Вплив температури на взаємодію поліетиленгліколю з мембранами та орієнтаційний порядок білків цитоскелета еритроцитів людини
The study identified discrepancies in the modification of erythrocyte membrane upon exposure to polyethylene glycol with a molecular weight of 1500 (PEG) at various temperatures (4 and 37 °C) using the fluorescent probe 4-(n-dimethylaminostyryl)-1-methylpyridinium-n-toluenesulfonate (DSM), as well a...
Збережено в:
| Дата: | 2026 |
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| Автори: | , |
| Формат: | Стаття |
| Мова: | Англійська |
| Опубліковано: |
Publishing House ‘Akademperiodyka’ of the National Academy of Sciences of Ukraine; Institute for Problems of Cryobiology and Cryomedicine
2026
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| Теми: | |
| Онлайн доступ: | https://cryo.org.ua/journal/index.php/probl-cryobiol-cryomed/article/view/2180 |
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| Назва журналу: | Problems of Cryobiology and Cryomedicine |
Репозитарії
Problems of Cryobiology and Cryomedicine| Резюме: | The study identified discrepancies in the modification of erythrocyte membrane upon exposure to polyethylene glycol with a molecular weight of 1500 (PEG) at various temperatures (4 and 37 °C) using the fluorescent probe 4-(n-dimethylaminostyryl)-1-methylpyridinium-n-toluenesulfonate (DSM), as well as alterations in the orientation order of proteins in the membrane-cytoskeleton complex using polarization microscopy. Exposure of erythrocytes to PEG at 37 °C caused complete disappearance of the hydrophobic component from the DSM fluorescent spectrum due to competition between PEG and DSM molecules for binding sites. Lowering the exposure temperature of cells to a cryoprotective agent (CPA) to 4 °C reduced the possibility of its hydrophobic contacts with cell membranes attested by the presence of the hydrophobic component in the DSM spectrum, although at a lower level than in the control. The decrease in hydrophobic contacts of PEG to membranes upon a lowering temperature at the stage of erythrocyte exposure to CPA provided retaining to a large extent the orientation order of the membrane cytoskeleton molecules both under the incubation process with CPA and after freeze–thawing of cells.
Probl Cryobiol Cryomed. 2026; 36(1): 16—26. |
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