کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1985581 1540230 2016 10 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Effects of macromolecular crowding and osmolyte on human Tau fibrillation
ترجمه فارسی عنوان
اثرات تراکم ماکرو مولکولی و اسمولیت بر فیبریلاسیون انسان تاو
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی زیست شیمی
چکیده انگلیسی


• Both Ficoll 70 and Dextran 70 can promote the fibrillation of human Tau protein.
• Dextran 70 has stronger enhancing effect on Tau fibrillation than Ficoll 70.
• Sucrose inhibits the enhancing effect of macromolecular crowding agents.

Tau fibrillation is reported to be involved in neurodegenerative disorders, such as Alzheimer's disease, in which the natural environment is very crowded in the cells. Understanding the role of crowding environments in regulating Tau fibrillation is of great importance for elucidating the etiology of these diseases. In this experiment, the effects of macromolecular crowding and osmolyte reagents in the crowding environment on Tau fibrillation were studied by thioflavin T binding, SDS-PAGE and TEM assays. Ficoll 70 and Dextran 70 of different concentrations were used as macromolecular crowding reagents inside the cells and showed a strong enhancing effect on the fibrillation of normal and hyperphosphorylated Tau. The enhancing effect of Dextran is stronger than that of Ficoll 70 at the same concentration. In addition, the cellular osmolyte sucrose was found to protect Tau against fibrillation, and inhibit the enhancing effect of macromolecular crowding on Tau fibrillation. A possible model for the fibrillation process of Tau and the effect of macromolecular crowding and osmolyte on this process was proposed based on these experimental results. The information obtained from our study can enhance the understanding of how proteins aggregate and avoid aggregation in crowded physiological environments and might lead to a better understanding of the molecular mechanisms of Alzheimer's disease in vivo.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: International Journal of Biological Macromolecules - Volume 90, September 2016, Pages 27–36
نویسندگان
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