Literature DB >> 19498977

Automated high-throughput purification of 6xHis-tagged proteins.

Frank Schafer1, Ulla Römer, Melanie Emmerlich, Julia Blümer, Helge Lubenow, Kerstin Steinert.   

Abstract

Methods based on immobilized-metal affinity chromatography (IMAC) technology for the isolation of 6xHis-tagged proteins offer a one-step purification process that is both robust and meets the challenge of quantitatively purifying thousands of proteins with differing structures and characteristics. To perform this method in a high-throughput, automated format, protocols have been developed that can be run on lab automation workstations. Ready-to-run protocols covering a wide range of protein purification and assay applications, and which rely on the well-established 6xHis-Ni-NTA IMAC technology, are available. An Ni-NTA magnetic bead-based protocol allows micro-scale purification of up to 15 microg of 6xHis-tagged protein per well. If larger amounts of purified protein are needed, a vacuum-controlled Ni-NTA resin-based process provides a convenient medium-scale method for purification of up to 300 microg of 6xHis-tagged protein in a 96-well format. This protocol has been adapted to further increase the yield of 6xHis-tagged proteins allowing purification of up to several milligrams of highly pure protein per well. The protocol can process 96 samples, each derived from up to 25 mL culture volume (E. coli), in less than 3 h. Examples of purification and assay applications using the protocols mentioned above, and data on reproducibility and cross-contamination-free processing are shown.

Entities:  

Year:  2002        PMID: 19498977      PMCID: PMC2279864     

Source DB:  PubMed          Journal:  J Biomol Tech        ISSN: 1524-0215


  28 in total

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Journal:  Protein Eng       Date:  1997-08

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Journal:  Biotechniques       Date:  1994-04       Impact factor: 1.993

4.  Identification of vaccine candidates against serogroup B meningococcus by whole-genome sequencing.

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Journal:  Science       Date:  2000-03-10       Impact factor: 47.728

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Authors:  R Felleisen; V Zimmermann; B Gottstein; N Müller
Journal:  Biotechniques       Date:  1996-04       Impact factor: 1.993

6.  pALEX, a dual-tag prokaryotic expression vector for the purification of full-length proteins.

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Journal:  Gene       Date:  1995-10-16       Impact factor: 3.688

7.  New metal chelate adsorbent selective for proteins and peptides containing neighbouring histidine residues.

Authors:  E Hochuli; H Döbeli; A Schacher
Journal:  J Chromatogr       Date:  1987-12-18

8.  Physiological inhibitors of the catalytic subunit of cAMP-dependent protein kinase: effect of MgATP on protein-protein interactions.

Authors:  F W Herberg; S S Taylor
Journal:  Biochemistry       Date:  1993-12-21       Impact factor: 3.162

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Authors:  T G Schmidt; J Koepke; R Frank; A Skerra
Journal:  J Mol Biol       Date:  1996-02-09       Impact factor: 5.469

10.  Identification and functional analysis of chaperonin 10, the groES homolog from yeast mitochondria.

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Journal:  Proc Natl Acad Sci U S A       Date:  1993-12-01       Impact factor: 11.205

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Journal:  Biomagn Res Technol       Date:  2004-11-26

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Authors:  Gro Elin Kjæreng Bjerga; Adele Kim Williamson
Journal:  BMC Biotechnol       Date:  2015-08-19       Impact factor: 2.563

4.  Generation of a vector suite for protein solubility screening.

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  4 in total

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