An affinity-based strategy for the design of selective displacers for the chromatographic separation of proteins

We describe an affinity-based strategy for designing selective protein displacers for the chromatographic purification of proteins. To design a displacer that is selective for a target protein, we attached a component with affinity for the target protein to a resin-binding component; we then tested...

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Veröffentlicht in:Langmuir : the ACS journal of surfaces and colloids. - 1992. - 24(2008), 13 vom: 01. Juni, Seite 6768-73
1. Verfasser: Vutukuru, Srinavya (VerfasserIn)
Weitere Verfasser: Kate, Sandesh D, McCallum, Scott A, Morrison, Christopher J, Cramer, Steven M, Kane, Ravi S
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2008
Zugriff auf das übergeordnete Werk:Langmuir : the ACS journal of surfaces and colloids
Schlagworte:Journal Article Research Support, Non-U.S. Gov't Proteins Avidin 1405-69-2 Biotin 6SO6U10H04 Aprotinin 9087-70-1 Muramidase EC 3.2.1.17
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500 |a Date Revised 21.11.2013 
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500 |a Citation Status MEDLINE 
520 |a We describe an affinity-based strategy for designing selective protein displacers for the chromatographic purification of proteins. To design a displacer that is selective for a target protein, we attached a component with affinity for the target protein to a resin-binding component; we then tested the ability of such displacers to selectively retain the target protein on a resin relative to another protein having a similar retention time. In particular, we synthesized displacers based on biotin, which selectively retained avidin as compared to aprotinin on SP Sepharose high performance resin. In addition, we have extended this approach to develop an affinity-peptide-based displacer that discriminates between lysozyme and cytochrome c. Here, a selective displacer was designed from a lysozyme-binding peptide that had been identified and optimized previously using phage-display technology. Our results suggest a general strategy for designing highly selective affinity-based displacers by identifying molecules (e.g., peptides) that bind to a protein of interest and using an appropriate linker to attach these molecules to a moiety that binds to the stationary phase 
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650 4 |a Research Support, Non-U.S. Gov't 
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650 7 |a 6SO6U10H04  |2 NLM 
650 7 |a Aprotinin  |2 NLM 
650 7 |a 9087-70-1  |2 NLM 
650 7 |a Muramidase  |2 NLM 
650 7 |a EC 3.2.1.17  |2 NLM 
700 1 |a Kate, Sandesh D  |e verfasserin  |4 aut 
700 1 |a McCallum, Scott A  |e verfasserin  |4 aut 
700 1 |a Morrison, Christopher J  |e verfasserin  |4 aut 
700 1 |a Cramer, Steven M  |e verfasserin  |4 aut 
700 1 |a Kane, Ravi S  |e verfasserin  |4 aut 
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