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Scale-up protein separation on stainless steel wide bore toroidal columns in the type-J counter-current chromatography.

Journal of chromatography. A (2015-03-31)
Yue Hugh Guan, Peter Hewitson, Remco N A M van den Heuvel, Yan Zhao, Rick P G Siebers, Ying-Ping Zhuang, Ian Sutherland
RESUMEN

Manufacturing high-value added biotech biopharmaceutical products (e.g. therapeutic proteins) requires quick-to-develop, GMP-compliant, easy-to-scale and cost effective preparatory chromatography technologies. In this work, we describe the construction and testing of a set of 5-mm inner diameter stainless steel toroidal columns for use on commercially available preparatory scale synchronous J-type counter-current chromatography (CCC) machinery. We used a 20.2m long column with an aqueous two-phase system containing 14% (w/w) PEG1000 and 14% (w/w) potassium phosphate at pH 7, and tested a sample loading of 5% column volume and a mobile phase flow rate of 20ml/min. We then satisfactorily demonstrated the potential for a weekly protein separation and preparation throughput of ca. 11g based on a normal weekly routine for separating a pair of model proteins by making five stacked injections on a single portion of stationary phase with no stripping. Compared to our previous 1.6mm bore PTFE toroidal column, the present columns enlarged the nominal column processing throughput by nearly 10. For an ideal model protein injection modality, we observed a scaling up factor of at least 21. The 2 scales of protein separation and purification steps were realized on the same commercial CCC device.

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Sigma-Aldrich
Fosfato de potasio monobasic, ACS reagent, ≥99.0%
Sigma-Aldrich
Fosfato de potasio dibasic, ACS reagent, ≥98%
Sigma-Aldrich
Lisozima from chicken egg white, powder or granules, ≥90 %, ≥39,000 units/mg protein
Sigma-Aldrich
Myoglobin from equine skeletal muscle, 95-100%, essentially salt-free, lyophilized powder
Sigma-Aldrich
Poli(etilenglicol), average Mn 950-1,050