Structure and self-assembly of the influenza matrix protein M1 in solution after virion destruction.

2018

  1. Konarev PV, Svergun DI (2018) Direct shape determination of intermediates in evolving macromolecular solutions from small-angle scattering data. IUCrJ 5(Pt 4):402-409. doi: 10.1107/S2052252518005900 (Q1)
  2. Cordeiro M, Otrelo-Cardoso AR, Svergun DI, Konarev PV, Lima JC, Santos-Silva T, Baptista PV (2018) Optical and Structural Characterization of a Chronic Myeloid Leukemia DNA Biosensor. ACS Chem Biol doi: 10.1021/acschembio.8b00029 (Q1)

  3. Adinolfi S, Puglisi R, Crack JC, Iannuzzi C, Dal Piaz F, Konarev PV, Svergun DI, Martin S, Le Brun NE, Pastore A (2018) The Molecular Bases of the Dual Regulation of Bacterial Iron Sulfur Cluster Biogenesis by CyaY and IscX. Front Mol Biosci 4:97. doi: 10.3389/fmolb.2017.00097 (Q1)

  4. Aronsson A, Güler F, Petoukhov MV, Crennell SJ, Svergun DI, Linares-Pastén JA, Karlsson EN (2018) Structural insights of RmXyn10A - A prebiotic-producing GH10 xylanase with a non-conserved aglycone binding region. Biochim. Biophys. Acta doi: 10.1016/j.bbapap.2017.11.006 (Q1)

  5. Nataliia Aleksandrova, Irina Gutsche, Eaazhisai Kandiah, Sergiy V. Avilov, Maxim V. Petoukhov, Elena Seiradake, Andrew A. McCarthy (2018) Robo1 Forms a Compact Dimer-of-Dimers Assembly. Structure. V. 26. P. 1-9. doi.org/10.1016/j.str.2017.12.003 (Q1)

  6. Larisa V. Kordyukova, Eleonora V. Shtykova, Lyudmila A. Baratova, Dmitri I. Svergun & Oleg V. Batishchev (2018) Matrix proteins of enveloped viruses: a case study of Influenza A virus M1 protein. Journal of Biomolecular Structure and Dynamics. doi: 10.1080/07391102.2018.1436089.(Q3)

2017

  1. E. V. Shtykova, L. A. Dadinova, N. V. Fedorova, A. E. Golanikov, E. N. Bogacheva, A. L. Ksenofontov, L. A. Baratova, L. A. Shilova, V. Yu. Tashkin, T. R. Galimzyanov, C. M. Jeffries, D. I. Svergun & O. V. Batishchev (2017) Influenza virus Matrix Protein M1 preserves its conformation with pH, changing multimerization state at the priming stage due to electrostatics. Scientific Reports 7, 16793. doi:10.1038/s41598-017-16986-y.

  2. Ksenofontov Alexander L., Dobrov Eugeny N., Fedorova Natalia V., Serebryakova Marina V., Prusov Andrey N., Baratova Ludmila A., Viiu Paalme, Lilian Järvekülg, Shtykova Eleonora V. Isolated Potato Virus A coat protein possesses unusual properties and forms different short virus-like particles. Journal of Biomolecular Structure and Dynamics. 2017, http://dx.doi.org/10.1080/07391102.2017.1333457.

  3. Victor A. Radyukhin, Liubov A. Dadinova, Ivan A. Orlov & Ludmila A. Baratova. Amphipathic secondary structure elements and putative cholesterol recognizing amino acid consensus (CRAC) motifs as governing factors of highly specific matrix protein interactions with raft-type membranes in enveloped viruses. (2017) Journal of Biomolecular Structure and Dynamics, https://doi.org/10.1080/07391102.2017.1323012.

  4. Yevdokimov Y. M., Skuridin S. G., Semenov S. V., Dadinova L. A., Salyanov V. I., Kats E. I. Re-entrant cholesteric phase in DNA liquid-crystalline dispersion particles.(2017) J. Biol. Phys., 43, p. 45–68. doi: 10.1007/s10867-016-9433-4.

  5. Holdbrook DA, Burmann BM, Huber RG, Petoukhov MV, Svergun DI, Hiller S, Bond PJ (2017) A Spring-Loaded Mechanism Governs the Clamp-like Dynamics of the Skp Chaperone. 25: 1079-1088 e3.

  6. Franke D, Petoukhov M V., Konarev P V., Panjkovich A, Tuukkanen A, Mertens HDT, Kikhney AG, Hajizadeh NR, Franklin JM, Jeffries CM, Svergun DI (2017) ATSAS 2.8 : a comprehensive data analysis suite for small-angle scattering from macromolecular solutions. J. Appl. Crystallogr. 50: 1151–1158.

  7. A.S: Boikova, Y.A. Dyakova, K.B. Ilina, P.V. Konarev, A.E. Kryukova, A.I. Kuklin, M.A. Marchenkova, B.V. Nabatov, A.E. Blagov, Y.V. Pisarevsky, and M. V. Kovalchuk (2017) Octamer formation in lysozyme solutions at the initial crystallization stage detected by small-angle neutron scattering Acta Cryst. D, 73, 591-599. DOI: 10.1134/S1063774517060074.

  8. S.K. Filippov, B. Verbraeken, P.V. Konarev, D.I. Svergun, B. Angelov, N.S. Vishnevetskaya, C.M. Papadakis, S. Rogers, A. Radulescu, T. Courtin, J.C. Martins, L. Starovoytova, M. Hruby, P. Stepanek, V.S. Kravchenko, I.I. Potemkin, R. Hoogenboom (2017) Block and Gradient Copoly(2-oxazoline) Micelles: Strikingly Different on the Inside J Phys Chem Lett. 8, 3800-3804. DOI: 10.1021/acs.jpclett.7b01588.

  9. S. Covaceuszach, M. Bozzi, M.G. Bigotti, F. Sciandra, P.V. Konarev, A. Brancaccio, A. Cassetta (2017) The effect of the pathological V72I, D109N and T190M missense mutations on the molecular structure of α-dystroglycan PLoS One 12, e0186110.doi: 10.1371/journal.pone.0186110.

  10. В.В. Волков, В.В. Дмитриев, Д.В. Золотухин, А.А. Солдатов, А.Н. Юдин. Метод получения образцов упорядоченного аэрогеля различной плотности. Приборы и техника эксперимента.   2017.   № 5.   С.130–135.

  11. D.O. Shvedchenko, V.V. Volkov, E.I. Suvorova. Sizes and size distributions of nanoparticles: Causes of differences in results obtained by transmission electron microscopy and small angle X-ray scattering. Nanosystems: Physics, Chemistry, Mathematics.   2017.   8(4).   P.512–522.

  12. Л. А. Шилова, Д. Г. Князев, Н. В. Федорова, Э. В. Штыкова, О. В. Батищев. Изучение адсорбции матриксного белка М1 вируса гриппа на липидных мембранах методом флуоресцентных зондов. Биологические мембраны, 2017, 34(3), с. 194-200.

  13. Margarita S. Rubina, Alexander Yu. Vasil’kov, Alexander V. Naumkin, Eleonora V. Shtykova, Sergey S. Abramchuk, Mousa A. Alghuthaymi, Kamel A. Abd-Elsalam. Synthesis and characterization of chitosan–copper nanocomposites and their fungicidal activity against two sclerotia-forming plant pathogenic fungi. J Nanostruct Chem., 2017, published online 21 July 2017, DOI 10.1007/s40097-017-0235-4.

  14. Э. В. Штыкова, Е. Н. Богачева, Л. А. Дадинова, С. М. Джеффрис, Н. В. Федорова, А. О. Головко, Л. А. Баратова, О. В. Батищев. Малоугловое рентгеновское исследование строения макромолекул. Структура белка NS2 (NEP) в растворе. Кристаллография, 2017, том 62, № 6, с. 907-916.

  15. Kamel A. Abd-Elsalam,  Alexander Yu. Vasil’kov, Ernest E. Said-Galiev, Margarita S. Rubina, Alexei R. Khokhlov,  AlexanderV. Naumkin, Eleonora V. Shtykova,  Mousa A. Alghuthaymi. Bimetallic blends and chitosan nanocomposites: novel antifungal agents against cotton seedling damping-off. Eur J Plant Pathol, 2017. Published online 02 October 2017.   DOI 10.1007/s10658-017-1349-8.

2016

  1. L. A. Dadinova, E. V. Shtykova, P.V. Konarev, E. V. Rodina, N. E. Snalina, N. N. Vorobyeva, S. A. Kurilova, T. I. Nazarova, C.M. Jeffries, D. I. Svergun.  X-Ray Solution Scattering Study of Four Escherichia coli Enzymes Involved in Stationary-Phase Metabolism. PLoS One, 2016, 11(5): e0156105. doi:10.1371/journal.pone.0156105.

  2. Boer DR, Ruiz-Masó JA, Rueda M, Petoukhov MV, Machón C, Svergun DI, Orozco M, Del Solar G, Coll M. (2016) Conformational plasticity of RepB, the replication initiator protein of promiscuous streptococcal plasmid pMV158. Sci Rep 6:20915, doi:10.1038/srep20915.

  3. Hastings, R., de Villiers, C., Hooper, C., Ormondroyd, L., Pagnamenta, A., Lise, S., Salatino, S., Knight, S.J., Taylor, J.C., Thomson, K.L., Arnold, L., Chatziefthimiou, S.D., Konarev, P.V., Wilmanns, M., Ehler, E., Ghisleni, A., Gautel, M., Blair, E., Watkins, H., Gehmlich, K. (2016) Combination of Whole Genome Sequencing, Linkage and Functional Studies Implicates a Missense Mutation in Titin as a Cause of Autosomal Dominant Cardiomyopathy with Features of Left Ventricular Non-Compaction. Circ Cardiovasc Genet., 9, 426-435. DOI: 10.1161/CIRCGENETICS.116.001431.

  4. Konarev, P.V., Petoukhov, M.V., Svergun, D.I. (2016) Rapid automated superposition of shapes and macromolecular models using spherical harmonics. J. Appl Crystallogr. 49, 953-960. DOI: 10.1107/S1600576716005793.

  5. Konarev, P.V., Volkov, V.V., Svergun, D.I. (2016) Interactive graphical system for small-angle scattering analysis of polydisperse systems. Journal of Physics: Conference Series, 747, e012036. DOI: 10.1088/1742-6596/747/1/012036.

  6. Т. П. Логинова, Г. И. Тимофеева, О. Л. Лепендина, В. А. Шандинцев, А. А. Матюшин, И. А. Хотина, Э. В. Штыкова. Получение и исследование свойств наночастиц магнетита в гибридных мицеллах полистирол-блок-полиэтиленоксида и додецилсульфата натрия. Кристаллография, 2016, 61 (1), сс. 86-92.

  7. Дадинова Л.А., Родина Е.В., Воробьева Н.Н., Курилова С.А., Назарова Т.И., Штыкова Э.В. Структурные исследования дигидролипоилдегидрогеназы из E. сoli в растворе: малоугловое рентгеновское рассеяние и молекулярный докинг. Кристаллография, 2016, том 61, № 3, с. 406-412.

  8. Yuri M. Yevdokimov, Sergey G. Skuridin, Viktor I. Salyanov, Eleonora V. Shtykova, Nicolai G. Khlebtsov, Efim I. Kats. The gold nanoparticles influence the spatial ordering of double-stranded nucleic acid molecules. Front Nanosci Nanotech, 2016, 2(3): 135-143, doi: 10.15761/FNN.1000124.

  9. Э.В. Штыкова, Л.А. Фейгин, В.В. Волков, Ю.Н. Малахова, А.И. Бузин, С.Н. Чвалун, Катаржнова Е.Ю, Игнатьева Г.М., А.М. Музафаров. Малоугловое рентгеновское исследование строения полимеров. Карбосилановые дендримеры в растворе гексана. Кристаллография, 2016, том 61, № 5, с. 781-792.

  10. М.А. Марченкова, В.В. Волков, А.Е. Благов, Ю.А. Дьякова, К.Б. Ильина, Е.Ю Терещенко., В.И. Тимофеев, Ю.В. Писаревский, М.В. Ковальчук. In situ-исследования состояния молекул лизоцима на стадии начала процесса кристаллизации методом малоуглового рентгеновского рассеяния. Кристаллография. – 2016. – Т. 61. – №1. – С.10-15.

2015

  1. W. Wang, E. V. Shtykova, V. V. Volkov, G. Chang, L. Zhang, Y. Dong,  P. Liu. Influence of polychromaticity on particle structure determination in small-angle X-ray scattering. J. Appl. Cryst., 2015, 48, 1935-1942, doi:10.1107/S1600576715019214.

  2. Petoukhov MV, Svergun DI (2015) Ambiguity assessment of small-angle scattering curves from monodisperse systems. Acta Cryst. D71, 1051-1058.

  3. Ponnusamy R, Petoukhov MV, Correia B, Custodio TF, Juillard F, Tan M, Pires de Miranda M, Carrondo MA, Simas JP, Kaye KM, Svergun DI, McVey CE (2015) KSHV but not MHV-68 LANA induces a strong bend upon binding to terminal repeat viral DNA. Nucleic Acids Res. 43(20), 10039-54.

  4. Konarev, P.V., Svergun, D.I. (2015) A posteriori determination of the useful data range for small-angle scattering experiments on dilute monodisperse systems. IUCr Journal, 2, 352-360. DOI: 10.1107/S2052252515005163.

  5. Malyutin, A.G., Cheng, H., Sanchez-Felix, O.R., Carlson, K.R., Stein, B.D., Konarev, P.V., Svergun, D.I., Dragnea, B., Bronstein, L.M. (2015) Coat protein-dependent behavior of poly(ethylene glycol) tails in iron oxide core virus-like nanoparticles. ACS Appl Mater Interfaces. 7, 12089-12098.DOI: 10.1021/acsami.5b02278

  6. Song, J.G., Kostan, J., Drepper, F., Knapp, B., de Almeida Ribeiro, E. Jr,, Konarev, P.V., Grishkovskaya, I.,Wiche, G., Gregor, M., Svergun, D.I., Warscheid, B., Djinović-Carugo, K. (2015) Structural Insights into Ca(2+)-Calmodulin Regulation of Plectin 1a-Integrin β4 Interaction in Hemidesmosomes. Structure 23, 558-570. DOI: 10.1016/j.str.2015.01.011.

  7. Covaceuszach ,S., Konarev, P.V., Cassetta, A., Paoletti, F., Svergun, D.I., Lamba, D., Cattaneo, A. (2015) The conundrum of the high-affinity NGF binding site formation unveiled? Biophys J. 108, 687-697. DOI: 10.1016/j.bpj.2014.11.3485.

  8. V. Kochervinskii, I. Malyshkina, A. Pavlov, N. Bessonova, A. Korlyukov, V. Volkov, N. Kozlova, N. Shmakova. Influence of parameters of molecular mobility on formation of structure in ferroelectric vinylidene fluoride copolymers. J. Appl. Phys. –  2015. V.117. – P.214101-1 - P.214101-9.  – doi: 10.1063/1.4921851.

  9. В.Е. Асадчиков, Р.Ш. Асхадуллин, В.В. Волков, В. В. Дмитриев, Н.К. Китаева, П.Н. Мартынов, А.А. Осипов, А.А. Сенин, А.А. Солдатов, Д.И. Чекрыгина, А.Н. Юдин. Структура и свойства “нематически упорядоченных” аэрогелей Письма в ЖЭТФ. – 2015. – Т.101. – Вып.8. – С.613 – 619.

  10. Ю.М. Евдокимов, В.И. Салянов, С.Г. Скуридин, Э.В. Штыкова, Н.Г. Хлебцов, Е.И. Кац.  Физико-химический и нанотехнологический подходы к созданию «твердых» пространственных структур ДНК. Успехи химии, 2015, 84 (1), с. 27- 42.

  11. Э.В.Штыкова. Восстановление структуры низкого разрешения полидисперсных и полиморфных нанообъектов по данным малоуглового рассеяния (компьютерное моделирование). Российские нанотехнологии, 2015, 10, (5-6), 60 - 70.

  12. Yevdokimov Yu. M., Skuridin S.G., Salyanov V.I., Shtykova E.V., Dadinova L.A., Volkov V.V.., Khlebtsov N.G., Komarov P.V., Kats E. Negatively Charged Gold Nanoparticles “Control” Double-Stranded DNAs Spatial Packing. Journal of Materials Science & Nanotechnology, 2015, 3 (2): 201.

2014

  1. Petoukhov MV, Weissenhorn W, Svergun DI (2014) Endophilin-A1 BAR domain interaction with arachidonyl CoA. Frontiers in Molecular Biosciences October 2014, Volume 1, Article 20: 1-8. doi: 10.3389/fmolb.2014.00020.

  2. Malecki, P. H., Vorgias, C. E., Petoukhov, M. V., Svergun, D. I., and Rypniewski, W. (2014) Crystal structures of substrate-bound chitinase from the psychrophilic bacterium Moritella marina and its structure in solution, Acta Crystallogr D Biol Crystallogr 70, 676-684.

  3. Konarev P.V., Kachalova G.S., Ryazanova A.Y., Kubareva E.A., Karyagina A.S., Bartunik H.D., Svergun D.I.(2014) Flexibility of the Linker between the Domains of DNA Methyltransferase SsoII Revealed by Small-Angle X-Ray Scattering: Implications for Transcription Regulation in SsoII Restriction–Modification System. PLoS ONE 9(4):e93453. DOI: 10.1371/journal.pone.0093453.

  4. Duelli A, Kiss B, Lundholm I, Bodor A, Petoukhov MV, Svergun DI, Nyitray L, Katona G (2014) The C-terminal random coil region tunes the Ca(2)(+)-binding affinity of S100A4 through conformational activation. Plos One 9: e97654.

  5. de Almeida Ribeiro, E., Pinotsis, N., Ghisleni, A., Salmazo, A., Konarev, P.V., Kostan, J., Sjoeblom, B.,Schreiner, C., Polyansky, A.A.,Gkougkoulia, E.A., Holt, M.R., Aachmann, F.L., Žagrović, B., Bordignon, E., Pirker, K.F., Svergun, D.I., Gautel, M., Djinović-Carugo1, K. (2014) The structure of human muscle α-actinin: Insight into regulation and Z-disk assembly. Cell, 159, 1-14.DOI: 10.1016/j.cell.2014.10.056.

  6. Ю.М. Евдокимов, С.Г. Скуридин, В.И. Салянов, В.И. Попенко, Э.В. Штыкова, Л.А.Дадинова,  В.В. Волков, Н.Г. Хлебцов, Б.Н. Хлебцов, Е.И. Кац. Новый нанобиоматериал – частицы жидкокристаллических дисперсий ДНК со встроенными кластерами из наночастиц золота. Российские нанотехнологии, 2014, 9, N3-4, сс. 82-89.

  7. L. Jiao, S. Ouyang, N. Shaw, G. Song, Y. Feng, F. Niu, W. Qiu, H. Zhu, L.-W. Hung, X. Zuo, E. Shtykova, P. Zhu, Yu. Dong, R. Xu, Z.-J. Liu.  Mechanism of the Rpn13-induced activation of Uch37. Protein Cell 2014, 5 (8), 616-630 DOI: 10.1007/s13238-014-0046-z.

  8. Ю.М. Евдокимов, В.И. Салянов, Э.В. Штыкова, Е.И. Кац, Н.Г. Хлебцов, С.Г. Скуридин. Структурная нанотехнология нуклеиновых кислот: создание «жидких» и «твердых» наноконструкций ДНК. Вестник Российской академии наук, 2014, том 84, № 8, с. 694-707.

  9. A.V. Pastukhov, V.A. Davankov, V.V. Volkov, S.V. Amarantov, K.I. Lubentsova. Structure and sorption properties of hypercrosslinked polystyrenes and magnetic nanocomposite materials based on them. J. Polym. Res. – 2014. – P.1-11. – DOI 10.1007/s10965-014-0406-7.

  10. Yu. M. Yevdokimov, V. I. Salyanov, E. V. Shtykova, N. G. Khlebtsov, E. I. Kats, S. G. Skuridin. The Physicochemical and Nanotechnological Approaches to Creation of “Rigid” DNA Nanoconstructions. The Open Nanoscience Journal, 2014, 8, 1-12.

2013

  1. Wenjia Wang,  Haifeng Hou, Qian Du, Wen Zhang, Guangfeng Liu, Eleonora V. Shtykova, Jianhua Xu, Peng Liu, and Yuhui Dong. Solution SAXS studies of RecQ from Deinococcus radiodurans and its complexes with junction DNA substrates. J. Biol. Chem. 288: 32414-32423 published September 25, 2013 as DOI:10.1074/jbc.M113.502112

  2. Eleonora V. Shtykova, Yuri A. Kabachii, Pyotr M. Valetsky, Sergey S. Kochev, Andrey G. Malyutin, Barry D. Stein, Lyudmila M. Bronstein, Dmitri I. Svergun. Solution Study of Novel Diblock Copolymers: Morphology and Structural Transition. Polymer
    2013, 54 (26), 6971-6978.

  3. Э.В.Штыкова. Малоугловое рассеяние, нано, грипп, etc…, Природа, 2013, 11, С. 28-36.

  4. Eleonora V. Shtykova, Lyudmila A. Baratova, Natalia V. Fedorova, Victor  A. Radyukhin, Alexander L. Ksenofontov, Vladimir V. Volkov,  Alexander V. Shishkov, Alexey A. Dolgov, Oleg V. Batishchev, Cy M. Jeffries, Dmitri I. Svergun. Structural Analysis of Influenza A Virus Matrix Protein M1 and Its Self-Assemblies at Low pH. PLoS One, 2013, Published December 16, 2013, e82431. doi:10.1371/journal.pone.0082431.

  5. Wenjia Wang, Qiong Guo, Eleonora V. Shtykova, Guangfeng Liu, Jianhua Xu, Maikun Teng, Peng Liu, Yuhui Dong. Structural peculiarities of the (MHF1-MHF2)4 octamer provide a long DNA binding patch to anchor the MHF-FANCM complex to chromatin: a solution SAXS study. FEBS Letters, 2013, V. 587, N 18, pp.2912-2917.

  6. Petoukhov, M. V., Billas, I. M., Takacs, M., Graewert, M. A., Moras, D., and Svergun, D. I. (2013) Reconstruction of Quaternary Structure from X-ray Scattering by Equilibrium Mixtures of Biological Macromolecules, Biochemistry 52, 6844-6855.

  7. Groothuizen, F. S., Fish, A., Petoukhov, M. V., Reumer, A., Manelyte, L., Winterwerp, H. H., Marinus, M. G., Lebbink, J. H., Svergun, D. I., Friedhoff, P., and Sixma, T. K. (2013) Using stable MutS dimers and tetramers to quantitatively analyze DNA mismatch recognition and sliding clamp formation, Nucleic Acids Res 41, 8166-8181.

  8. Filippov S.K., Franklin J.M., Konarev P.V., Chytil P., Etrych T., Bogomolova A., Dyakonova M., Papadakis, C.M., Radulescu A., Ulbrich K., Stepanek P., Svergun D.I. (2013) Hydrolytically degradable polymer micelles for drug delivery: A SAXS/SANS kinetic study. Biomacromolecules. 14, 4061-4070. DOI:10.1021/bm401186z

  9. Nowak E., Potrzebowski W., Konarev P.V., Rausch J.W., Bona M.K., Svergun D.I., Bujnicki J.M., Le Grice, S.F., Nowotny M. (2013) Structural analysis of monomeric retroviral reverse transcriptase in complex with an RNA/DNA hybrid. Nucleic Acids Res 41, 3874-3887. DOI: 10.1093/nar/gkt053.

  10. V. V. Volkov, V. A. Lapuk, D. I. Chekrygina, E. Yu. Varlamova, A. V. Chekushin. Difference between conformations of immunoglobulin M and human rheumatoid factor based on small-angle X-ray solution scattering data. Mendeleev Comm. – 2013. – T. 23. – P.319-320.

  11. А.С. Авилов, М.А. Ермакова, Ю.А. Кузин, В.А. Митюхляев, П.А. Тодуа, В.В. Волков, Ю.А. Дьякова, М.А. Запорожец, М.А. Марченкова, С.Н. Сульянов, Д.И. Чекрыгина, С.П. Губин, Е.Г. Рустамова.  Метрологическое обеспечение измерений размерных параметров наночастици тонких пленок методами малоугловой рентгеновской дифрактометрии. Российские нанотехнологии. – 2013. — Т. 8. — № 5. – С. 30-36.

2012

  1. Petoukhov MV, Franke D, Shkumatov AV, Tria G, Kikhney AG, Gajda M, Gorba C, Mertens HDT, Konarev PV, Svergun DI (2012) New developments in the ATSAS program package for small-angle scattering data analysis. Journal of Applied Crystallography, 45, 342-350.

  2. Shtykova, E. V.; Kuchkina, N. V.; Shifrina, Z. B.; Bronstein, L. M.; Svergun, D. I., Unusual Structural Morphology of Dendrimer/CdS Nanocomposites Revealed by Synchrotron X-ray Scattering. J. Phys. Chem. C (2012), 116, 8069–8078, Cover paper.

  3. Ying Liu, Zeng-Qiang Gao, Zhun She, Kun Qu, Wen-Jia Wang, Eleonora V Shtykova, Jian-Hua Xu, Chao-Neng Ji, Yu-Hui Dong, The structural basis of the response regulator DrRRA from Deinococcus radiodurans. Biochem Biophys Res Commun. (2012), Jan 27; 417(4):1206-12.

  4. Vladimir V. Volkov, Victor A. Lapuk, Anna I. Toropova, Elena Yu. Varlamova, Eleonora V. Shtykova,  Kirill A. Dembo,  Vladimir P. Timofeev, A comparative study of immunoglobulin IgM and rheumatoid factor IgMRF in solution by small-angle X-ray scattering.  Mendeleev Commun., (2012), 22, 159-161, Cover paper.

  5. Heng Zhang, Zeng-Qiang Gao, Wen-Jia Wang, Guang-Feng Liu, Eleonora V. Shtykova, Jian-Hua Xu, Lan-Fen Li, Xiao-Dong Su, Yu-Hui Dong, The crystal structure of the MPN domain from the COP9 signalosome subunit CSN6. FEBS Letters, 586 (2012) 1147–1153.

  6. Yong Wei, Heng Zhang, Zeng-Qiang Gao, Wen-Jia Wang, Eleonora V. Shtykova , Jian-Hua Xu, Quan-Sheng Liu and Yu-Hui Dong, Crystal and Solution Structures of Methyltransferase RsmH Provide Basis for Methylation of C1402 in 16S rRNA. Journal of Structural Biology, (2012),  179, Issue 1, July 2012, Pages 29–40.

  7. Heng Zhang; Zeng-Qiang  Gao; Yong  Wei; Wen-Jia Wang; Guang-Feng Liu; Eleonora Shtykova; Jian-Hua  Xu; Yu-Hui Dong. Insights into the Catalytic Mechanism of 16S rRNA Methyltransferase RsmE (m3U1498) from Crystal and Solution Structures. Journal of Molecular Biology, (2012), 423, 576–589.

  8. Heng Zhang, Zeng-Qiang Gao, Yong Wei, Wen-Jia Wang, Guang-Feng Liu, Eleonora V. Shtykova,  Jian-Hua Xu, Yu-Hui Dong. Structural insights into the function of 23S rRNA methyltransferase RlmG (m2G1835) from Escherichia coli. RNA, (2012), 18 (8), doi:10.1261/rna.033407.112. 

  9. Zhun She,   Zeng-Qiang Gao,   Ying Liu,   Wen-Jia Wang,   Guang-Feng Liu,   Eleonora V. Shtykova,   Jian-Hua Xu,   Yu-Hui Dong. Structural and SAXS analysis of the budding yeast SHU-complex proteins. FEBS Letters, (2012), V. 586 (16), pp. 2306–2312.

  10. Саид-Галиев Э.Е., Васильков А.Ю., Николаев А.Ю., Лисицын А.И., Наумкин А.В., Волков И.О., Абрамчук С.С., Лепендина О.Л., Хохлов А.Р., Штыкова Э.В., Дембо К.А.  Cтруктура моно- и биметаллических гетерогенных катализаторов на основе благородных металлов, полученных с помощью флюидной технологии и металло-парового синтеза. Журнал физической химии,  2012, 86, No. 10, сс 1706–1713.

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