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<article article-type="research-article" dtd-version="1.3" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">chemicallytech</journal-id><journal-title-group><journal-title xml:lang="en">Fine Chemical Technologies</journal-title><trans-title-group xml:lang="ru"><trans-title>Тонкие химические технологии</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2410-6593</issn><issn pub-type="epub">2686-7575</issn><publisher><publisher-name>MIREA – Russian Technological University (RTU MIREA).</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.32362/2410-6593-2016-11-5-70-80</article-id><article-id custom-type="elpub" pub-id-type="custom">chemicallytech-51</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>CHEMISTRY AND TECHNOLOGY OF MEDICINAL COMPOUNDS AND BIOLOGICALLY ACTIVE SUBSTANCES</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>ХИМИЯ И ТЕХНОЛОГИЯ ЛЕКАРСТВЕННЫХ ПРЕПАРАТОВ И БИОЛОГИЧЕСКИ АКТИВНЫХ СОЕДИНЕНИЙ</subject></subj-group></article-categories><title-group><article-title>IDENTIFICATION OF EPO-Fс FUSION PROTEIN BY MEANS OF POLYACRYLAMIDE GEL-ELECTROPHORESIS WITH ISOELECTROFOCUSING (IEF-PAGE)AND IN PRESENCE OF SODIUM DODECYLSULPHATE (SDS-PAGE)/ LAUROYLSARCOSINATE (SAR-PAGE) FOR THE PURPOSE OF ANTI-DOPING CONTROL</article-title><trans-title-group xml:lang="ru"><trans-title>ИДЕНТИФИКАЦИЯ ГИБРИДНОГО БЕЛКА ЭПО-Fc МЕТОДАМИ ПОЛИАКРИЛАМИДНОГО ГЕЛЬ-ЭЛЕКТРОФОРЕЗА С ИЗОЭЛЕКТРИЧЕСКИМ ФОКУСИРОВАНЕИМ (IEF-PAGE) И В ПРИСУТСТВИИ ДОДЕЦИЛСУЛЬФАТА (SDS-PAGE)/ЛАУРИЛСАРКОЗИНАТА НАТРИЯ (SAR-PAGE) С ЦЕЛЬЮ АНТИДОПИНГОВОГО КОНТРОЛЯ</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Постников</surname><given-names>П. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Postnikov</surname><given-names>P. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>старший научный сотрудник отдела пептидного допинга и анализа крови</p><p> </p></bio><bio xml:lang="en"><p>Moscow, 105005 Russia</p></bio><email xlink:type="simple">horemxeb-haos@mail.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Кротов</surname><given-names>Г. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Krotov</surname><given-names>G. I.</given-names></name></name-alternatives><bio xml:lang="ru"><p>начальник отдела пептидного допинга и анализа крови</p><p> </p></bio><bio xml:lang="en"><p>Moscow, 105005 Russia</p></bio><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Ефимова</surname><given-names>Ю. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Efimova</surname><given-names>Yu. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>доцент</p><p>Москва, 119571 Россия</p></bio><bio xml:lang="en"><p>Moscow, 119571 Russia</p></bio><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Дикунец</surname><given-names>М. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Dikunets</surname><given-names>M. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>директор</p><p> </p></bio><bio xml:lang="en"><p>Moscow, 105005 Russia</p></bio><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Федеральное государственное бюджетное учреждение «Антидопинговый Центр»</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Federal State Budgetary Institution “Antidoping Centre”</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>Московский технологический университет (Институт тонких химических технологий)</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Moscow Technological University (Institute of Fine Chemical Technologies)</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2016</year></pub-date><pub-date pub-type="epub"><day>28</day><month>10</month><year>2016</year></pub-date><volume>11</volume><issue>5</issue><fpage>70</fpage><lpage>80</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Postnikov P.V., Krotov G.I., Efimova Y.A., Dikunets M.A., 2016</copyright-statement><copyright-year>2016</copyright-year><copyright-holder xml:lang="ru">Постников П.В., Кротов Г.И., Ефимова Ю.А., Дикунец М.А.</copyright-holder><copyright-holder xml:lang="en">Postnikov P.V., Krotov G.I., Efimova Y.A., Dikunets M.A.</copyright-holder><license xml:lang="ru" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>Данная работа распространяется под лицензией Creative Commons Attribution 4.0.</license-p></license><license xml:lang="en" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>This work is licensed under a Creative Commons Attribution 4.0 License.</license-p></license></permissions><self-uri xlink:href="https://www.finechem-mirea.ru/jour/article/view/51">https://www.finechem-mirea.ru/jour/article/view/51</self-uri><abstract><p>The article is devoted to develop of an approach for the identification of new stimulator of ematopoiesis, EPO-Fc fusion protein, which is banned by the World Anti-doping Agency (WADA) to use by athletes since it has become doping. Existing methods of qualitative determination of this substances in routine practice of antidoping laboratories such as polyacrylamide gelelectrophoresis in presence of sodium dodecylsulphate (SDS-PAGE) or lauroylsarcosinate (SARPAGE) are insufficiently specific. The article shows the principal possibility of identification of EPO-Fc fusion protein by means of IEF-PAGE in carrier ampholyte-based gels with a pH range 2-6 after Fc-fragment removal via fermentative hydrolysis.It has been shown that the removing of the crystallizable fragment leads to decrease of molecular weight of whole hybrid molecule and to increase its electrophoretic mobility that allows to detect this banned substances with high specificity by existing methods. During the study the enzyme for hydrolytic cleavage and optimum conditions of hydrolysis of EPO-Fc in serum samples were selected.</p></abstract><trans-abstract xml:lang="ru"><p>Статья посвящена разработке подхода по идентификации нового стимулятора кроветворения, гибридного белка ЭПО-Fc, запрещенного Всемирным антидопинговым агентством (ВАДА) для употребления спортсменами и являющегося допингом. Существующие в рутинной практике антидопинговых лабораторий мира методы качественного определения данного вещества с помощью полиакриламидного гель-электрофореза в присутствии додецилсульфата (SDS-PAGE) и лаурилсаркозината (SAR-PAGE) натрия недостаточно специфичны. В статье описана принципиальная возможность идентификации ЭПО-Fc методом изоэлектрического фокусирования в полиакриламидном геле (IEF-PAGE) с градиентом рН 2-6 после удаления Fc-части молекулы посредством ферментативного гидролиза. Показано, что удаление кристаллизуемого фрагмента приводит к уменьшению молекулярной массы всей гибридной молекулы и увеличению ее электрофоретической подвижности, что позволяет специфично детектировать запрещенное вещество существующими методами. В ходе исследования выбран фермент для гидролитического расщепления ЭПО-Fc и подобраны оптимальные условия гидролиза в образцах сыворотки крови.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>гибридный белок ЭПО-Fc</kwd><kwd>ферментативный гидролиз</kwd><kwd>электрофорез</kwd><kwd>фрагмент ЭПО-шарнир</kwd><kwd>антидопинговый контроль</kwd></kwd-group><kwd-group xml:lang="en"><kwd>fermentative hydrolysis</kwd><kwd>EPO-Fc fusion protein</kwd><kwd>electrophoresis</kwd><kwd>EPO-hinge fragment</kwd><kwd>antidoping control</kwd></kwd-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Bitonti A.J., Dumont J.A., Low S.C., Peters R.T., Kropp K.E., Palombella V. J., Stattel J. M., Lu Y., Tan C.A., Song J.J., Garcia A.M., Simister N.E., Spiekermann G.M., Lencer W.I., Blumberg R.S. // Proc. Natl. Acad. Sci. USA. 2004. V. 101. Is. 26. 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