Разработка метода получения и очистки CEdG для молекулярных и биологических исследований

Разработка метода получения и очистки CEdG для молекулярных и биологических исследований

Bibliographic Details
Parent link:Перспективы развития фундаментальных наук=Prospects of fundamental sciences development: сборник научных трудов XI Международной конференция студентов и молодых ученых, г. Томск, 22-25 апреля 2014 г./ Национальный исследовательский Томский политехнический университет (ТПУ) ; под ред. Е. А. Вайтулевич. [С. 305-307].— , 2014
Main Author: Богданов А. О.
Corporate Author: Национальный исследовательский Томский политехнический университет (ТПУ) Институт природных ресурсов (ИПР) Кафедра технологии органических веществ и полимерных материалов (ТОВПМ)
Other Authors: Кривощеков С. В. Сергей Владимирович, Дементьева Н. Б.
Summary:Заглавие с экрана
Methylglyoxal (MG) is a high reactive compound and it is one of the damaging environmental factors. Methylglyoxal presents in micromolar quantities in many food products and in most biological fluids of different organisms, it is known that increasing of MG level has a mutagenic effect in vivo [1]. MG is capable of reacting with nucleophilic groups in proteins, lipids and DNA, forming covalent compounds also known as advanced glycation end products. Protein glycation end products have been characterized well and it was shown that these adducts play a role in various pathological processes, such as diabetes mellitus [2], cancer, degenerative conditions associated with aging [3] Alzheimer's disease. DNA glycation end products can be used as potential markers of different pathological processes. N2-carboxyethyl-2'-deoxyguanosine is one of the compounds which formed during the reaction of methylglyoxal or glucose with double-stranded DNA in vitro [5].The aim of the research was to synthesize of N2-carboxyethyl -2'-deoxyguanosine as a standard substance for molecular studies of the DNA glycation in the socially significant diseases pathogenesis. We propose a new method for purifying N2-carboxyethyl-2'-deoxyguanosine from the reaction mixture by reversed-phase HPLC.
Published: 2014
Series:Химия
Subjects:
электронный ресурс
труды учёных ТПУ
очистка
молекулярные исследования
биологические исследования
метилглиоксаль
Online Access:http://www.lib.tpu.ru/fulltext/c/2014/C21/098.pdf
Format: Electronic Book Chapter
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=606906

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