Title of article :
Immobilised metal-ion affinity chromatography purification of histidine-tagged recombinant proteins: a wash step with a low concentration of EDTA
Author/Authors :
Westra، نويسنده , , Douwe F. and Welling، نويسنده , , Gjalt W. and Koedijk، نويسنده , , Danny G.A.M. and Scheffer، نويسنده , , Albert Jan and Smit، نويسنده , , T.Hauw and Welling-Wester، نويسنده , , Sytske Welling-Wester، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2001
Pages :
8
From page :
129
To page :
136
Abstract :
Immobilised metal-ion affinity chromatography (IMAC) is widely used for the purification of recombinant proteins in which a poly-histidine tag is introduced. However, other proteins may also bind to IMAC columns. We describe the use of a washing buffer with a low concentration of EDTA (0.5 mM) for the removal of proteins without histidine tag from IMAC columns. Four histidine-tagged recombinant proteins/protein complexes were purified to homogeneity from cell culture medium of insect cells by using an EDTA washing buffer. The presence of a low concentration of EDTA in washing buffers during IMAC may have a general application in the purification of histidine-tagged proteins.
Keywords :
recombinant proteins , histidine , EDTA
Journal title :
Journal of Chromatography B Biomedical Sciences and Applications
Serial Year :
2001
Journal title :
Journal of Chromatography B Biomedical Sciences and Applications
Record number :
1705612
Link To Document :
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