کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1201144 1493615 2013 10 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Analytical characterization of complex, biotechnological feedstocks by pH gradient ion exchange chromatography for purification process development
موضوعات مرتبط
مهندسی و علوم پایه شیمی شیمی آنالیزی یا شیمی تجزیه
پیش نمایش صفحه اول مقاله
Analytical characterization of complex, biotechnological feedstocks by pH gradient ion exchange chromatography for purification process development
چکیده انگلیسی


• Multidimensional analysis to characterize complex biotechnological feedstocks.
• pH gradient IEC is used to fractionate a lysate containing a diagnostic protein.
• Fractions are analysed by Dot-Blot and SDS PAGE.
• The relevant contaminants are defined and subsequently identified using LC–MS.
• Obtained information is used to lay out purification of the target protein by IEC.

The accelerating growth of the market for proteins and the growing interest in new, more complex molecules are bringing new challenges to the downstream process development of these proteins. This results in a demand for faster, more cost efficient, and highly understood downstream processes. Screening procedures based on high-throughput methods are widely applied nowadays to develop purification processes for proteins. However, screening highly complex biotechnological feedstocks, such as complete cell lysates containing target proteins often expressed with a low titre, is still very challenging. In this work we demonstrate a multidimensional, analytical screening approach based on pH gradient ion exchange chromatography (IEC), gel electrophoresis and protein identification via mass spectrometry to rationally characterize a biotechnological feedstock for the purpose of purification process development. With this very simple characterization strategy a two-step purification based on consecutive IEC operations was rapidly laid out for the purification of a diagnostic protein from a cell lysate reaching a purity of ∼80%. The target protein was recombinantly produced using an insect cell expression system.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Chromatography A - Volume 1311, 11 October 2013, Pages 55–64
نویسندگان
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