کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
2504810 | 1557471 | 2009 | 4 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
A simple and reproducible approach to characterize protein stability using rheology
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کلمات کلیدی
موضوعات مرتبط
علوم پزشکی و سلامت
داروسازی، سم شناسی و علوم دارویی
علوم دارویی
پیش نمایش صفحه اول مقاله
چکیده انگلیسی
As the utility of proteins in medical diagnosis and therapy becomes more fully realized, interest in characterizing proteins' stability continues to increase. This paper reports the merits of rheology as an approach to characterizing the stability of a model protein, immunoglobulin (IgG). A controlled-strain rotational rheometer equipped with parallel plates geometry was used to measure changes in the viscosity of an IgG buffer solution during a programmed temperature ramp. The results demonstrated that protein stability characterization is reproducible using the melting temperature (or unfolding temperature) of IgG (Tm = 73.6 ± 0.4 °C). We have also identified an irreversible minor transition occurring at a temperature of 40-60 °C, which we believe to be the partial unfolding of some protein structures. Finally, we have determined that adding sugar, an established protein stabilizer, to the IgG buffer solution significantly increases the protein's melting temperature. Our results show the power and simplicity of rheology as analytical tool for characterizing protein stability through the measurement of viscosity changes during thermal denaturation.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: International Journal of Pharmaceutics - Volume 374, Issues 1â2, 5 June 2009, Pages 1-4
Journal: International Journal of Pharmaceutics - Volume 374, Issues 1â2, 5 June 2009, Pages 1-4
نویسندگان
Changdeng Liu, Christophe Vailhe, Newton Samuel, Qiang Min,