کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
10548034 | 965411 | 2005 | 10 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Production of milligram quantities of affinity tagged-proteins using automated multistep chromatographic purification
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موضوعات مرتبط
مهندسی و علوم پایه
شیمی
شیمی آنالیزی یا شیمی تجزیه
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چکیده انگلیسی
A new chromatography system, ÃKTAxpress (GE Healthcare, Amersham Biosciences, Uppsala, Sweden) has been designed to meet the demand for high-throughput purification of proteins in structural genomics and drug discovery. The system offers a number of automated multistep purification protocols for affinity-tagged proteins. All protocols start with affinity chromatography followed by combinations of desalting, ion exchange chromatography and gel filtration. As an option, tag removal can be included in the purification protocols. Up to 16 proteins can be purified per day and the yield can be as high as 50Â mg of each protein at >90% purity. To highlight the versatility of the system, this paper presents several case studies; purifications of hexahistidine- and glutathione S-transferase-tagged proteins using different protocols, automated on-column tag cleavage and optimization studies for a hexahistidine-tagged kinase.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Chromatography A - Volume 1080, Issue 1, 1 July 2005, Pages 83-92
Journal: Journal of Chromatography A - Volume 1080, Issue 1, 1 July 2005, Pages 83-92
نویسندگان
Rama Bhikhabhai, Anna Sjöberg, Lotta Hedkvist, Markus Galin, Pia Liljedahl, Tuomo FrigÃ¥rd, Niklas Pettersson, Mats Nilsson, Jill A. Sigrell-Simon, Christine Markeland-Johansson,