-selective solid phase synthesis of carbonylated peptides.
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- Amino Acids, 2015, v. 47, n. 7, p. 1353, doi. 10.1007/s00726-015-1967-4
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N-terminal guanidinylation of the cyclic 1,4-ureido-deltorphin analogues: the synthesis, receptor binding studies, and resistance to proteolytic digestion.
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- Journal of Peptide Science, 2015, v. 21, n. 6, p. 467, doi. 10.1002/psc.2762
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Comparison of modification sites in glycated crystallin in vitro and in vivo.
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- Analytical & Bioanalytical Chemistry, 2015, v. 407, n. 9, p. 2557, doi. 10.1007/s00216-015-8487-7
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Hydrogen-deuterium exchange in imidazole as a tool for studying histidine phosphorylation.
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- Analytical & Bioanalytical Chemistry, 2014, v. 406, n. 30, p. 8013, doi. 10.1007/s00216-014-8218-5
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Determination of Ursolic and Oleanolic Acid in Sambuci Fructus.
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- Chemistry & Biodiversity, 2014, v. 11, n. 12, p. 1939, doi. 10.1002/cbdv.201400118
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The mass spectrometric study on aminohydroxamic acids-based metallacrowns.
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- Journal of Mass Spectrometry, 2014, v. 49, n. 11, p. 1156, doi. 10.1002/jms.3438
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Microwave-assisted <sup>18</sup>O labeling of Fmoc-protected amino acids.
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- Journal of Peptide Science, 2014, v. 20, n. 11, p. 896, doi. 10.1002/psc.2682
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- Article
Hydrogen-deuterium exchange of α-carbon protons and fragmentation pathways in N-methylated glycine and alanine-containing peptides derivatized by quaternary ammonium salts.
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- Journal of Mass Spectrometry, 2014, v. 49, n. 6, p. 529, doi. 10.1002/jms.3371
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The unusual hydrogen-deuterium exchange of α-carbon protons in N-substituted glycine-containing peptides.
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- Journal of Mass Spectrometry, 2014, v. 49, n. 1, p. 43, doi. 10.1002/jms.3318
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New method of peptide cleavage based on Edman degradation.
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- Molecular Diversity, 2013, v. 17, n. 3, p. 605, doi. 10.1007/s11030-013-9453-y
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One-pot efficient synthesis of N-urethane-protected β- and γ-amino acids.
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- Amino Acids, 2013, v. 44, n. 3, p. 1085, doi. 10.1007/s00726-012-1443-3
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Solid phase synthesis of peptide hydroxamic acids on poly(ethylene glycol)-based support.
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- Journal of Peptide Science, 2013, v. 19, n. 1, p. 9, doi. 10.1002/psc.2466
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Hydrogen scrambling in non-covalent complexes of peptides.
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- Rapid Communications in Mass Spectrometry: RCM, 2012, v. 26, n. 23, p. 2739, doi. 10.1002/rcm.6396
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- Article
Interaction of serum amyloid A with human cystatin C-identification of binding sites.
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- Journal of Molecular Recognition, 2012, v. 25, n. 10, p. 513, doi. 10.1002/jmr.2220
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Pressure as a denaturing agent in studies of single-point mutants of an amyloidogenic protein human cystatin c.
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- Proteins, 2012, v. 80, n. 10, p. 2417, doi. 10.1002/prot.24126
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Sensitive electrospray mass spectrometry analysis of one-bead-one-compound peptide libraries labeled by quaternary ammonium salts.
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- Molecular Diversity, 2012, v. 16, n. 3, p. 613, doi. 10.1007/s11030-012-9377-y
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Dimeric analogs of immunosuppressive decapeptide fragment of ubiquitin.
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- Journal of Peptide Science, 2012, v. 18, n. 7, p. 456, doi. 10.1002/psc.2416
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Derivatization of peptides as quaternary ammonium salts for sensitive detection by ESI-MS.
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- Journal of Peptide Science, 2011, v. 17, n. 6, p. 445, doi. 10.1002/psc.1342
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The efficient synthesis of isotopically labeled peptide-derived Amadori products and their characterization.
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- Amino Acids, 2011, v. 40, n. 3, p. 923, doi. 10.1007/s00726-010-0714-0
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Electron capture dissociation mass spectrometric analysis of lysine-phosphorylated peptides.
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- Bioscience Reports, 2010, v. 30, n. 6, p. 433, doi. 10.1042/BSR20090167
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Capric Acid Secreted by S. boulardii Inhibits C. albicans Filamentous Growth, Adhesion and Biofilm Formation.
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- PLoS ONE, 2010, v. 5, n. 8, p. 1, doi. 10.1371/journal.pone.0012050
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Inhibitory activity of double-sequence analogues of trypsin inhibitor SFTI-1 from sunflower seeds: an example of peptide splicing.
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- FEBS Journal, 2010, v. 277, n. 10, p. 2351, doi. 10.1111/j.1742-4658.2010.07650.x
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- Article
Ubiquitin fragments: their known biological activities and putative roles.
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- Biomolecular Concepts, 2010, v. 1, n. 1, p. 67, doi. 10.1515/BMC.2010.002
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Electrospray ionization mass spectrometry as a method for studying the high-pressure denaturation of proteins.
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- Bioscience Reports, 2010, v. 30, n. 2, p. 91, doi. 10.1042/BSR20090015
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Methods of the site-selective solid phase synthesis of peptide-derived Amadori products.
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- Amino Acids, 2010, v. 38, n. 3, p. 881, doi. 10.1007/s00726-009-0294-z
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Microwave-assisted TFA cleavage of peptides from Merrifield resin.
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- Journal of Peptide Science, 2010, v. 16, n. 1, p. 31, doi. 10.1002/psc.1191
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- Article
Electrospray ionization mass spectrometric analysis of complexes between peptide-derived Amadori products and borate ions.
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- Rapid Communications in Mass Spectrometry: RCM, 2009, v. 23, n. 24, p. 4038, doi. 10.1002/rcm.4347
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Sequencing of peptide-derived Amadori products by the electron capture dissociation method.
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- Journal of Mass Spectrometry, 2009, v. 44, n. 7, p. 1047, doi. 10.1002/jms.1580
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The immunosuppressive activity and solution structures of ubiquitin fragments.
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- Biopolymers, 2009, v. 91, n. 6, p. 423, doi. 10.1002/bip.21160
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DNA Oxidative Cleavage Induced by the Novel Peptide Derivatives of 3-(quinoxalin-6-yl)alanine in Combination with Cu(II) or Fe(II) Ions.
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- Bioinorganic Chemistry & Applications, 2009, v. 2009, p. 1, doi. 10.1155/2009/906836
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