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Application of a Novel CL7/Im7 Affinity System in Purification of Complex and Pharmaceutical Proteins

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Affinity Chromatography

Part of the book series: Methods in Molecular Biology ((MIMB,volume 2466))

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Abstract

We have developed the CL7/Im7 protein purification system to achieve high-yield, high-purity and high-activity (HHH) products in one step. The system is based on the natural ultrahigh-affinity complex between the two small proteins encoded by colicinogenic plasmids carried by certain E. coli strains, the DNAse domain of colicin E7 (CE7; MW ~ 15 kDa) and its natural endogenous inhibitor, the immunity protein 7 (Im7; MW ~ 10 kDa). CL7 is an engineered variant of CE7, in which the toxic DNA-binding and catalytic activities have been eliminated while retaining the high affinity to Im7. CL7 is used as a protein tag, while Im7 is covalently attached to agarose beads. To make the CL7/Im7 technique easy to use, we have designed a set of the E. coli expression vectors for fusion of a target protein to the protease-cleavable CL7-tag either at the N- or the C-terminus, and also have the options of the dual (CL7/His8) tag. A subset of vectors is dedicated for cloning membrane and multisubunit proteins. The CL7/Im7 system has several notable advatantages over other available affinity purification techniques. First, high concentrations of the small Im7 protein are coupled to the beads resulting in the high column capacities (up to 60 mg/mL). Second, an exceptional stability of Im7 allows for multiple (100+) regeneration cycles with no loss of binding capacities. Third, the CL7-tag improves protein expression levels, solubility and, in some cases, assists folding of the target proteins. Fourth, the on-column proteolytic elution produces purified proteins with few or no extra amino acid residues. Finally, the CL7/Im7 affinity is largely insensitive to high salt concentrations. For many target proteins, loading the bacterial lysates on the Im7 column in high salt is a key to high purity. Altogether, these properties of the CL7/Im7 system allow for a one-step HHH purification of most challenging, biologically and clinically significant proteins.

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Acknowledgments

This work was supported in part by the grant from TriAltus Bioscience to D.G.V and the University of Alabama at Birmingham. Louise Chow is supported by funds from an Anderson Family Endowed Chair through UAB.

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Authors and Affiliations

  1. Department of Biochemistry and Molecular Genetics, Schools of Medicine and Dentistry, University of Alabama at Birmingham, Birmingham, AL, USA

    Louise T. Chow & Dmitry G. Vassylyev

Authors
  1. Louise T. Chow
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  2. Dmitry G. Vassylyev
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Correspondence to Dmitry G. Vassylyev .

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Editors and Affiliations

  1. Molecular Virology and Microbiology, Baylor College of Medicine, Houston, TX, USA

    B. Vijayalakshmi Ayyar

  2. Astero Erado Inc, Houston, TX, USA

    Sushrut Arora

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Chow, L.T., Vassylyev, D.G. (2022). Application of a Novel CL7/Im7 Affinity System in Purification of Complex and Pharmaceutical Proteins. In: Ayyar, B.V., Arora, S. (eds) Affinity Chromatography. Methods in Molecular Biology, vol 2466. Humana, New York, NY. https://doi.org/10.1007/978-1-0716-2176-9_5

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  • DOI: https://doi.org/10.1007/978-1-0716-2176-9_5

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  • Publisher Name: Humana, New York, NY

  • Print ISBN: 978-1-0716-2175-2

  • Online ISBN: 978-1-0716-2176-9

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