Аффилиация
a Уральский государственный экономический университет, Екатеринбург
b Уральский государственный экономический университет, Yekaterinburg
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http://creativecommons.org/licenses/by/4.0/), позволяет другим распространять, перерабатывать, исправлять и развивать произведение, даже в коммерческих целях, при условии указания автора произведения.
Аннотация
Пептиды являются потенциально перспективными аналогами синтетических лекарственных препаратов для лечения гиперурикемии. Цель исследования – идентифицировать устойчивые аминокислотные паттерны, обуславливающие ингибирующую ксантиноксидазную активность пептидов, предложить на их основе новые антигиперурикемические пептиды с доказанной посредством использования методологии пред иктивной аналитики in silico эффективностью. Объектами исследования являлись пептиды, обладающие ингибирующей ксантиноксидазной активностью. В работе применялась авторская программа поиска, идентификации и количественной оценки повторяющихся сочетаний аминокислотных остатков в целевых пептидных последовательностях. Проводили оценку физико-химических и фармакокинетических свойств, ингибирующей ксантиноксидазной активности, общей и целевой биологической активности, а также токсичности идентифицированных пептидов. Количество аминокислот в цепи, изоэлектрическая точка, заряд при нейтральном pH, молекулярная масса пептидов и индекс гидрофобности были рассчитаны теоретически.
Идентифицированы аминокислотные паттерны, ответственные за процесс ингибирования фермента ксантиноксидазы, сгенерированы новые пептидные последовательности. Идентифицированы 49 нетоксичных пептидов с различной длиной аминокислотной последовательности, обладающих потенциально высокой антимикробной и ингибирующей активностью в отношении целевых мишеней лекарственных препаратов, используемых при гиперурикемии и сахарном диабете 2 типа. Пептиды охарактеризовали как низкомолекулярные соединения гидрофильной (преимущественно) и гидрофобной природы длиной от 4 до 7 аминокислот, содержащие в структуре преимущественно аминокислотные остатки пролина, триптофана и фенилаланина со средней молекулярной массой 723 Да и отрицательным зарядом.
Результаты данного исследования являются важным шагом в понимании молекулярных механизмов ингибирования фермента ксантиноксидазы и открывают новые перспективы для разработки антигиперурикемических пептидных препаратов.
Ключевые слова
Пептиды,
гиперурикемия,
ингибиторы ксантиноксидазы,
аминокислотные паттерны,
IC50
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