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A convenient method for affinity purification of maltose binding protein fusions
Journal of Biotechnology, 1998Maltose binding protein of Escherichia coli is frequently employed as a fusion partner for the biosynthesis of polypeptides and proteins, largely because of the advantage provided by affinity purification of such a fusion. A mixture of cellulose and starch is shown to be a simple and effective alternative to the use of other, more complicated media ...
Usha Srinivasan, Jeffrey A. Bell
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Strategy for purifying maltose binding protein fusion proteins by affinity precipitation
Journal of Chromatography A, 2008The maltose binding protein (MBP) affinity tag has been extensively used for protein purification. A commercial grade cationic starch could precipitate MBP or an MBP-tagged protein quantitatively by simultaneous addition of 10% (w/v) polyethylene glycol (PEG) and 50 mM calcium chloride.
Raghava, Smita+4 more
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Folding and aggregation of export-defective mutants of the maltose-binding protein
Research in Microbiology, 2002We previously characterized a defective-folding variant of the periplasmic maltose-binding protein, MalE31. To examine the alternative folding pathways open to the MalE31 precursor, we have analyzed the cellular fates of this aggregation-prone protein carrying altered signal sequences.
Sabine Hunke+2 more
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Tritium NMR spectroscopy of ligand binding to maltose-binding protein
Biochemistry, 1991Tritium-labeled alpha- and beta-maltodextrins have been used to study their complexes with maltose-binding protein (MBP), a 40-kDa bacterial protein. Five substrates, from maltose to maltohexaose, were labeled at their reducing ends and their binding studied.
Philip G. Williams+4 more
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Associative properties of the Escherichiacoli galactose binding protein and maltose binding protein
Biochemical and Biophysical Research Communications, 1982The ligand-binding characteristics of periplasmic galactose-binding protein and maltose-binding protein of Escherichia coli are analyzed. The saturation function was decreased upon increasing protein concentration and the monomer-dimer equilibrium was shifted towards the monomeric protein form upon an increase of the ligand concentration.
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Purification of Proteins Fused to Maltose-Binding Protein.
Methods in molecular biology, 2017M. Lebendiker, T. Danieli
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Maltose-Binding Protein as a Solubility Enhancer
2003Jeffrey D. Fox, David S. Waugh
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Proteins: Structure, Function, and Bioinformatics, 2013
N. M. Mascarenhas, J. Kästner
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N. M. Mascarenhas, J. Kästner
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