Abstract
Expressed protein ligation is a valuable method for protein semisynthesis that involves the reaction of recombinant protein C-terminal thioesters with N-terminal cysteine (N-Cys)-containing peptides, but the requirement of a Cys residue at the ligation junction can limit the utility of this method. Here we employ subtiligase variants to efficiently ligate Cys-free peptides to protein thioesters. Using this method, we have more accurately determined the effect of C-terminal phosphorylation on the tumor suppressor protein PTEN.
MeSH terms
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Animals
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Bacillus subtilis / enzymology
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Bacillus subtilis / genetics
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Blotting, Western
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Catalytic Domain
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Cells, Cultured
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Cysteine / chemistry
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Escherichia coli / enzymology
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Escherichia coli / genetics
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Fibroblasts / metabolism
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Mice
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Mutagenesis, Site-Directed
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PTEN Phosphohydrolase / chemical synthesis*
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PTEN Phosphohydrolase / chemistry
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PTEN Phosphohydrolase / genetics
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Peptide Fragments / chemical synthesis*
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Peptide Fragments / chemistry
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Peptide Fragments / genetics
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Peptide Synthases / chemistry*
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Peptide Synthases / genetics
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Phosphorylation
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Protein Processing, Post-Translational
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Recombinant Proteins / chemical synthesis*
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Recombinant Proteins / chemistry
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Recombinant Proteins / genetics
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Subtilisins / chemistry*
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Subtilisins / genetics
Substances
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Peptide Fragments
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Recombinant Proteins
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PTEN Phosphohydrolase
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Subtilisins
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Peptide Synthases
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subtiligase
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Cysteine