| Literature DB >> 24508590 |
J McGraw1, V K Tatipelli1, O Feyijinmi1, M C Traore1, P Eangoor1, S Lane1, E J Stollar2.
Abstract
A growing number of studies require the purification of multiple proteins simultaneously and the development of simple economical high-throughput purification methods is essential. We have tested the purification of two related proteins in a variety of conditions to benchmark the semi-automated affinity chromatography method for the QIAcube that we have developed. We find that this new QIAcube method can successfully purify milligram quantities of proteins with minimal user involvement and performs as well as methods based on gravity. The method could easily be adapted to other chromatography resins and should prove to be a versatile method for optimizing protein expression or purification conditions for multiple proteins while obtaining sufficient amounts for subsequent biochemical analyses.Entities:
Keywords: High-throughput automation; Protein expression; Protein purification; QIAcube; SH3 domain
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Year: 2014 PMID: 24508590 PMCID: PMC4287359 DOI: 10.1016/j.pep.2014.01.014
Source DB: PubMed Journal: Protein Expr Purif ISSN: 1046-5928 Impact factor: 1.650