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<article 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" xmlns:ali="http://www.niso.org/schemas/ali/1.0/" article-type="review-article" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Acta Naturae</journal-id><journal-title-group><journal-title xml:lang="en">Acta Naturae</journal-title><trans-title-group xml:lang="ru"><trans-title>Acta Naturae</trans-title></trans-title-group></journal-title-group><issn publication-format="print">2075-8251</issn><publisher><publisher-name xml:lang="en">Acta Naturae Ltd</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">11545</article-id><article-id pub-id-type="doi">10.32607/actanaturae.11545</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>Reviews</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>Обзоры</subject></subj-group><subj-group subj-group-type="article-type"><subject>Review Article</subject></subj-group></article-categories><title-group><article-title xml:lang="en">Artificial Scaffold PolypeptidesAs an Efficient Tool for the Targeted Delivery of Nanostructures In Vitro and In Vivo</article-title><trans-title-group xml:lang="ru"><trans-title>Распознающие cкаффолдовые полипептиды как инструмент для адресной доставки наноструктур in vitro и in vivo</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Shipunova</surname><given-names>Victoria O.</given-names></name><name xml:lang="ru"><surname>Шипунова</surname><given-names>Виктория Олеговна</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><email>viktoriya.shipunova@phystech.edu</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Deyev</surname><given-names>Sergey M.</given-names></name><name xml:lang="ru"><surname>Деев</surname><given-names>Сергей Михайлович</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><email>viktoriya.shipunova@phystech.edu</email><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry of the Russian Academy of Sciences</institution></aff><aff><institution xml:lang="ru">Институт биоорганической химии им. академиков М.М. Шемякина и Ю.А. Овчинникова РАН</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2022-05-10" publication-format="electronic"><day>10</day><month>05</month><year>2022</year></pub-date><volume>14</volume><issue>1</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>54</fpage><lpage>72</lpage><history><date date-type="received" iso-8601-date="2021-08-04"><day>04</day><month>08</month><year>2021</year></date><date date-type="accepted" iso-8601-date="2022-02-11"><day>11</day><month>02</month><year>2022</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2022, Shipunova V.O., Deyev S.M.</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2022, Шипунова В.О., Деев С.М.</copyright-statement><copyright-year>2022</copyright-year><copyright-holder xml:lang="en">Shipunova V.O., Deyev S.M.</copyright-holder><copyright-holder xml:lang="ru">Шипунова В.О., Деев С.М.</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/><license><ali:license_ref xmlns:ali="http://www.niso.org/schemas/ali/1.0/">https://creativecommons.org/licenses/by/4.0</ali:license_ref></license></permissions><self-uri xlink:href="https://actanaturae.ru/2075-8251/article/view/11545">https://actanaturae.ru/2075-8251/article/view/11545</self-uri><abstract xml:lang="en"><p>The use of traditional tools for the targeted delivery of nanostructures, such as antibodies, transferrin, lectins, or aptamers, often leads to an entire range of undesirable effects. The large size of antibodies often does not allow one to reach the required number of molecules on the surface of nanostructures during modification, and the constant domains of heavy chains, due to their effector functions, can induce phagocytosis. In the recent two decades, targeted polypeptide scaffold molecules of a non-immunoglobulin nature, antibody mimetics, have emerged as much more effective targeting tools. They are small in size (3–20 kDa), possess high affinity (from subnano- to femtomolar binding constants), low immunogenicity, and exceptional thermodynamic stability. These molecules can be effectively produced in bacterial cells, and, using genetic engineering manipulations, it is possible to create multispecific fusion proteins for the targeting of nanoparticles to cells with a given molecular portrait, which makes scaffold polypeptides an optimal tool for theranostics.</p></abstract><trans-abstract xml:lang="ru"><p>Традиционные средства адресной доставки наноструктур, такие, как антитела, трансферрин, лектины или аптамеры, зачастую могут вызывать целый спектр нежелательных эффектов. При этом большой размер антител часто не позволяет разместить необходимое количество молекул на поверхности наноструктур, а константные домены тяжелых цепей, благодаря их эффекторным функциям, могут вызывать фагоцитоз. В последние два десятилетия гораздо более эффективными инструментами для направленной доставки считаются миметики антител – адресные полипептидные скаффолдовые (каркасные) молекулы неиммуноглобулиновой природы. Они обладают малым размером (3–20 кДа), высокой аффинностью (от субнано- до фемтомолярных значений констант связывания), низкой иммуногенностью, исключительной термодинамической стабильностью. Эти молекулы эффективно нарабатывают в бактериальных продуцентах и с помощью генно-инженерных манипуляций создают мультиспецифичные белки слияния для нацеливания наночастиц на клетки с заданным молекулярным профилем, что делает скаффолдовые полипептиды оптимальным средством для тераностики.</p></trans-abstract><kwd-group xml:lang="en"><kwd>nanoparticles</kwd><kwd>DARPins</kwd><kwd>affibody</kwd><kwd>anticalins</kwd><kwd>scaffold proteins</kwd><kwd>ADAPT</kwd><kwd>HER2</kwd><kwd>HER1</kwd><kwd>EGFR</kwd><kwd>EpCAM</kwd><kwd>conjugation</kwd><kwd>targeted delivery</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>наночастицы</kwd><kwd>дарпины</kwd><kwd>аффибоди</kwd><kwd>антикалины</kwd><kwd>каркасные белки</kwd><kwd>ADAPT</kwd><kwd>HER2</kwd><kwd>HER1</kwd><kwd>EGFR</kwd><kwd>EpCAM</kwd><kwd>конъюгация</kwd><kwd>адресная доставка</kwd></kwd-group><funding-group><award-group><funding-source><institution-wrap><institution xml:lang="ru">РФФИ</institution></institution-wrap><institution-wrap><institution xml:lang="en">Russian Foundation for Basic Research</institution></institution-wrap></funding-source><award-id>20-14-50514</award-id></award-group><funding-statement xml:lang="en">The study was carried out with the financial support of the Russian Foundation for Basic Research, project No. 20-14-50514.</funding-statement><funding-statement xml:lang="ru">Исследование выполнено при финансовой поддержке РФФИ в рамках научного проекта № 20-14-50514.</funding-statement></funding-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><citation-alternatives><mixed-citation xml:lang="en">Deyev S.M., Lebedenko E.N. // Russ. 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