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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="ru"><front><journal-meta><journal-id journal-id-type="publisher-id">scbmt</journal-id><journal-title-group><journal-title xml:lang="ru">БИОМЕДИЦИНА</journal-title><trans-title-group xml:lang="en"><trans-title>Journal Biomed</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2074-5982</issn><issn pub-type="epub">2713-0428</issn><publisher><publisher-name>Scientific center of biomedical technologies of Federal Medical and Biological Agency</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.33647/2074-5982-18-3-14-17</article-id><article-id custom-type="elpub" pub-id-type="custom">scbmt-1402</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="ru"><subject>МЕТОДЫ И ТЕХНОЛОГИИ БИОМЕДИЦИНСКИХ ИССЛЕДОВАНИЙ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>METHODS AND TECHNOLOGIES OF BIOMEDICAL RESEARCH</subject></subj-group></article-categories><title-group><article-title>Оценка одиночных нуклеотидных полиморфизмов человеческого сывороточного альбумина, ассоциированных с болезнью Альцгеймера</article-title><trans-title-group xml:lang="en"><trans-title>Evaluation of Single-Nucleotide Polymorphisms in Human Serum Albumin Associated with Alzheimer's Disease</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>Дерюшева</surname><given-names>Е. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Deryusheva</surname><given-names>E. I.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Дерюшева Евгения Игоревна - кандидат физико-математических наук.</p><p>142290, Московская обл., Пущино, просп. Науки, 3.</p></bio><bio xml:lang="en"><p>Evgeniya I. Deryusheva - Cand. Sci. (Phis.-Math.), Federal Research Center “Pushchino Scientific Center for Biological Research of the Russian Academy of Sciences”.</p><p>142290, Moscow Region, Pushchino, Nauki Ave., 3.</p></bio><email xlink:type="simple">evgenia.deryusheva@gmail.com</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>Литус</surname><given-names>Е. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Litus</surname><given-names>E. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Литус Екатерина Андреевна - кандидат медицинских наук.</p><p>142290, Московская обл., Пущино, просп. Науки, 3.</p></bio><bio xml:lang="en"><p>Ekaterina A. Litus - Cand. Sci. (Med.), Federal Research Center “Pushchino Scientific Center for Biological Research of the Russian Academy of Sciences”.</p><p>142290, Moscow Region, Pushchino, Nauki Ave., 3.</p></bio><email xlink:type="simple">ealitus@gmail.com</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>ФГБУН «Федеральный исследовательский центр «Пущинский научный центр биологических исследований РAH»</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Federal Research Center “Pushchino Scientific Center for Biological Research of the Russian Academy of Sciences”</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2022</year></pub-date><pub-date pub-type="epub"><day>16</day><month>10</month><year>2022</year></pub-date><volume>18</volume><issue>3</issue><fpage>14</fpage><lpage>17</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Дерюшева Е.И., Литус Е.А., 2022</copyright-statement><copyright-year>2022</copyright-year><copyright-holder xml:lang="ru">Дерюшева Е.И., Литус Е.А.</copyright-holder><copyright-holder xml:lang="en">Deryusheva E.I., Litus E.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://journal.scbmt.ru/jour/article/view/1402">https://journal.scbmt.ru/jour/article/view/1402</self-uri><abstract><p>Человеческий сывороточный альбумин (ЧСА) является природным буфером амилоидного β-пептида (Аβ), ключевого фактора развития болезни Альцгеймера (БА). Увеличение сродства ЧСА к Aβ может достигаться путём насыщения ЧСА низкомолекулярными лигандами, такими как серотонин, отдельные жирные кислоты. Анализ геномных данных экзомов (WES), ассоциированных с БА (база данных ADSP), выявил наличие однонуклеотидного полиморфизма гена ЧСА в центрах связывания ибупрофена, арахидоновой и олеиновой кислот. Исследование свойств найденных генетических вариантов ЧСА позволит определить варианты, восприимчивые к модулирующему воздействию лигандов ЧСА, повышающих его сродство к Аβ.</p></abstract><trans-abstract xml:lang="en"><p>Human serum albumin (HSA) is a natural buffer for amyloid в peptide (Аβ), which is a key factor in the development of Alzheimer's disease (AD). An increase in HSA affinity to Аβ can be achieved via HSA saturation with low-molecular-weight ligands, such as serotonin or specific fatty acids. The conducted analysis of the genomic data of exomes (WES) associated with AD (ADSP database) revealed the presence of a single-nucleotide polymorphism of the HSA gene at the binding sites of ibuprofen, arachidonic and oleic acids. Research into the properties of the revealed genetic variants of HSA should be carried out to determine those variants that are susceptible to the modulatory action of HSA ligands, thus increasing its affinity to Aβ.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>однонуклеотидный полиморфизм</kwd><kwd>человеческий сывороточный альбумин</kwd><kwd>болезнь Альцгеймера</kwd></kwd-group><kwd-group xml:lang="en"><kwd>single nucleotide polymorphism</kwd><kwd>human serum albumin</kwd><kwd>Alzheimer's disease</kwd></kwd-group><funding-group><funding-statement xml:lang="ru">Исследование выполнено при финансовой поддержке Российского научного фонда, грант № 20-74-10072.</funding-statement><funding-statement xml:lang="en">Research was funded by a grant from the Russian Science Foundation, No. 20-74-10072.</funding-statement></funding-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Amtul Z., Uhrig M., Wang L., Rozmahel R.F., Beyreuther K. 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