Analytical characterization of complex, biotechnological feedstocks by pH gradient ion exchange chromatography for purification process development
| Autor: | Martijn W. H. Pinkse, Beckley K. Nfor, Marcel Ottens, Peter Verhaert, Alexander T. Hanke, Frieder Kröner, Jürgen Hubbuch |
|---|---|
| Rok vydání: | 2013 |
| Předmět: |
Gel electrophoresis
Insecta Lysis Chromatography Chemistry Organic Chemistry Ion chromatography Proteins RNA-Binding Proteins General Medicine Hydrogen-Ion Concentration Chromatography Ion Exchange Phosphoproteins Mass spectrometry Biochemistry Recombinant Proteins Cell Line Analytical Chemistry Characterization (materials science) Protein purification Animals Humans Electrophoresis Polyacrylamide Gel Target protein Screening procedures |
| Zdroj: | Journal of Chromatography A. 1311:55-64 |
| ISSN: | 0021-9673 |
| DOI: | 10.1016/j.chroma.2013.08.034 |
| Popis: | 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. |
| Databáze: | OpenAIRE |
| Externí odkaz: |
|
Full Text from ScienceDirect